After my recent setback at the oncologist office, I was not looking forward to my urology visit. OK, no one ever looks forward to their urology visit, not even the urologist (I mean, who wants to look at that all day long?). However, I was looking forward to it even less this time.
For anyone that hasn't had a urology appointment this is how a typical urology visit goes. No matter when you have been there last, there will always be an additional 312 pieces of paperwork to fill out, most of them involve digging through your wallet for various insurance cards, IDs, addresses of estranged relatives, etc. Right in the middle of the paperwork, they will call you back up to the counter and give you a cup. This is not for drinking out of, even though it is already personalized with your name on it. So then, you have to figure out what to do with all the contents of your billfold that are spread on the seat next to you to fill out page 188, paragragh H, subsection 22.3.1 of the form verifying that you read the Paperwork Reduction Act, while you go off to fill the cup.
Once in the restroom one of two things will happen. It doesn't matter how much you have "studied" for your urine test, there will still only be these two options. Option one, you stand there awkwardly with the cup in one hand, and..."it" in the other, like two gunslingers at high noon staring down each other, neither one willing to draw first. You will stay like this for 30-45 minutes waiting for the flow to begin, which will happen precisely when you hear the nurse out in the waiting room calling your name. Or the only other possibility is you start going immediately and your volume of output is approximately the same gallons per minute rate of Lake Erie flowing into Niagara, which is all well and good, until you realize you are holding a cup with the capacity to hold the juice from a single grape. At this point you have to decide, are you going to overflow on your hand or spray all over the room trying to set the cup down midstream. These are the only two outcomes to the second situation. Don't try to be a hero and think that you can pull off some great acrobatic move to save the sample and also keep the floor dry. That kind of cavalier attitude will only result in wet clothes and/or soggy paperwork.
Once you have been called back to the doctor's office, you will remain sequestered there for roughly two and a half hours. Around you will be pictures of kidney stones resembling medieval weapons...except with more spikes, disgusting diagrams of every genital malady known to man (and some animals), and cutaway anatomical models of sex organs that will make you never want to have sex again. You will sit here alone in the Office of Horrors until you finally get the urge to pee because you drank too much water for the "cup" and as soon as you pull out your phone to try to get your mind off of your situation, the doctor will walk in and assume you are taking pictures of the plastic cutaway penis.
It is at this time, the doctor will ask you questions having nothing to do with why you are there. "Do you have to urinate more frequently at night if there is a full moon? Have you ever tried to scratch the back of your knee with your elbow? Do penguins sweat? Do you like gladiator movies?" And if you are lucky, you drop your pants, get a quick slap and tickle, pull up your pants, and get charged a couple hundred dollars. However, I am going to issue a warning!!!
If you have a serious concern, by all means, now is the time to ask the doc about it. After all, it was my own insistence, after the nurse missed my cancer initially, that resulted in my cancer diagnosis. Other than that I have found the best thing to do is DO NOT ASK THE UROLOGIST ANY QUESTIONS!!! See, if it's time for a prostate exam, it's an important part of a male's health and we all need to unpucker and endure it. However, any added information or question for some reason results in a bonus prostate exam. I don't know if they get paid more per violation, or all the doctors have a bet, or what, but every question results in a buttsploration. "Doc, is it normal for your urine to be a little darker if you have been sweating a lot on a hot day?" DROP YOUR PANTS AND BEND YOUR KNEES! "Doctor, is just waking up once a week in the middle of the night to pee excessive?" HERE COMES THE BIRDIE!! "How's your golf swing coming, doc?" KEEP AN EYE ON YOUR BALL AND GET READY FOR THE FOLLOW THROUGH!!!!
It was for this reason that I decided NOT to ask when I would be done visiting him. After all, every other time I had been asked, I was always told that I would have to see him for the rest of my life, and the next thing I would hear is the snap of a rubber glove behind me. So as I my freshly lubricated buttocks swished their way to the front desk to make my next appointment, I was pleasantly surprised to be told that I wouldn't need to come back unless there was a problem! After all, I had already been devastated by the news a couple months earlier that I was not being released by the oncologist when originally planned. It seemed that following months of bad news from doctors, I finally heard something I wanted to hear...even if I was walking funny.
Now I just want to clarify one thing here, testicular exams and prostate exams are very important, and there is a peace of mind that one has after clear test (well, that comes after the initial shock). And even though I was released from my urologist I will continue to do self exams (testicular self exam, I am not flexible enough for the other) and will still be getting the scheduled exams from my family doctor, oncologist, dentist, butcher, and anyone else with a white coat on (at least it seems that way sometimes). But for now I can relax...without being told to relax and bend over...and celebrate graduating from one doctor and hopefully being that much closer to being a considered a cancer survivor and not a cancer patient.
Showing posts with label dealing with cancer. Show all posts
Showing posts with label dealing with cancer. Show all posts
Thursday, September 17, 2015
Tuesday, June 16, 2015
PTSD and Cancer?
Having recently completed a trip that I had planned for a while, one of my bosses asked me how it went. I told her how the trip had special significance to my cancer fight and how it took on a new meaning after not being released from oncology as I hoped, and I talked to her about how the trip affected me. I made the comment to her (also someone who fought her own cancer battle), I said "It's weird the way certain things trigger these memories and feelings, it's almost like PTSD." She replied "It is PTSD!"
Her words struck me as odd. I know people with PTSD, and some of them have a lot more to worry about than I do. After all I was basically disappointed that I have to keep going back to the doctor, that I'm still a cancer patient. That's all. Yes, there are certain triggers, certain things that cause memories to come flooding back, but that's just life. That happens with lots of things right? Every time I smell cow manure, I get flash backs to the county fair and start look for deep fried anything.
Later on that day, I just Googled "PTSD" and "cancer", thinking I would find a few anecdotes here, or casual observations there. What popped up on the page astounded me. Studies, LOTS of studies on the subject. And they all came to basically the same conclusion, it's not just in our heads...well it is, technically, I guess...but a lot of us are experiencing it.
There were tons of articles but the same results seemed to be popping up in every study. One out of every three of us experience this. It only shows up AFTER active treatment, usually when patients are in their monitoring stage. It can start as soon as 6 months after active treatment, but many experience it at about the three year mark. And the trigger to cause the onset of the effects doesn't necessarily have to be cancer related, but it brings back the cancer thoughts.
Before I go any further, I don't think I have "post traumatic stress disorder". As I mentioned, I know people that have PTSD, and I wouldn't even begin to compare my problem with theirs. However, I do have SOMETHING going on. And the research shows that clearly a lot more of us do too.
That's when I started getting a little angry. Further reading on the studies shows that very few oncologists even realize that this is going on.
For those that haven't been to an oncology monitoring appointment it goes like this, you sit in a sterile waiting room (literally, because chemo knocks out your immune system). You look at the pile of old hard candy (because chemo also dries out your mouth), trying to decide if you are desperate enough to get a piece. Then the phlebotomist calls you, puts you on the scale while you try to claim that your shoes weigh 50 pounds a piece, takes your vitals, and sucks out about 4 gallons of blood for various tests, spells, and incantations. Then, before they shuffle you off to wait in the oncologist office, they ask where you are on the pain scale, physically and mentally (you know that little scale of various emojis before they were emojis, ranging from happy face emoji to frowny crying face emoji). That's where it dawned on me when the breakdown was.
Going into my last oncology appointment, I was excited. I had my monitoring extended once, but had been told by everyone...except the oncologist, that this would probably be my last appointment ever. When asked where I was psychologically, I picked a "3" out of "10" ("10" being the most stressed). After I was told to continue monitoring I was absolutely devastated. Had anyone stopped me on the way out the door and asked me to give my number on that scale again, it would have been an "8" or a "9". This was the failure. This is where no one is paying attention. And I don't necessarily blame the oncologists. Like many of the studies discovered, oncologist are trained to fight cancer, not delve into one's psyche. Most doctors aren't cross trained. You don't go to the vet, have them spay or neuter your dog, then ask them if your own tooth has a cavity...well I know one person that might, but she's the exception.
One in three is a pretty significant number. That is what surprises me. How can 33% of us be ignored and forgotten about? If I handed you and ice cream cone and said it's $5 and there is a two in three chance it will taste delicious, but a one in three chance it will taste as bad as a rock concert restroom smells, you probably wouldn't do it. There is a 67% chance you will have fun on this roller coaster, but a 33% you will get seriously hurt or killed...are you going to wait in line?
Although, there is tons of research, when I went to the major cancer resources to find out what help there was out there, the websites had surprisingly little information. The research is out there. It all basically says the same thing, but no one really seems to know what to do with that knowledge. And in the mean time people are falling through the cracks. I haven't thought about harming myself, but the studies do have morbidity rates that are higher than people not going through it.
As in many things with cancer, we need to start educating each other, and passing along what helps us, and that its a normal feeling, and how to get help. We've always been good about warning about cancer insomnia, scanxiety, and chemo brain, but not this whether it truly is PTSD or whatever it is. Maybe it's because it happens after most of us have left our support groups or no longer get the longer talks with the oncologist and their team. But we have to make a change somewhere. We have to get the word out. We have to help each other. We have to do something.
Her words struck me as odd. I know people with PTSD, and some of them have a lot more to worry about than I do. After all I was basically disappointed that I have to keep going back to the doctor, that I'm still a cancer patient. That's all. Yes, there are certain triggers, certain things that cause memories to come flooding back, but that's just life. That happens with lots of things right? Every time I smell cow manure, I get flash backs to the county fair and start look for deep fried anything.
Later on that day, I just Googled "PTSD" and "cancer", thinking I would find a few anecdotes here, or casual observations there. What popped up on the page astounded me. Studies, LOTS of studies on the subject. And they all came to basically the same conclusion, it's not just in our heads...well it is, technically, I guess...but a lot of us are experiencing it.
There were tons of articles but the same results seemed to be popping up in every study. One out of every three of us experience this. It only shows up AFTER active treatment, usually when patients are in their monitoring stage. It can start as soon as 6 months after active treatment, but many experience it at about the three year mark. And the trigger to cause the onset of the effects doesn't necessarily have to be cancer related, but it brings back the cancer thoughts.
Before I go any further, I don't think I have "post traumatic stress disorder". As I mentioned, I know people that have PTSD, and I wouldn't even begin to compare my problem with theirs. However, I do have SOMETHING going on. And the research shows that clearly a lot more of us do too.
That's when I started getting a little angry. Further reading on the studies shows that very few oncologists even realize that this is going on.
For those that haven't been to an oncology monitoring appointment it goes like this, you sit in a sterile waiting room (literally, because chemo knocks out your immune system). You look at the pile of old hard candy (because chemo also dries out your mouth), trying to decide if you are desperate enough to get a piece. Then the phlebotomist calls you, puts you on the scale while you try to claim that your shoes weigh 50 pounds a piece, takes your vitals, and sucks out about 4 gallons of blood for various tests, spells, and incantations. Then, before they shuffle you off to wait in the oncologist office, they ask where you are on the pain scale, physically and mentally (you know that little scale of various emojis before they were emojis, ranging from happy face emoji to frowny crying face emoji). That's where it dawned on me when the breakdown was.
Going into my last oncology appointment, I was excited. I had my monitoring extended once, but had been told by everyone...except the oncologist, that this would probably be my last appointment ever. When asked where I was psychologically, I picked a "3" out of "10" ("10" being the most stressed). After I was told to continue monitoring I was absolutely devastated. Had anyone stopped me on the way out the door and asked me to give my number on that scale again, it would have been an "8" or a "9". This was the failure. This is where no one is paying attention. And I don't necessarily blame the oncologists. Like many of the studies discovered, oncologist are trained to fight cancer, not delve into one's psyche. Most doctors aren't cross trained. You don't go to the vet, have them spay or neuter your dog, then ask them if your own tooth has a cavity...well I know one person that might, but she's the exception.
One in three is a pretty significant number. That is what surprises me. How can 33% of us be ignored and forgotten about? If I handed you and ice cream cone and said it's $5 and there is a two in three chance it will taste delicious, but a one in three chance it will taste as bad as a rock concert restroom smells, you probably wouldn't do it. There is a 67% chance you will have fun on this roller coaster, but a 33% you will get seriously hurt or killed...are you going to wait in line?
Although, there is tons of research, when I went to the major cancer resources to find out what help there was out there, the websites had surprisingly little information. The research is out there. It all basically says the same thing, but no one really seems to know what to do with that knowledge. And in the mean time people are falling through the cracks. I haven't thought about harming myself, but the studies do have morbidity rates that are higher than people not going through it.
As in many things with cancer, we need to start educating each other, and passing along what helps us, and that its a normal feeling, and how to get help. We've always been good about warning about cancer insomnia, scanxiety, and chemo brain, but not this whether it truly is PTSD or whatever it is. Maybe it's because it happens after most of us have left our support groups or no longer get the longer talks with the oncologist and their team. But we have to make a change somewhere. We have to get the word out. We have to help each other. We have to do something.
PRS Guitars, the Cure for Cancer...
For anyone that doesn't know, right before I had gotten diagnosed with cancer, I had saved up to buy a new PRS guitar. I had sold various things and was finally ready to make my new purchase. When getting ready to go to the store, I saw two separate ads for people selling used PRS guitars and another brand I was wanting to try as well. I realized if I bought used instead of new, I could get TWO guitars instead of one. And we all know, two is twice as good as one. I bought a PRS and the other brand. Later when one of the other sellers finally got around to contacting me back and offered to sell me the other PRS. I was enjoying the one I had, and still had a little bit of money saved, so I bought it as well.
As luck would have it, my surgery limited the amount of weight I could lift. Those PRS guitars I bought were just under the weight limit and were how I passed much of the time recovering from surgery and chemo. I decided to sell some more stuff I wasn't using on ebay (like parachute pants and a disco ball) and get a nice PRS guitar after I got well. I didn't get the chance. For the first Christmas after Chemo, my whole family got together and bought me one. It was a gift I never expected to get and one of the first pics of my son were taken with him holding it. A few days after Christmas, I walked into the music store with what little money I had been saving for a nice PRS (not nearly enough) and there sat the guitar that I had originally been saving up for in the first place, marked down drastically because it literally fell off of the back of a truck and chipped some paint. Although, not nearly as nice as the one my family had just gotten me, I had just enough cash to cover it, and decided to make the PRS story come around full circle by buying the one that made me start the journey in the first place.
Two years ago, I had the opportunity to meet Paul Reed Smith and had gone over in my mind everything I was going to say and thank him for what was basically a coincidence, but it meant a lot to me. All I managed to get out when I met him was my first name and I got too emotional to carry on any further.
Now I would say this is all review to my regular blog readers, but I can't imagine that anyone would actually come back to my page twice, it's really not that good, so that is what you have missed in the past.
As I said on my last post, I was expecting to be done with oncology visits and therefore done with cancer in May. The nurses this past November told me it was customary to schedule something big to celebrate breaking free of the cancer stigma. Paul Reed Smith was opening up the doors to the factory in June, just a few weeks after I was to be released, so that is the trip I planned for. That is the trip that would bring everything full circle. I started my cancer journey with PRS guitars, I would end it with a tour of the factory...except that didn't happen. I didn't get released. I got sentenced to an unknown number of years of continued monitoring.
I rolled into Maryland and on the PRS campus with a bittersweet feeling. This was supposed to be a celebration of being free, instead it was a reminder that I am still going to oncology visits. I am still a cancer patient. I am still living under that threat that I am not free and clear.
Now here is the thing. Paul Reed Smith is an actual guy, not just some made up brand. He's just a guy that likes playing guitars and tried to make a great guitar at good price. He doesn't know any of this is going on. And all I really wanted to do was say "thank you". My wife came with me to a private event that was essentially for the PRS "fan club". Paul was being very cordial and walking around to everyone talking to them, signing autographs, answering questions. He was working the room and making his way over to us. My wife was wanting him to come over, but I knew I wasn't ready. It wasn't the man that was making me emotional, it was the whole process, the whole history. I have had those PRS guitars for only about two weeks longer than I have been dealing with cancer. The two are linked in my mind for eternity. I can't separate the two. One helped me survive the other. I feel silly because it's just a hunk of wood and a little bit of metal, but that's where I spent my time and worked through my problems.
As Paul got closer, I knew I couldn't say thanks this time either. When you have had cancer, there are just certain things that trigger you memories and take you back to that time. It could be a food, a phone call, a doctor's office whatever. For me the flashbacks sometimes take me back to PRS guitars and or back to the urologist office when a guy I have just met asks me to drop my pants and starts playing with my ball. Luckily that only happens in doctors' offices (or what I was led to believe was a doctor's office. Fool me once...) So as Paul got closer, and as my wife got more excited to tell him what I hadn't been able to, I just had everything flood back into my memory. The cancer, the chemo, the celebration that didn't happen, and the seemingly endless years of monitoring. I couldn't take it. I walked out. No explanation, I just walked around to the side of the factory where no one could see me. I squatted in the grass. I walked by the pond. I messaged a good friend. I did everything to try to distract me from what I was feeling. It didn't work as well as I wanted.
I had decided I just needed to go through the factory alone. My wife decided to get something signed by Paul for our son, since ultimately the PRS guitars will be his one day. Cell service was non-existent in the factory and as soon as I emerged, my wife called me and asked where I was. She had gotten the autograph for my son and told Paul that I wanted to say thanks. Paul had recently had cancer affect people in his life and told her he knew exactly what I was going through and started searching for me. She said she would bring me back to him.
She found me, and took me in the tent. Paul had a line of people seeking autographs and I didn't want to interrupt. All of a sudden, he looks up and sees my wife, whispers something to his assistant, and made a beeline for us. I tried to keep it together. All I needed to say was thanks, I knew I could do that much. That is when he put his arm around me, told me what the people in his life had been through, and I broke down as he shared his pain. I did manage to say thanks, but that was about it. But that is what I needed to do. I may have shown up for the wrong reason, but I still accomplished the original mission. A week later, I watched Paul put on a presentation at another show. I no longer had to say thanks. I didn't go up to meet him with everyone else. He knows my pain, I know his, and I finally got to say thanks. Now I just need to learn how to play guitar halfway decent before the oncologist kicks me loose and everything will be complete.
I had decided I just needed to go through the factory alone. My wife decided to get something signed by Paul for our son, since ultimately the PRS guitars will be his one day. Cell service was non-existent in the factory and as soon as I emerged, my wife called me and asked where I was. She had gotten the autograph for my son and told Paul that I wanted to say thanks. Paul had recently had cancer affect people in his life and told her he knew exactly what I was going through and started searching for me. She said she would bring me back to him.
She found me, and took me in the tent. Paul had a line of people seeking autographs and I didn't want to interrupt. All of a sudden, he looks up and sees my wife, whispers something to his assistant, and made a beeline for us. I tried to keep it together. All I needed to say was thanks, I knew I could do that much. That is when he put his arm around me, told me what the people in his life had been through, and I broke down as he shared his pain. I did manage to say thanks, but that was about it. But that is what I needed to do. I may have shown up for the wrong reason, but I still accomplished the original mission. A week later, I watched Paul put on a presentation at another show. I no longer had to say thanks. I didn't go up to meet him with everyone else. He knows my pain, I know his, and I finally got to say thanks. Now I just need to learn how to play guitar halfway decent before the oncologist kicks me loose and everything will be complete.
Saturday, July 19, 2014
Testicular Cancer Top 10....or I Am Not A Doctor, But You Are Still Going To Tell Me About Your Nuts...
In the breast cancer community, there are a lot of sources for finding information on how to do self exams, what treatment options are, and how to cope afterwards. And while there are certainly many sources of information and non profits for so called "men's cancers", we aren't as open about discussing them. It is ironic that the same ones that like to boast about being so well endowed that they make donkeys jealous are the same ones afraid to ask anyone how to do an exam. I am not real sure what the reason for the disparity between the sexes is. Maybe it's because breasts are right up front where you can see them and testicles are hidden, except in European bathing suits. Or maybe how the great masters would always view breasts as these perfectly formed pieces of art that they would spend days sculpting into marble, while at the same time, the artists would make a guys junk look like a wadded up piece of paper with some concrete slapped on it. At any rate, the public perception about the two are not the same.
After I went through my fight, and if you have read any of my posts you know that I have no shame in discussing what one experiences with testicular cancer, I cannot tell you how many times friends, colleagues, and random strangers have pulled me aside and asked, "How did you know?" I certainly don't mind answering that question. I can explain how I found mine and then I usually refer to a website like http://www.testicularcancersociety.org/testicular-self-exam.html to get a more clinical and better explained way to do exams. Then the feeling of dread comes over me, because I have been through this enough to know what is coming next. The person will then describe, in great wrinkly and hairy detail, why they are asking me that question. So far, they have always stopped short of actually showing me, and I would like to keep it that way. Let's face it, they are not a very attractive piece of anatomy. One of the few good things about having a nutectomy (orchiectomy, if you want to get technical), is there is one less of those ugly things that you have to look at in the shower, and bump into random stuff with...oh, and you can do your self exams in half the time.
So in the spirit of changing the stigma of testicular cancer and breaking the silence, I will post before and after pictures of my...OK, not really, but I will answer some of the questions here, that I normally get asked in a hushed voice in the corner of a crowded room, or outside around the corner out of ear shot of the smokers, or in late night phone calls with heavy breathing...OK, that person never actually says what they want, but always hangs up after I tell them to do a self exam.
1. How to do a self exam? There are several sources for how to do a self exam including the one from the Testicular Cancer Society I mentioned above. Some places even offer shower cards just like some breast cancer foundations do. There are two things to remember. First do exams consistently. You will notice something changing down there long before anyone else will. I don't care how often you go to the doctor or what odd pastimes you may have, you will still notice first if you do regular exams. And the earlier you catch it, the less it spreads to other parts of your body. Second, we all know about shrinkage, so the boys have to be warm to get a good exam. That is why it is generally suggested during a bath or shower, rather than right after taking the Polar Bear Plunge. After all, you want things loose to feel details, cancer starts small and grows, you don't want things cold and shriveled like trying to feel two acorns stuffed in a leather wallet.
2. What if I find something? It's probably nothing, but do you want to take that chance with your life? Go to a doctor to be sure. You would be amazed of the things that hang out with two nuts such as hydroceles, spermatoceles, cysts, drummers (sorry, musician joke), most of which don't hurt anything. In my case, harmless hydroceles were found, but the issue is they can mask cancer, so I was taught to do an illumination test, where basically shining a flashlight behind the boys GENERALLY causes the harmless stuff to glow and the bad things to be dark. However, let your doctor determine that for you. That is not always the case and if done wrong, you can have cancer growing for months without realizing it.
3. If it is cancer, will they take my ball(s)? Most likely yes. That is why you want to catch it early so you only lose one. But ultimately, what is the big deal? I assure you that in the almost four years since "rightie" was removed, no one has noticed. I get just as many compliments down there as I always have.
4. Will my testosterone levels drop with only one nut? Maybe, but probably only slightly. My doctor put it to me this way, if you lose one lung or donate a kidney it doesn't mean you are running on half power. Usually both don't work at full power anyway, so the remaining one just works a little harder than before. My testosterone numbers are well into the normal range.
5. Will my sperm count drop? See above. The fun part is with testosterone testing you give a blood sample, but with sperm count testing there is no needle but there are dirty magazines. Even if you drop in half, you will still more than likely have enough to get the job done or get you in trouble, however you view that situation. Just a word of caution, I don't think the girl downtown offering to check your sperm levels for $5 dollars has had any medical training whatsoever.
6. Will I be able to have kids? God I hope so, because I had one, so if you can't then someone has some explaining to do! Yes, either the natural way or with frozen guys.
7. What is the first thing I should do after being diagnosed? Ask all of your hot female friends if they want to say "goodbye". OK, obviously that is a joke and probably wouldn't even work. But I would call an organization like livestrong.org especially if you are interested in having kids. They can tell you about certain grants that will pay for collection and storage of frozen guys, but the catch on some of them is you have to apply BEFORE you go to get the collection done.
8. Can the cancer come back? Yes it could, but that is why you talk to an oncologist to see what your options are. I opted for chemo for the peace of mind of not having to worry as much about it returning. A few weeks of feeling sick was more attractive to me than a lifetime of worry.
9. Do they just slice open the bag and take out the groceries? No! They go in from around your waist so they can take all of the plumbing too, just in case it has started spreading. So you can show people your scar without being obscene...unless you want to.
10. Do you miss it or have any phantom pain like an amputee would? No, and the good thing is, say hypothetically, you have a two and a half year old that runs at you full speed with a plastic Mike the Knight sword, the chances that he will hit your tender spot have now been cut in half (although he still manages to get me on the tender side EVERY SINGLE TIME! I am throwing that damn sword in the trash!).
So there you have it. The top ten (legitimate) questions I get asked in whispers and darkened corners. If you have anymore (legitimate) questions I will answer them like I did here, based on my own experiences or direct you to a trusted source. I am in no way a doctor, and I in no way want to see pictures, diagrams, or even very accurate descriptions.
After I went through my fight, and if you have read any of my posts you know that I have no shame in discussing what one experiences with testicular cancer, I cannot tell you how many times friends, colleagues, and random strangers have pulled me aside and asked, "How did you know?" I certainly don't mind answering that question. I can explain how I found mine and then I usually refer to a website like http://www.testicularcancersociety.org/testicular-self-exam.html to get a more clinical and better explained way to do exams. Then the feeling of dread comes over me, because I have been through this enough to know what is coming next. The person will then describe, in great wrinkly and hairy detail, why they are asking me that question. So far, they have always stopped short of actually showing me, and I would like to keep it that way. Let's face it, they are not a very attractive piece of anatomy. One of the few good things about having a nutectomy (orchiectomy, if you want to get technical), is there is one less of those ugly things that you have to look at in the shower, and bump into random stuff with...oh, and you can do your self exams in half the time.
So in the spirit of changing the stigma of testicular cancer and breaking the silence, I will post before and after pictures of my...OK, not really, but I will answer some of the questions here, that I normally get asked in a hushed voice in the corner of a crowded room, or outside around the corner out of ear shot of the smokers, or in late night phone calls with heavy breathing...OK, that person never actually says what they want, but always hangs up after I tell them to do a self exam.
1. How to do a self exam? There are several sources for how to do a self exam including the one from the Testicular Cancer Society I mentioned above. Some places even offer shower cards just like some breast cancer foundations do. There are two things to remember. First do exams consistently. You will notice something changing down there long before anyone else will. I don't care how often you go to the doctor or what odd pastimes you may have, you will still notice first if you do regular exams. And the earlier you catch it, the less it spreads to other parts of your body. Second, we all know about shrinkage, so the boys have to be warm to get a good exam. That is why it is generally suggested during a bath or shower, rather than right after taking the Polar Bear Plunge. After all, you want things loose to feel details, cancer starts small and grows, you don't want things cold and shriveled like trying to feel two acorns stuffed in a leather wallet.
2. What if I find something? It's probably nothing, but do you want to take that chance with your life? Go to a doctor to be sure. You would be amazed of the things that hang out with two nuts such as hydroceles, spermatoceles, cysts, drummers (sorry, musician joke), most of which don't hurt anything. In my case, harmless hydroceles were found, but the issue is they can mask cancer, so I was taught to do an illumination test, where basically shining a flashlight behind the boys GENERALLY causes the harmless stuff to glow and the bad things to be dark. However, let your doctor determine that for you. That is not always the case and if done wrong, you can have cancer growing for months without realizing it.
3. If it is cancer, will they take my ball(s)? Most likely yes. That is why you want to catch it early so you only lose one. But ultimately, what is the big deal? I assure you that in the almost four years since "rightie" was removed, no one has noticed. I get just as many compliments down there as I always have.
4. Will my testosterone levels drop with only one nut? Maybe, but probably only slightly. My doctor put it to me this way, if you lose one lung or donate a kidney it doesn't mean you are running on half power. Usually both don't work at full power anyway, so the remaining one just works a little harder than before. My testosterone numbers are well into the normal range.
5. Will my sperm count drop? See above. The fun part is with testosterone testing you give a blood sample, but with sperm count testing there is no needle but there are dirty magazines. Even if you drop in half, you will still more than likely have enough to get the job done or get you in trouble, however you view that situation. Just a word of caution, I don't think the girl downtown offering to check your sperm levels for $5 dollars has had any medical training whatsoever.
6. Will I be able to have kids? God I hope so, because I had one, so if you can't then someone has some explaining to do! Yes, either the natural way or with frozen guys.
7. What is the first thing I should do after being diagnosed? Ask all of your hot female friends if they want to say "goodbye". OK, obviously that is a joke and probably wouldn't even work. But I would call an organization like livestrong.org especially if you are interested in having kids. They can tell you about certain grants that will pay for collection and storage of frozen guys, but the catch on some of them is you have to apply BEFORE you go to get the collection done.
8. Can the cancer come back? Yes it could, but that is why you talk to an oncologist to see what your options are. I opted for chemo for the peace of mind of not having to worry as much about it returning. A few weeks of feeling sick was more attractive to me than a lifetime of worry.
9. Do they just slice open the bag and take out the groceries? No! They go in from around your waist so they can take all of the plumbing too, just in case it has started spreading. So you can show people your scar without being obscene...unless you want to.
10. Do you miss it or have any phantom pain like an amputee would? No, and the good thing is, say hypothetically, you have a two and a half year old that runs at you full speed with a plastic Mike the Knight sword, the chances that he will hit your tender spot have now been cut in half (although he still manages to get me on the tender side EVERY SINGLE TIME! I am throwing that damn sword in the trash!).
So there you have it. The top ten (legitimate) questions I get asked in whispers and darkened corners. If you have anymore (legitimate) questions I will answer them like I did here, based on my own experiences or direct you to a trusted source. I am in no way a doctor, and I in no way want to see pictures, diagrams, or even very accurate descriptions.
Saturday, July 5, 2014
Old Feelings Die Hard
Four years ago this week, I first noticed my lump. My wife had went on vacation with her mother and I stayed home alone to take care of work projects and watch the dogs. The past three years, I never really paid any attention to this date. After all, it's the date I just noticed something. It wasn't the date I was diagnosed. It wasn't the date I had my surgery or went through chemo or anything. But that is the weird thing about cancer, it seems you are never really completely free.
This year we had planned to take my two year old to my parents to watch fireworks for the 4th of July. From their house, they can see most of the fireworks. And we thought if we take him there, and he doesn't like the loud noises, or the bright lights, or he just starts being...well, a two year old, we could just take him in the house and not have to deal with traffic or crowds or that one guy that has to describe every firework loudly. After we had made these plans, my job made other plans, and my wife offered to take my son without me. It was a plan that was seemingly perfect, my son could experience the fireworks for the first time and I could keep skittish dogs company in the country.
That is when it hit me last night. I have been passing my scans without any problem, and my scanxiety has dropped to almost nothing. I only have to go to the oncologist twice a year now Even my dermatologist told me that she could tell I was really making a good effort to avoid skin cancer. So I haven't been thinking about cancer much at all. But last night was different. I was back to that place four years ago, just me and the dogs. The weird thing is, I didn't feel a lump, but I did have that feeling, a feeling I can't explain.
Most of us when we are diagnosed, aside from the shock of the "C" word, you get this "icky" feeling that something is growing inside of you that wants to kill you. The surgery can't come quick enough, you just want that stuff out today. That is the feeling I had last night. The feeling that I was all alone again. The feeling that something icky was going on. What made last night even freakier, was without thinking, I picked up that PRS guitar I bought four years ago today to play with while they were gone. It's not one I normally play, but it's what I grabbed last night. The only one that was light enough for me to play after my surgery. The one that got me through cancer. Just as my mind flashbacked to the bad time four years ago, I also subconsciously reached for the one thing that helped me get through it too.
As I approach what I consider my fourth cancerversary, I have been thinking about when I am done. Is it five years? Is it ten? Is it when you quit going to the oncologist...I hope it's not that one, because I think he has been saying "just a few more years" since my second visit. As far as my health is concerned, I think I am done. I have been getting clean scans. I have finally been dropping the weight I gained while I was sick. And for the most part, I feel better than before any of this happened. But I guess it's harder to gauge the feeling that we are done mentally being affected by cancer. Because last night, I sat alone and scared and realized I wasn't as done as I thought I was. Or maybe I am, because I grabbed that PRS, just like I did after my surgery, and played until I didn't have cancer anymore.
This year we had planned to take my two year old to my parents to watch fireworks for the 4th of July. From their house, they can see most of the fireworks. And we thought if we take him there, and he doesn't like the loud noises, or the bright lights, or he just starts being...well, a two year old, we could just take him in the house and not have to deal with traffic or crowds or that one guy that has to describe every firework loudly. After we had made these plans, my job made other plans, and my wife offered to take my son without me. It was a plan that was seemingly perfect, my son could experience the fireworks for the first time and I could keep skittish dogs company in the country.
That is when it hit me last night. I have been passing my scans without any problem, and my scanxiety has dropped to almost nothing. I only have to go to the oncologist twice a year now Even my dermatologist told me that she could tell I was really making a good effort to avoid skin cancer. So I haven't been thinking about cancer much at all. But last night was different. I was back to that place four years ago, just me and the dogs. The weird thing is, I didn't feel a lump, but I did have that feeling, a feeling I can't explain.
Most of us when we are diagnosed, aside from the shock of the "C" word, you get this "icky" feeling that something is growing inside of you that wants to kill you. The surgery can't come quick enough, you just want that stuff out today. That is the feeling I had last night. The feeling that I was all alone again. The feeling that something icky was going on. What made last night even freakier, was without thinking, I picked up that PRS guitar I bought four years ago today to play with while they were gone. It's not one I normally play, but it's what I grabbed last night. The only one that was light enough for me to play after my surgery. The one that got me through cancer. Just as my mind flashbacked to the bad time four years ago, I also subconsciously reached for the one thing that helped me get through it too.
As I approach what I consider my fourth cancerversary, I have been thinking about when I am done. Is it five years? Is it ten? Is it when you quit going to the oncologist...I hope it's not that one, because I think he has been saying "just a few more years" since my second visit. As far as my health is concerned, I think I am done. I have been getting clean scans. I have finally been dropping the weight I gained while I was sick. And for the most part, I feel better than before any of this happened. But I guess it's harder to gauge the feeling that we are done mentally being affected by cancer. Because last night, I sat alone and scared and realized I wasn't as done as I thought I was. Or maybe I am, because I grabbed that PRS, just like I did after my surgery, and played until I didn't have cancer anymore.
Saturday, October 26, 2013
Cancer Flashbacks With Paul Reed Smith
I am well aware that it has been a while since I last posted on here. I do have a reason. Trying to type with a toddler in the house means most of your writing looks like this "aklsjoun saiolkjdfslak klafjl;a". And even if he were not "helping" me on the keyboard, it is hard to concentrate on writing when you have a two foot tall individual that moves just shy of the speed of light, that you are yelling things at like "get your fingers out of the dogs' eyes", "no, the remote control doesn't belong in the toilet", "we can't blow bubbles outside right now, it's 14' outside, and dark", "get your fingers out of the dogs' eyes", "where did you find that, get it out of your mouth", "get your fingers out of the dogs' eyes", "no, the table lamp is not a toy", and "get your fingers out of the dogs' eyes". (In case you were wondering, learning the parts of the face was a very challenging time for our dogs' vision. Maybe we will have to find them a "seeing eye person".)
So, because of the delay, I am writing about an incident that happened in June. I think we have all been in a situation where a sound, or picture, or smell has brought you back to something in your past. For instance, every time I smell VapoRub, I think back to that time as a little child that my great grandmother rubbed it into an open wound. It still brings tears to my eyes. Well, for the most part I feel I am over this cancer stuff. Sure, I still have a few more years of CTscans, X-rays, blood tests, and all of the other monitoring. I am not exactly sure how many years, because asking an oncologist how much longer you need to see him, is similar to asking your parents on a road trip "are we there yet?". I think the answer has always been "4 or 5 more years" (for the oncologist visits, not the road trip...it just seemed like it took 4 or 5 years sometimes). Other than the endless doctors' appointments, I really don't have much to do with cancer. Oh there is still the solemn tone from friends you don't see very often asking "How are you doing?" But for the most part, I am living my life.
I love playing guitar. I play like I play golf, I don't play particularly well, but I don't take it too seriously and I enjoy doing it. When I had my surgery, I was restricted in what I could lift. Luckily, just before I was diagnosed, I had found some cheap used Paul Reed Smith guitars. They were the lightest guitars I owned, and were pretty much the only ones I could lift and play for a long time. They were the one thing that was able to get my mind off how bad things were for an hour or so at a time. When I finished my chemo, my family all pitched in and bought me a nice Paul Reed Smith for Christmas. The guitar means a lot to me for so many reasons. First I just like the guitar! But it symbolized closing the door on cancer. It meant a lot for my family to pitch in and get me something like that. And it was something I spent a lot of time with during my "chemo brain" months. So, a coincidental introduction to PRS guitars, ending up having a pretty significant impact on that period of my life.
Which brings me to what happened in June. Every year, Sweetwater Music has what basically amounts to "musician porn" at their campus in Fort Wayne, Indiana. Literally hundreds of manufacturers are there showing off all their new toys, letting you play with them, and they bring in dozens of endorsed artists (some more famous than others) to trick you into thinking that if you just had that equipment, you could make all those amazing sounds too! Well, Paul Reed Smith was on hand. Not just the company, Paul Reed Smith the actual person. In my past, I worked for a record company, regularly hanging out backstage and on tour buses of multi-platinum and even diamond selling artists (diamond is ten million copies). I was never nervous or star struck hanging out with rock stars, but being the geek I am, I was excited to see a guy that designs guitars.
One good thing is, I was right at home with my fellow geeks, because there was a full auditorium of us waiting to see him (although, I was one of the few that showed up an hour early to stand in line, and made it to the front row). I watched his presentation in awe when he talked about all the technical things that make his company's guitars sound so good. I had heard he was good about doing "meet and greets" with his fans, and throughout waiting in line, and his presentation, and...waiting in line again to meet him, I ran through my head exactly what I was going to say. I was going to tell him, how his products got me through some dark times. Thank him profusely. And maybe talk to him about the technical nuances of a quality guitar (not that I know what I am talking about, but I can fake it).
The problem with be one of the first ones in the auditorium for the presentation, is that means you are going to be one of the last ones out to stand in line for the meet and greet. The whole time in line, I ran over my little monologue in my head. Over and over again, as the line grew smaller and I moved closer and closer to this guy who really has no idea that his guitar helped me with my cancer fight (although his company does regular donate to cancer charities). Then the big moment, I am standing before THE Paul Reed Smith...and I feel like I am at the oncologist's office for the first time, all the emotion came flooding back from that day. I felt the fear, felt overwhelmed, I felt like I was going to burst into tears...but I WAS NOT going to do that...no matter what!
So, I stood before Paul Reed Smith, handed him part of my guitar to sign. And was afraid if I said anything I would have an emotional outburst. So, in an effort to hold back this flood of emotions, I stood there looking like I was probably about to punch him. He asked me if I would like the autograph personalized and my big speech that I had practiced over and over again, was now reduced to one word, "Tom". Yes, all that I had planned on saying, all that I wanted to thank him for was boiled down to me barely uttering my own name through clenched teeth. He politely signed my piece for me and I briskly walked out of there, trying not to break into an all out sprint as I headed to my car, hoping if I went fast enough I could outrun this emotional avalanche. But I was also hoping if I couldn't keep it together, I would be far enough away that no one would see me.
Now, let me just say one thing in my defense. The surgery I had to help prevent a different kind of cancer, has caused me to be a hypoglycemic. And sometimes when people have low blood sugar, they tend to get more intense emotions. And, because I am a big geek, I got so busy looking at musician porn, and standing in line an hour early, and sitting through a presentation, and standing in line again, that I went about 14 hours without eating (not a smart thing for a hypoglycemic to do). So I will blame part of this incident on that, so as not to appear to be such a wuss.
So, I didn't get to thank Paul Reed Smith. And to be honest, I don't know what he would have thought about it if I did. It's not like he found the lump, or performed the surgery, or administered the chemo, but he was still important to my recovery, even if that isn't why he got in the guitar business. But this incident says a lot about us cancer survivors. You never know what is going to help us get through a hard time. It could be a book, a phone call, visits from a friend, or a cheap used guitar. And it is hard to feel "done" with cancer when you are still going to doctors' appointments every few months. They tell you it's over with, but in the very next breath, tell you to come back in November. And just like any other major event in your life, you never know what trigger will bring you back a memory or a feeling, that you may or may not want to experience again. At least, I got to meet him. I got something signed to me personally. And I got something to eat so something like that didn't happen again.
Wednesday, March 27, 2013
When Are You Done With Cancer?
As I write this I am about two and a half years out of my cancer diagnosis and treatment. Aside from a little skin cancer scare (which turned out was nothing) one could say I have been done with cancer. However, that is not exactly how it works in the cancer game.
There are so many questions as to when you are officially no longer a cancer patient. Was it the surgery? The chemo? When you quit going to an oncologist? Or when you finally pay off all your medical bills? (In which case I will never be done.) In many ways I no longer feel like a cancer patient, but at the same time, at the beginning of every month I look at my calendar and see what doctors appointments I have this round. It is hard to feel "well" or "cured" when you are sitting in a waiting room all of the time. I mean who needs a People magazine subscription when you can read it for free every month while you wait for the nurse to call your name? The good news is the frequency of the appointments slowly grows further and further apart. I think I am down to CT scans once a year now (so I only have to drink a half gallon of nasty tasting water a year).
The funny thing is, because of the doctors' good reports you feel like your not well. Because of the type of work I do, I tend to run into people that I haven't seen for months or even a year and they always ask how I am doing With the frequency of doctors appointments my answer is usually,"Well, I was just at the doctor and they said I was fine." That is the Catch 22 of being in monitoring, you have to see an "ist" each month (oncologist, urologist, gastroenterologist, etc.) but at least they say you are doing good each time. You don't feel like you can say "Oh, the cancer thing is over." because you are still seeing an oncologist, but at the same time you don't feel like a real cancer patient because you are not having to go through any treatment.
On one hand, it is nice to have the peace of mind every month that you are safe for four more weeks. On the other hand things get so routine, you wonder why you are paying more and more for something you could probably do yourself at this point. Heck, I am in and out of my urologist's office so fast, I could probably just drive by his office slowly with my scrotum hanging out the car window and toss out my co-pay.
I think the biggest part of not feeling "over" cancer is the mental aspect of it. Every bump, twitch, even feeling tired when you don't think you should makes you wonder if just maybe it's something bigger. And not even your thoughts are safe. My one-year-old had been going through a phase where he wants me to hug me, or have me hold him, or just lean against me. Most people would just understand it is the clingy phase that all toddlers go through, but my mind wondered if he wasn't sensing something, that maybe I wouldn't be around much longer and he needed to get his quality time in while I was still alive.
Even happy dreams aren't safe. I know two people that have flatlined on operating tables and come back to life. They both tell of people that have died greeting them at the end of the tunnel and telling them that it's not their time yet to go back to earth. I have had some friends die and some family members die, but only one person in my life has died that I saw everyday, and would spend an hour just talking to everyday about whatever. Well, that person was in my dream the other night. He welcomed me into Heaven, showed me around, and we picked up on conversations we started before he died. I woke up feeling so good knowing that if I died, this person would be the one that brought me through the tunnel and took me to see my other friends and family that have already passed. But that good feeling quickly turned to dread, as I wondered why I was dreaming about dying and does my body know something that it hasn't shared with my brain yet. Maybe part of my brain does know and it is just not sharing the information with the rest of my brain the same way it does when I ask it where I put the car keys.
The biggest joy I have in life is watching my son play, which we weren't even sure we were going to be able to have when all this started. Even while sitting there just watching him run around like a drunk kamikaze gymnast, I worry about recurrence and not being around to watch him grow up. Or not being around and maybe his only memory of me will be me yelling at him to quit splashing in the dogs' water dish (which to be fair is something I do approximately 1500 times everyday).
So am I done with cancer? The doctors say "yes" but then tell me to schedule an appointment to come back and make sure it's still "yes". Physically, outside of underwear not fitting quite the way it used to, I feel like I am done with cancer. Mentally, the chemo fog has cleared up, but there is always that cancer cloud hanging over me, just like a summertime meteorologist's permanent "30% chance of storms". The ironic thing is the more my son shines the more I worried I get about that cancer cloud. But until then I will enjoy every second I get to spend with my son, even the hours on end I spend pulling him out of the dog dish, and hopefully live long enough to teach him how to check for testicular cancer on himself one day.
There are so many questions as to when you are officially no longer a cancer patient. Was it the surgery? The chemo? When you quit going to an oncologist? Or when you finally pay off all your medical bills? (In which case I will never be done.) In many ways I no longer feel like a cancer patient, but at the same time, at the beginning of every month I look at my calendar and see what doctors appointments I have this round. It is hard to feel "well" or "cured" when you are sitting in a waiting room all of the time. I mean who needs a People magazine subscription when you can read it for free every month while you wait for the nurse to call your name? The good news is the frequency of the appointments slowly grows further and further apart. I think I am down to CT scans once a year now (so I only have to drink a half gallon of nasty tasting water a year).
The funny thing is, because of the doctors' good reports you feel like your not well. Because of the type of work I do, I tend to run into people that I haven't seen for months or even a year and they always ask how I am doing With the frequency of doctors appointments my answer is usually,"Well, I was just at the doctor and they said I was fine." That is the Catch 22 of being in monitoring, you have to see an "ist" each month (oncologist, urologist, gastroenterologist, etc.) but at least they say you are doing good each time. You don't feel like you can say "Oh, the cancer thing is over." because you are still seeing an oncologist, but at the same time you don't feel like a real cancer patient because you are not having to go through any treatment.
On one hand, it is nice to have the peace of mind every month that you are safe for four more weeks. On the other hand things get so routine, you wonder why you are paying more and more for something you could probably do yourself at this point. Heck, I am in and out of my urologist's office so fast, I could probably just drive by his office slowly with my scrotum hanging out the car window and toss out my co-pay.
I think the biggest part of not feeling "over" cancer is the mental aspect of it. Every bump, twitch, even feeling tired when you don't think you should makes you wonder if just maybe it's something bigger. And not even your thoughts are safe. My one-year-old had been going through a phase where he wants me to hug me, or have me hold him, or just lean against me. Most people would just understand it is the clingy phase that all toddlers go through, but my mind wondered if he wasn't sensing something, that maybe I wouldn't be around much longer and he needed to get his quality time in while I was still alive.
Even happy dreams aren't safe. I know two people that have flatlined on operating tables and come back to life. They both tell of people that have died greeting them at the end of the tunnel and telling them that it's not their time yet to go back to earth. I have had some friends die and some family members die, but only one person in my life has died that I saw everyday, and would spend an hour just talking to everyday about whatever. Well, that person was in my dream the other night. He welcomed me into Heaven, showed me around, and we picked up on conversations we started before he died. I woke up feeling so good knowing that if I died, this person would be the one that brought me through the tunnel and took me to see my other friends and family that have already passed. But that good feeling quickly turned to dread, as I wondered why I was dreaming about dying and does my body know something that it hasn't shared with my brain yet. Maybe part of my brain does know and it is just not sharing the information with the rest of my brain the same way it does when I ask it where I put the car keys.
The biggest joy I have in life is watching my son play, which we weren't even sure we were going to be able to have when all this started. Even while sitting there just watching him run around like a drunk kamikaze gymnast, I worry about recurrence and not being around to watch him grow up. Or not being around and maybe his only memory of me will be me yelling at him to quit splashing in the dogs' water dish (which to be fair is something I do approximately 1500 times everyday).
So am I done with cancer? The doctors say "yes" but then tell me to schedule an appointment to come back and make sure it's still "yes". Physically, outside of underwear not fitting quite the way it used to, I feel like I am done with cancer. Mentally, the chemo fog has cleared up, but there is always that cancer cloud hanging over me, just like a summertime meteorologist's permanent "30% chance of storms". The ironic thing is the more my son shines the more I worried I get about that cancer cloud. But until then I will enjoy every second I get to spend with my son, even the hours on end I spend pulling him out of the dog dish, and hopefully live long enough to teach him how to check for testicular cancer on himself one day.
Friday, June 22, 2012
The Best Gift I Have Received Throws Up On Me...
When you are about to have your first child there are tons of tidbits of wisdom that people will tell you. I gladly listened to everything people told me making mental notes along the way. Having just made it six months with my new best friend, I feel I am becoming quite accustomed to this new life. Some of the things people told us were about the negative aspects of having a child. I think the big factor in this for us, is how badly we had wanted a child, how long we had been trying, and finally after the cancer/miscarriage/fertility treatments how much we went through before we were successful.
One thing we heard over and over again was how exhausted we would be. Now, I will admit we aren't as well rested as we were six months ago. I can't remember the last time we were able to just sleep in as long as we liked. But I certainly wouldn't call it "exhausted". One thing we have going for us, is our child has been an overnight sleeper since we brought him home from the hospital. I think the shortest he ever slept overnight was maybe four hours when he was first brought home. The other reason I don't think I am tired is I enjoy the time I get to spend with him. Think of something you really enjoyed, like for me going to Walt Disney World, for you it might be reading my blog...if it is something you really had fun doing, you get whatever sleep you can and do it again first chance you get.
The other very cliched comment is that you will never know how much love you will have for the baby. Waiting until forty-one to have my first child, trust me a lot of anticipation and love had built up. I love my little guy a lot, and that love started the day my wife walked out of the bathroom with a pee-soaked stick. What has surprised me is just how much I like being around him. Even from the beginning when all he was doing was laying there and messing diapers, I cherished every second with him. Now I will say this. He seems like a very happy baby and everyone tells us he is a happy baby. That certainly helps. Even when changing a diaper he looks up and smiles and either grabs my arm or if I am careless enough he will grab the clean diaper and play keep away with me, which is apparently very funny when you are six months old.
But then again everything seems to be funny to our six month old. A hand full of someone else's hair is freakin' hilarious! Rubbing bare feet on daddy's head or whiskers is also a great source of amusement. The phrase "peas and apples" is the greatest joke ever told, ranking right up there with "The Aristocrats". I have no idea why "peas and apples" induces uncontrollable laughter, but I think it's pretty obvious that he has his daddy's sophisticated sense of humor.
The other side is, I am probably one of those obsessive and over-protective parents. When you have gone through your own health scare you realize just how precious and fragile life is. Someone told us the other day that kids aren't that fragile at all, all three of theirs rolled off the bed at one point as babies. That led to a conversation after we left that person about how after the first roll off (or at the very least the second roll off) wouldn't you take precautions to prevent future roll offs? This person claimed there was no harm done...but there's one we think the jury is still out on.
I may have given my son his first real electric guitar this week as well (which means I did give him his first electric guitar). Now I know what you are thinking, "He's six months old, he can't play an electric guitar" and you are exactly right, that is why his is half the size of a normal one. And since it is difficult for him to strum and hold down the strings, I even brought out a thing that automatically moves the strings for him, so he can just focus on the fretboard for now. See, doesn't sound near as crazy now, does it?
What I am getting at, is this is the greatest gift I have ever been given. We waited a long time for him and went through a lot to get him. Even when during a diaper change he accidentally peed in his face, which literally scared the crap out of him, all I could do was clean him up and laugh. Being spit up on twice a day, doesn't bother me, I just add the clothes to the huge pile of other garments he finds creative ways to soil. In other words, even the bad times are some of the best times of my life, so you can imagine how great the good times are. And hopefully by next week we will be playing our guitars together...
One thing we heard over and over again was how exhausted we would be. Now, I will admit we aren't as well rested as we were six months ago. I can't remember the last time we were able to just sleep in as long as we liked. But I certainly wouldn't call it "exhausted". One thing we have going for us, is our child has been an overnight sleeper since we brought him home from the hospital. I think the shortest he ever slept overnight was maybe four hours when he was first brought home. The other reason I don't think I am tired is I enjoy the time I get to spend with him. Think of something you really enjoyed, like for me going to Walt Disney World, for you it might be reading my blog...if it is something you really had fun doing, you get whatever sleep you can and do it again first chance you get.
The other very cliched comment is that you will never know how much love you will have for the baby. Waiting until forty-one to have my first child, trust me a lot of anticipation and love had built up. I love my little guy a lot, and that love started the day my wife walked out of the bathroom with a pee-soaked stick. What has surprised me is just how much I like being around him. Even from the beginning when all he was doing was laying there and messing diapers, I cherished every second with him. Now I will say this. He seems like a very happy baby and everyone tells us he is a happy baby. That certainly helps. Even when changing a diaper he looks up and smiles and either grabs my arm or if I am careless enough he will grab the clean diaper and play keep away with me, which is apparently very funny when you are six months old.
But then again everything seems to be funny to our six month old. A hand full of someone else's hair is freakin' hilarious! Rubbing bare feet on daddy's head or whiskers is also a great source of amusement. The phrase "peas and apples" is the greatest joke ever told, ranking right up there with "The Aristocrats". I have no idea why "peas and apples" induces uncontrollable laughter, but I think it's pretty obvious that he has his daddy's sophisticated sense of humor.
The other side is, I am probably one of those obsessive and over-protective parents. When you have gone through your own health scare you realize just how precious and fragile life is. Someone told us the other day that kids aren't that fragile at all, all three of theirs rolled off the bed at one point as babies. That led to a conversation after we left that person about how after the first roll off (or at the very least the second roll off) wouldn't you take precautions to prevent future roll offs? This person claimed there was no harm done...but there's one we think the jury is still out on.
I may have given my son his first real electric guitar this week as well (which means I did give him his first electric guitar). Now I know what you are thinking, "He's six months old, he can't play an electric guitar" and you are exactly right, that is why his is half the size of a normal one. And since it is difficult for him to strum and hold down the strings, I even brought out a thing that automatically moves the strings for him, so he can just focus on the fretboard for now. See, doesn't sound near as crazy now, does it?
What I am getting at, is this is the greatest gift I have ever been given. We waited a long time for him and went through a lot to get him. Even when during a diaper change he accidentally peed in his face, which literally scared the crap out of him, all I could do was clean him up and laugh. Being spit up on twice a day, doesn't bother me, I just add the clothes to the huge pile of other garments he finds creative ways to soil. In other words, even the bad times are some of the best times of my life, so you can imagine how great the good times are. And hopefully by next week we will be playing our guitars together...
Tuesday, March 20, 2012
(Creating) Life after Testicular Cancer.
I know I was supposed to write this last week, but by then end of today's post you will understand why I am not always able to post when I want. As I have mentioned in the past, I was laid off from work exactly two weeks when I was diagnosed with testicular cancer. Two life changing events that came back to back. What only my very closest friends know what there was actually a third event that happened right after that.
We had been wanting to start a family for a while, and were actively trying for around a year. A few days before I started chemo we found out that we were pregnant. It seemed like the typical feel good story, boy loses job, boy loses ball, but before he lost that nut boy and girl get pregnant. There was a whirlwind of emotions, it was something we desperately wanted, but the timing couldn't be worse. Chemo works by being a very nasty drug that is easily absorbed by anything that grows quickly in the human body, like cancer cells, hair, taste buds, and unfortunately babies. Because of this the first week I had to take tons of precautions around my wife making sure that she did not come into any contact with anything that may have the chemo in it. Even using the bathroom involved closing the lid, covering the lid with a heavy towel, and flushing the toilet twice. I never realized how long it takes a toilet to flush until I had to stand, weakened from chemo, waiting for it to finish flushing twice so I could remove the towel and go back to my normal routine.
After we went through all of this trouble, we lost the baby. It was very early in the pregnancy, and to say we were stressed during this time would be an understatement. What we found out after this was the staggering percentage of first time pregnancies that end in miscarriage, however that didn't make us feel any better. It was a third blow to us in less than two months. It was the ray of hope we had been focused on through chemo. Of course many things ran through my mind, like was it my fault for missing a chemo precaution and maybe I should have postponed my treatment.
The next few weeks were a mass of confusing information. Some people say to try again right away, others say wait. Some doctors say don't try so soon after chemo, others say it is fine the swimmers either die from the chemo or are not affected. My urologist said to just give up for at least six months, but my oncologist urged us to see a fertility specialist because we "needed something good in our lives". And he was right.
The first thing a fertility specialist tries to determine is which partner is causing the trouble. This makes tons of sense, I mean treat the person with the problem(s), right? So, my poor wife goes through a series of tests that look like the set of a alien abduction movie. I still have nightmares about some other the stainless steel contraptions I saw. I also had to go through a series of grueling tests that involved me going into a room, and being provided with dirty magazines, dirty movies, and a cup. It was horrible for me, mainly because I had already read all of the magazines when we "banked" some samples before my surgery.
So after my wife goes through her series of probings and shots, and I watch a few movies, we find out that...surprise surprise the problem looks like it is with the guy with the testicular cancer and chemo. Who would've guessed? The doc was very supportive and said with very little intervention, we could use my frozen stuff and probably be successful. No nasty chemicals, no danger of having "Plus 8" after our names or being chased by reality TV producers, for the most part things are pretty normal...except one.
This technique required me to give my wife a shot in her gluteus maximus the night before the procedure. Our doctor was very supportive and involved so they even drew and "X" on the targeted butt cheek to show the exact spot that the injection needs to be placed. Well, the first round didn't work, so when went for the second try the next month, I asked the nurse if instead of an "X" if she could draw a happy face so I could "jab it between the eyes with the needle". See, these are the kinds of suggestions that would normally get you thrown out of your wife's doctor's appointments, but in our case the nurse drew the happy face. This seems all very funny at the doctor's office, but it results in uncontrolled giggling when you are sitting there with a giant needle getting reading to lance a happy face on your wife's posterior. For some reason, my bent over wife did not see the humor in the situation which only resulted in even more uncontrolled giggling from me. Luckily, we did not have to try it a third time because my wife said she was working on a few ideas of what she was going to have the nurse write on her butt to greet me the next round.
So, I will leave on this cliffhanger, did we get pregnant, did we have a baby, is the baby keeping me from blogging as regularly as I would like? I think you know the answer, but I will talk about it more tomorrow.
We had been wanting to start a family for a while, and were actively trying for around a year. A few days before I started chemo we found out that we were pregnant. It seemed like the typical feel good story, boy loses job, boy loses ball, but before he lost that nut boy and girl get pregnant. There was a whirlwind of emotions, it was something we desperately wanted, but the timing couldn't be worse. Chemo works by being a very nasty drug that is easily absorbed by anything that grows quickly in the human body, like cancer cells, hair, taste buds, and unfortunately babies. Because of this the first week I had to take tons of precautions around my wife making sure that she did not come into any contact with anything that may have the chemo in it. Even using the bathroom involved closing the lid, covering the lid with a heavy towel, and flushing the toilet twice. I never realized how long it takes a toilet to flush until I had to stand, weakened from chemo, waiting for it to finish flushing twice so I could remove the towel and go back to my normal routine.
After we went through all of this trouble, we lost the baby. It was very early in the pregnancy, and to say we were stressed during this time would be an understatement. What we found out after this was the staggering percentage of first time pregnancies that end in miscarriage, however that didn't make us feel any better. It was a third blow to us in less than two months. It was the ray of hope we had been focused on through chemo. Of course many things ran through my mind, like was it my fault for missing a chemo precaution and maybe I should have postponed my treatment.
The next few weeks were a mass of confusing information. Some people say to try again right away, others say wait. Some doctors say don't try so soon after chemo, others say it is fine the swimmers either die from the chemo or are not affected. My urologist said to just give up for at least six months, but my oncologist urged us to see a fertility specialist because we "needed something good in our lives". And he was right.
The first thing a fertility specialist tries to determine is which partner is causing the trouble. This makes tons of sense, I mean treat the person with the problem(s), right? So, my poor wife goes through a series of tests that look like the set of a alien abduction movie. I still have nightmares about some other the stainless steel contraptions I saw. I also had to go through a series of grueling tests that involved me going into a room, and being provided with dirty magazines, dirty movies, and a cup. It was horrible for me, mainly because I had already read all of the magazines when we "banked" some samples before my surgery.
So after my wife goes through her series of probings and shots, and I watch a few movies, we find out that...surprise surprise the problem looks like it is with the guy with the testicular cancer and chemo. Who would've guessed? The doc was very supportive and said with very little intervention, we could use my frozen stuff and probably be successful. No nasty chemicals, no danger of having "Plus 8" after our names or being chased by reality TV producers, for the most part things are pretty normal...except one.
This technique required me to give my wife a shot in her gluteus maximus the night before the procedure. Our doctor was very supportive and involved so they even drew and "X" on the targeted butt cheek to show the exact spot that the injection needs to be placed. Well, the first round didn't work, so when went for the second try the next month, I asked the nurse if instead of an "X" if she could draw a happy face so I could "jab it between the eyes with the needle". See, these are the kinds of suggestions that would normally get you thrown out of your wife's doctor's appointments, but in our case the nurse drew the happy face. This seems all very funny at the doctor's office, but it results in uncontrolled giggling when you are sitting there with a giant needle getting reading to lance a happy face on your wife's posterior. For some reason, my bent over wife did not see the humor in the situation which only resulted in even more uncontrolled giggling from me. Luckily, we did not have to try it a third time because my wife said she was working on a few ideas of what she was going to have the nurse write on her butt to greet me the next round.
So, I will leave on this cliffhanger, did we get pregnant, did we have a baby, is the baby keeping me from blogging as regularly as I would like? I think you know the answer, but I will talk about it more tomorrow.
Wednesday, July 6, 2011
Goodbye Ann Maree...
One of the first rules of joining the Wellness Community is that you are not supposed to mention what happened in the group outside the group. And I don't plan on breaking that rule today, just bending it a little. I am bending that rule, because Ann frequently talked about her experiences in her own blog and Ann's attitude helped me through my own cancer fight.
When you first join the Wellness Community, you go to an information meeting that tells you what to expect and what it's all about. There was only one other couple at our meeting and that was Ann and Al Maree. To look at the two of them, you couldn't guess which one was sick. Through some introductions, we learned Ann was the one in the battle with cancer. I am sure they told us more that night, but to be honest I didn't know what was going on in my own life at that time, much less those around me.
When I walked into my first regular group meeting, there sat Ann Maree. We went around the room introducing ourselves, our cancers, and our treatments. I heard this vibrant, energetic, and non-cancer looking person state that she has been battling Stage IV Breast Cancer for years. WHAT?!?! She didn't even look like she had a cold! This may sound odd, but that made me feel really good. No not that she had cancer, but that one can fight such a hard fight and not only survive, but live well while surviving. Suddenly I no longer felt like cancer was this dark tunnel I was struggling to walk through hoping to some day see the light at the end. Ann helped show me that cancer may be part of one's identity, but it doesn't have to be one's only identity.
Ann was fond of saying, "I have cancer, but cancer doesn't have me." She lived that motto to the end. It was her attitude that helped me to push myself when I felt I wasn't ready to be a normal person yet. Most of that pushing resulted in me hurting myself, but that is beside the point. Ann participated in more LiveStrong events than I probably ever will. Ann actually got out and rode her bike as many times as I look over at my dusty bike and think that I should probably get my fat butt on it.
Although I knew Ann was very sick (even though she never seemed to show it) and I knew she was getting sicker, I never thought this day would come. I hate to admit it, but I had slacked on reading her blog daily because once again, she seemed to be beating the odds and getting better. But then Saturday I got the news that she had passed through the network of current and former Wellness Community members. I was expecting an e-mail at anytime for Ann quoting Mark Twain "The report of my death was an exaggeration." All hope was lost when I saw that her husband Al was the one reporting Ann's passing.
I thank God that I met Ann (and Al). When I was thinking all cancer patients were gray, bald, anorexic-looking, hunched over, zombie-like things (and that I was about to become one), Ann showed me that people with a much harder fight than I can look...well...normal. And when I thought cancer would ruin my life, Ann showed me cancer only has as much control over you life as you let it. Hearing Ann's struggles and seeing her fight with such dignity and poise, I knew that with a little Faith I could make it through my much smaller battle.
This week there will be a "Celebration of Life" for Ann, which I am certain Ann gave Al detailed instructions on how it should be carried out. I believe in God and I believe in Heaven, and I certainly believe that no matter how nice life is on Earth, afterlife in Heaven is better, but still it is hard to see someone taken too soon go away. I don't like funerals, because often they don't focus on the gift of getting to know and experience the person in life, they seem to focus on missing them after they have passed on. Ann and Al obviously feel the same way and want to have that celebration of life, not a mourning of death. That being said, I haven't decided yet if I am going this week or not. I would love to go to the event and share what an inspiration both Al and Ann have been for me the past year, but I know ultimately there will be tears and sorrow as well. Conversely, when I last saw Ann (although she was getting sicker) she looked as vibrant and was defiant as ever and I kinda want to seal that as my last memory of her. Regardless of whether I go or not, I am sincerely thankful to God that I got to meet both Ann and Al, and I am a very sad that I will not see Ann again. My heart goes out to Al as he continues Ann's Journey without her.
When you first join the Wellness Community, you go to an information meeting that tells you what to expect and what it's all about. There was only one other couple at our meeting and that was Ann and Al Maree. To look at the two of them, you couldn't guess which one was sick. Through some introductions, we learned Ann was the one in the battle with cancer. I am sure they told us more that night, but to be honest I didn't know what was going on in my own life at that time, much less those around me.
When I walked into my first regular group meeting, there sat Ann Maree. We went around the room introducing ourselves, our cancers, and our treatments. I heard this vibrant, energetic, and non-cancer looking person state that she has been battling Stage IV Breast Cancer for years. WHAT?!?! She didn't even look like she had a cold! This may sound odd, but that made me feel really good. No not that she had cancer, but that one can fight such a hard fight and not only survive, but live well while surviving. Suddenly I no longer felt like cancer was this dark tunnel I was struggling to walk through hoping to some day see the light at the end. Ann helped show me that cancer may be part of one's identity, but it doesn't have to be one's only identity.
Ann was fond of saying, "I have cancer, but cancer doesn't have me." She lived that motto to the end. It was her attitude that helped me to push myself when I felt I wasn't ready to be a normal person yet. Most of that pushing resulted in me hurting myself, but that is beside the point. Ann participated in more LiveStrong events than I probably ever will. Ann actually got out and rode her bike as many times as I look over at my dusty bike and think that I should probably get my fat butt on it.
Although I knew Ann was very sick (even though she never seemed to show it) and I knew she was getting sicker, I never thought this day would come. I hate to admit it, but I had slacked on reading her blog daily because once again, she seemed to be beating the odds and getting better. But then Saturday I got the news that she had passed through the network of current and former Wellness Community members. I was expecting an e-mail at anytime for Ann quoting Mark Twain "The report of my death was an exaggeration." All hope was lost when I saw that her husband Al was the one reporting Ann's passing.
I thank God that I met Ann (and Al). When I was thinking all cancer patients were gray, bald, anorexic-looking, hunched over, zombie-like things (and that I was about to become one), Ann showed me that people with a much harder fight than I can look...well...normal. And when I thought cancer would ruin my life, Ann showed me cancer only has as much control over you life as you let it. Hearing Ann's struggles and seeing her fight with such dignity and poise, I knew that with a little Faith I could make it through my much smaller battle.
This week there will be a "Celebration of Life" for Ann, which I am certain Ann gave Al detailed instructions on how it should be carried out. I believe in God and I believe in Heaven, and I certainly believe that no matter how nice life is on Earth, afterlife in Heaven is better, but still it is hard to see someone taken too soon go away. I don't like funerals, because often they don't focus on the gift of getting to know and experience the person in life, they seem to focus on missing them after they have passed on. Ann and Al obviously feel the same way and want to have that celebration of life, not a mourning of death. That being said, I haven't decided yet if I am going this week or not. I would love to go to the event and share what an inspiration both Al and Ann have been for me the past year, but I know ultimately there will be tears and sorrow as well. Conversely, when I last saw Ann (although she was getting sicker) she looked as vibrant and was defiant as ever and I kinda want to seal that as my last memory of her. Regardless of whether I go or not, I am sincerely thankful to God that I got to meet both Ann and Al, and I am a very sad that I will not see Ann again. My heart goes out to Al as he continues Ann's Journey without her.
Monday, May 16, 2011
Cancer Made Me Fat And Apparently Fat People Sweat A Lot
OK, so I guess cancer didn't directly make me fat, but it certainly helped me pack on some pounds. Between the inactivity following my surgery, the inactivity following chemotherapy, and the fact that my chemo taste change didn't effect my love for all stuff fattening, I have gained weight.
I realized this has become a problem when my wife punched me in the middle of the night, ripped the blankets off my previously slumbering body and said, "You're sweating on the clean sheets." We do have other sheets, and I could even wash them every single day, but she thought all of these things through and decided assaulting a sleeping cancer patient was the best course of action.
While hurting myself mowing the lawn the other day, I noticed I seemed to be sweating more than I had in the past. I first attributed that to my high metabolism and my well toned body, then I realized I didn't have either one. And it seems just about anything can cause me to break a sweat anymore, cleaning around the house, working around outside, walking the dogs on a hot sunny day, walking the dogs on a cold rainy day, walking up the stairs to get a Little Debbie, eating a Little Debbie, thinking about eating Little Debbies, typing "Little Debbie", and apparently sleeping.
There seem to be another side effect to my recent weight gain as well, my hypoglycemia seems to be getting worse. This is a condition where my sugar will drop and I have to...well find something with sugar. They make glucose tablets designed to get the sugar back into your system quickly, and you would think something made to shoot up your sugar would be made at least remotely sweet tasting, but it really taste like compressed baby powder, except drier. This hasn't been a problem until I started getting more and more active lately. Apparently your sugar doesn't drop when you sit around all day ingesting sugar. Seeing some of the weird things people get disability payments for these days, I wonder if I can get the government to pay me to sit around all day ingesting sugary goodness...and maybe even pay for my sugary goodness as well.
But therein lies the irony in my whole situation. I want to get more fit and be more active, which causes me to hurt myself, which causes me to be less active. So, to make up for that, I try to eat healthier and avoid sugary stuff, which causes my sugar to nosedive, which forces me to eat more sugary stuff. You see my dilemma. I can't complain too much though, if the worst lingering effect of beating cancer is having to sit around on my rump eating Little Debbies and sweating. But if I didn't complain about something, I wouldn't have anything to write about today. So, here I am feeling a little better, but recovering a little slower. Luckily I don't have any pressing projects anytime soon that will require me to exert myself too much and we have a large stash of crappy food to keep my sugar levels up. I guess life ain't too bad after all.
I realized this has become a problem when my wife punched me in the middle of the night, ripped the blankets off my previously slumbering body and said, "You're sweating on the clean sheets." We do have other sheets, and I could even wash them every single day, but she thought all of these things through and decided assaulting a sleeping cancer patient was the best course of action.
While hurting myself mowing the lawn the other day, I noticed I seemed to be sweating more than I had in the past. I first attributed that to my high metabolism and my well toned body, then I realized I didn't have either one. And it seems just about anything can cause me to break a sweat anymore, cleaning around the house, working around outside, walking the dogs on a hot sunny day, walking the dogs on a cold rainy day, walking up the stairs to get a Little Debbie, eating a Little Debbie, thinking about eating Little Debbies, typing "Little Debbie", and apparently sleeping.
There seem to be another side effect to my recent weight gain as well, my hypoglycemia seems to be getting worse. This is a condition where my sugar will drop and I have to...well find something with sugar. They make glucose tablets designed to get the sugar back into your system quickly, and you would think something made to shoot up your sugar would be made at least remotely sweet tasting, but it really taste like compressed baby powder, except drier. This hasn't been a problem until I started getting more and more active lately. Apparently your sugar doesn't drop when you sit around all day ingesting sugar. Seeing some of the weird things people get disability payments for these days, I wonder if I can get the government to pay me to sit around all day ingesting sugary goodness...and maybe even pay for my sugary goodness as well.
But therein lies the irony in my whole situation. I want to get more fit and be more active, which causes me to hurt myself, which causes me to be less active. So, to make up for that, I try to eat healthier and avoid sugary stuff, which causes my sugar to nosedive, which forces me to eat more sugary stuff. You see my dilemma. I can't complain too much though, if the worst lingering effect of beating cancer is having to sit around on my rump eating Little Debbies and sweating. But if I didn't complain about something, I wouldn't have anything to write about today. So, here I am feeling a little better, but recovering a little slower. Luckily I don't have any pressing projects anytime soon that will require me to exert myself too much and we have a large stash of crappy food to keep my sugar levels up. I guess life ain't too bad after all.
Sunday, May 15, 2011
I Did, I Did, I Did Hurt Myself...
I sat around yesterday, glad that the rain that threatened off and on was around, it gave me a great excuse to avoid re-ripping my incision/mowing the ditch. Everything was going well until late afternoon, when I saw the sun poke out and illuminate the ditch in all its glorious overgrownedness. In a moment of extreme enthusiasm and lack of clarity, I decide to rush out, grab the push mower, and hurt myself.
The push mower has not been started since before my surgery, sometime in August. Of all the possible scenarios I ran in my mind on how to hurt myself, the one I forgot about was trying to start a push mower. I pulled the cord...and pulled the cord...and pulled the cord...pulled the cord...pulled the cord...pulled my incision...pulled the cord, with each pull I came a little closer to ripping my incision and the mower got no closer to starting. Even though I only have one testicle, I have enough testosterone to realize, if something doesn't work, you can always pour gas in it. Which is exactly what I did, and the mower started right up...in my workshop. But at least I knew that the mower starts. I loaded it up with the lawn tractor, and headed down to the ditch. I brought along my "whacking stick" which I use for chopping limbs (of trees...so far), hacking up rogue snakes (FYI, all snakes are rogue), and using for leverage/stability as I drop the mower off the side of the cliff we call a ditch. I don't know how to describe exactly what this tool is. It's about five feet long, and has a sharp hooked blade, which may have been an old way to harvest corn, or chase teenagers through fields while wearing a white William Shatner mask, or to run after Dr. Frankenstein's monster. Today it was also used as a cane.
I went to the top of the hill over looked the ditch and pulled the cord...pulled the cord...pulled the cord...pulled a muscle...pulled the cord. Luckily, I brought down a gas can with me so I used the whacking stick as a screwdriver to take off the breather and poured some more gas into the beast. The next pull, she roared to life. I was dreading pushing the mower over the edge, because that meant I had to pull it back up again. I slowly lowered it down, leaning heavily on the whacking stick, the mower started sputtering due to the extreme angle, and I started sputtering due to being fat and lazy for several months. Each pass, I struggled with lowering it down and pulling it up, while jamming the whacking stick in to the ground and using it to help pull the mower back up again. This was working fine, but I forgot one thing about living in the country, people (as in everyone that drives by) wave at you, and it's just not neighborly to not wave back. So in the midst of this delicate balancing act of using one hand to lower the mower down and the other hand death gripping the whacking stick, I have to pause to wave at every car that came by (because they waved at me) and apparently I-70 was shut down and rerouted on our road.
Eventually, I finished the hardest physical part, next I had to mow near the road. When mowing near the road, you not only have to look down for snakes to whack, but you have to be aware of traffic coming from the left and the right, and since we live at a "T" in the road, you also have to look out for traffic coming directly at your back. I know what you are thing, if I am mowing the ditch, why am I worried about traffic on the road? Well, several reasons, farm machinery is wider that your average car, so you have to be wary of it hanging over the side of the road, or cars avoiding oversized farm machinery and hanging over the side of the road, plus I frequently have to back into the road to mow this part, and I also have to mow around all the tire tracks IN OUR DITCH so obviously someone has managed to drive exactly where I am mowing before!
I have several theories as to why people drive in our ditch. Some just misjudge the curve and come around there way too fast. And this particular intersection is a one and a half way stop. There is one regular stop sign, and one "Stop Except When Turning Right" sign (which in every other state is just a "Yield") and the third way you don't have to stop no matter which way you're turning. This leads to confusion and thereby most people treat is as a What-Stop-Sign? intersection, leading to a lot of squealing and swerving around oncoming traffic. There also tend to be a lot of drunks that like to run into the ditch and sometimes for fun, ram the electricity pole. And finally I think a lot of people are just so busy looking for people to wave to that they don't pay attention to where they are going and run off the road.
So here I am, looking down for snakes to whack, looking left, looking right, looking behind me, looking up (because I don't want to be surprised by SEAL Team VI), pushing the mower with one arm, pulling on my whacking stick with the other arm, and waving at anything that moves. I was about three quarters done when I started to feel that familiar "tug" down below. No not my bowels, that was earlier, I am talking about my incision tugging to warn me that it doesn't like what I am doing and it threating to let loose. So, after getting this obvious warning sign, I did what all men would do and decided the best thing to do would be to stop, leave the rest and go in and take it easy. I did, I really did decide that would be the best thing, but I still kept mowing until I finished. It was about this time that my wife and mother-in-law came back from the cemetery, or store, or family Catholic event, or where ever they were and I saw them stop in the driveway way away from where I was mowing and wait to talk to me. Now it was pretty obvious that I was doing something, and it was also pretty obvious that whatever they had been doing previously, they were now sitting in an air conditioned car. Since they were waiting for me to stop what I was doing, walk from the edge of the yard to the driveway (which I estimate is a walk of approximately ten miles, or at least that's what it feels like when you have been mowing, waving, and keeping your insides from spilling out), I once again used my superior Man Reasoning Abilities and decide to ignore them and keep mowing. I finally finished the mowing and much like how a marathon winner will collapse as he/she crosses the finish line with tears of joy running down their face, I fell back on to the lawn tractor and let out a very manly man-whimper.
As soon as I stopped, I could tell that my incision wasn't doing well, and I had planned to just sit on the couch the rest of the night and hold my crotch, something that seemed to make even more sense now that I pulled my incision. Then my wife came down and asked if I would go with her to Wal-mart. For some reason I said "yes". I think I said "yes" because she said we were only going for two things, and I forgot in Wal-mart Speak, two things is actually forty-seven things that we will grab them by alternately criss-crossing the full length of the store approximately eighty-three times. I don't know how the math works out on that, I just know that's what happens.
So, for the rest of last night and all of today, I have been limping around holding my side, like that is actually helping at all, but since that is the only thing I can think to do, I keep doing it. The good news is that I didn't push myself to the "pop" just the tug. So I hope this will all be better soon. And if nothing else, I can use this for leverage next time someone wants me to mow the lawn.
The push mower has not been started since before my surgery, sometime in August. Of all the possible scenarios I ran in my mind on how to hurt myself, the one I forgot about was trying to start a push mower. I pulled the cord...and pulled the cord...and pulled the cord...pulled the cord...pulled the cord...pulled my incision...pulled the cord, with each pull I came a little closer to ripping my incision and the mower got no closer to starting. Even though I only have one testicle, I have enough testosterone to realize, if something doesn't work, you can always pour gas in it. Which is exactly what I did, and the mower started right up...in my workshop. But at least I knew that the mower starts. I loaded it up with the lawn tractor, and headed down to the ditch. I brought along my "whacking stick" which I use for chopping limbs (of trees...so far), hacking up rogue snakes (FYI, all snakes are rogue), and using for leverage/stability as I drop the mower off the side of the cliff we call a ditch. I don't know how to describe exactly what this tool is. It's about five feet long, and has a sharp hooked blade, which may have been an old way to harvest corn, or chase teenagers through fields while wearing a white William Shatner mask, or to run after Dr. Frankenstein's monster. Today it was also used as a cane.
I went to the top of the hill over looked the ditch and pulled the cord...pulled the cord...pulled the cord...pulled a muscle...pulled the cord. Luckily, I brought down a gas can with me so I used the whacking stick as a screwdriver to take off the breather and poured some more gas into the beast. The next pull, she roared to life. I was dreading pushing the mower over the edge, because that meant I had to pull it back up again. I slowly lowered it down, leaning heavily on the whacking stick, the mower started sputtering due to the extreme angle, and I started sputtering due to being fat and lazy for several months. Each pass, I struggled with lowering it down and pulling it up, while jamming the whacking stick in to the ground and using it to help pull the mower back up again. This was working fine, but I forgot one thing about living in the country, people (as in everyone that drives by) wave at you, and it's just not neighborly to not wave back. So in the midst of this delicate balancing act of using one hand to lower the mower down and the other hand death gripping the whacking stick, I have to pause to wave at every car that came by (because they waved at me) and apparently I-70 was shut down and rerouted on our road.
Eventually, I finished the hardest physical part, next I had to mow near the road. When mowing near the road, you not only have to look down for snakes to whack, but you have to be aware of traffic coming from the left and the right, and since we live at a "T" in the road, you also have to look out for traffic coming directly at your back. I know what you are thing, if I am mowing the ditch, why am I worried about traffic on the road? Well, several reasons, farm machinery is wider that your average car, so you have to be wary of it hanging over the side of the road, or cars avoiding oversized farm machinery and hanging over the side of the road, plus I frequently have to back into the road to mow this part, and I also have to mow around all the tire tracks IN OUR DITCH so obviously someone has managed to drive exactly where I am mowing before!
I have several theories as to why people drive in our ditch. Some just misjudge the curve and come around there way too fast. And this particular intersection is a one and a half way stop. There is one regular stop sign, and one "Stop Except When Turning Right" sign (which in every other state is just a "Yield") and the third way you don't have to stop no matter which way you're turning. This leads to confusion and thereby most people treat is as a What-Stop-Sign? intersection, leading to a lot of squealing and swerving around oncoming traffic. There also tend to be a lot of drunks that like to run into the ditch and sometimes for fun, ram the electricity pole. And finally I think a lot of people are just so busy looking for people to wave to that they don't pay attention to where they are going and run off the road.
So here I am, looking down for snakes to whack, looking left, looking right, looking behind me, looking up (because I don't want to be surprised by SEAL Team VI), pushing the mower with one arm, pulling on my whacking stick with the other arm, and waving at anything that moves. I was about three quarters done when I started to feel that familiar "tug" down below. No not my bowels, that was earlier, I am talking about my incision tugging to warn me that it doesn't like what I am doing and it threating to let loose. So, after getting this obvious warning sign, I did what all men would do and decided the best thing to do would be to stop, leave the rest and go in and take it easy. I did, I really did decide that would be the best thing, but I still kept mowing until I finished. It was about this time that my wife and mother-in-law came back from the cemetery, or store, or family Catholic event, or where ever they were and I saw them stop in the driveway way away from where I was mowing and wait to talk to me. Now it was pretty obvious that I was doing something, and it was also pretty obvious that whatever they had been doing previously, they were now sitting in an air conditioned car. Since they were waiting for me to stop what I was doing, walk from the edge of the yard to the driveway (which I estimate is a walk of approximately ten miles, or at least that's what it feels like when you have been mowing, waving, and keeping your insides from spilling out), I once again used my superior Man Reasoning Abilities and decide to ignore them and keep mowing. I finally finished the mowing and much like how a marathon winner will collapse as he/she crosses the finish line with tears of joy running down their face, I fell back on to the lawn tractor and let out a very manly man-whimper.
As soon as I stopped, I could tell that my incision wasn't doing well, and I had planned to just sit on the couch the rest of the night and hold my crotch, something that seemed to make even more sense now that I pulled my incision. Then my wife came down and asked if I would go with her to Wal-mart. For some reason I said "yes". I think I said "yes" because she said we were only going for two things, and I forgot in Wal-mart Speak, two things is actually forty-seven things that we will grab them by alternately criss-crossing the full length of the store approximately eighty-three times. I don't know how the math works out on that, I just know that's what happens.
So, for the rest of last night and all of today, I have been limping around holding my side, like that is actually helping at all, but since that is the only thing I can think to do, I keep doing it. The good news is that I didn't push myself to the "pop" just the tug. So I hope this will all be better soon. And if nothing else, I can use this for leverage next time someone wants me to mow the lawn.
Saturday, May 14, 2011
Summer's Here, Time To Hurt Yourself!
The past couple of days, I have had every intention of hurting myself. No not in one of those cries for help sort of ways, but just in pushing my self more and more to get back to normal. I still haven't tackled the dangling a push mower down the ditch yet. I am really afraid that may undo all the healing I have been doing, so when I do finally get around to attempting it, I will do it as gingerly as one can dangle a push mower down a ditch without simultaneously chopping off body parts. Just the fact that the engine starts to cut out because the mower is at such an extreme angle that it can't get gas, shows that maybe this isn't a recommended use of this particular mower.
However, that wasn't a problem yesterday. I had intended to do it, but secretly hoped something would come up to keep me from having to do it, and luckily plenty of things did. I spent some of the early part of the day helping my good friend with the project we are tackling. After that I waited for a HVAC company that claims "1 hour service" to call me back....that's been about 36 hours ago, and I am still waiting for a call back on the message I left. The reason, our thermostat decided that when the air conditioner kicks on, the house will cool down like it is supposed to, but the temperature reading will go UP! And that keeps the air conditioner on. You notice this when you look at the thermostat and it reads 87, while the other thermometer in the house reads 72 (and that is the real disparity in numbers we had when we first noticed the problem). A little research on the company turned up information that all electronic thermostats from this particular company do this. I won't mention their name because I don't want to embarrass Honeywell. I finally called in to our HVAC company through a different line (not a repair line) and asked them if they could fix this. They said yes they would replace it...in five days. I asked if they carried any other brands than the one they installed and they didn't. Frustrated I decided to runaway from the problem and went out to mow some of the muddy areas of the yard with the riding mower.
Now our mower is an commercial grade mower that we had to buy because someone keeps running into stuff bending the deck on regular mowers. I won't say who that someone is, but it's not me and it's probably my wife. Because of this, the mower weighs 1400 lbs. (about 650Kg) and because of its massive weight it gets stuck if there is any amount of moisture on the ground. While attempting to mow the parts of the yard that were too wet before, I hit a puddle or moss or gnat pee, whatever it was, the mower became hopelessly stuck. Now for reasons that I won't go into right now, I am the only one currently able to run this mower, so there was no one to drive the mower while I attempted to pull it out. So I did one any red blooded American male would do that has a Jeep and at least one ball (which I barely qualify for), I hooked up the Jeep and dropped it in four wheel drive low and jerked the crap out of it. You may have seen in the news where the day was .25 seconds shorter yesterday, that's because the massive torque of my Jeep pulling out this mower actually stopped the Earth's rotation for a brief moment. After these shenanigans were done, it was pretty much too late to attempt the ditch mowing/incision ripping yesterday.
So today I got up and went to a hardware store to find a thermostat that didn't have "Honeywell" stamped on it. I found one and then had to pick up a bag of concrete for another project we are doing. I found the correct type of concrete (for the record, there are approximately 75 different types of concrete and no matter what your project, there will be exactly 1 (one) bag that kinda fits what you are needing to do, and it will be on a very high shelf). I look straight at the bag...literally, because someone at Home Depot decided that this particular type of concrete needed to be about five feet in the air, and it dawned on me as I read "80 lbs." on the side of the bag that: A) I haven't lifted 80 lbs. since my surgery, I am officially supposed to be closer to 30lbs., and B) I can't bring the Jeep in to help me with this one. I briefly thought about asking for help, but two things occurred to me: 1) Guys are not supposed to ask for any sort of help whatsoever in a hardware store unless it is a veiled attempt to prove they know more than the person they are talking to, and 2) I have about as much chance of finding and employee at Home Depot to help me as I do of finding the Loch Ness Monster, Elvis, Jimmy Hoffa, and a regular cast member from Alf. Now Andrea Elson did walk by while I was contemplating the next move, but without Elvis, Jimmy, and Nessie she wouldn't have been much help. So I did what any self respecting guy would do, I picked up the bag anyway, rather than get help, and waited for the "pop" down below. I firmly grabbed the bag and just as gracefully has a Olympic weight lifter clean and jerks 1000 lbs., I put the concrete in the cart...OK, it was less like an Olympic weight lifter and more like a out of shape fat guy struggling to lift more weight than he lifted in eight months (outside of Golden Corral) all the while trying not drag the bag (which they for some reason make out of paper just slightly thicker than tissue paper) over anything that might snag it, causing it to burst open cartoonishly burying my feet in 80 lbs. of concrete, while at the same time trying to keep me from bursting open cartoonishly burying my feet in a large pile of my intestines. Unfortunately for the person watching me on the security camera I was able to load the concrete without any comic mishaps (yes, they actually have a sign in the concrete section pointing to the security camera, maybe that is a sign you are way understaffed if someone can grab an 80 lbs. bag of concrete and no one notices nor is able to catch someone fleeing with 80 lbs. of concrete).
Eventually, I made it home and the first thing I had to do, with the air conditioner running like an out of control Trane, was replace the thermostat. The thermostat contains slightly more wires than the Space Shuttle, except with fewer directions. After approximately 47 hours of cursing, reading, taking a Spanish course, reading the other manual, taking a Hindi course, calling tech support, and some Eeny Meeny Miney Mo, I was able to hook up the thermostat with a minimum amount of smoke and sparks. As I was wrapping up, a large storm hit, effectively ending my mowing/stomach shredding/toe slicing plans for the day.
I don't know if the events keeping me from mowing the ditch are a bit of Divine Intervention or just me being lazy and slow, but I will welcome the postponements no matter what the reasons. I just don't know what I am going to break to get out of it tomorrow...
However, that wasn't a problem yesterday. I had intended to do it, but secretly hoped something would come up to keep me from having to do it, and luckily plenty of things did. I spent some of the early part of the day helping my good friend with the project we are tackling. After that I waited for a HVAC company that claims "1 hour service" to call me back....that's been about 36 hours ago, and I am still waiting for a call back on the message I left. The reason, our thermostat decided that when the air conditioner kicks on, the house will cool down like it is supposed to, but the temperature reading will go UP! And that keeps the air conditioner on. You notice this when you look at the thermostat and it reads 87, while the other thermometer in the house reads 72 (and that is the real disparity in numbers we had when we first noticed the problem). A little research on the company turned up information that all electronic thermostats from this particular company do this. I won't mention their name because I don't want to embarrass Honeywell. I finally called in to our HVAC company through a different line (not a repair line) and asked them if they could fix this. They said yes they would replace it...in five days. I asked if they carried any other brands than the one they installed and they didn't. Frustrated I decided to runaway from the problem and went out to mow some of the muddy areas of the yard with the riding mower.
Now our mower is an commercial grade mower that we had to buy because someone keeps running into stuff bending the deck on regular mowers. I won't say who that someone is, but it's not me and it's probably my wife. Because of this, the mower weighs 1400 lbs. (about 650Kg) and because of its massive weight it gets stuck if there is any amount of moisture on the ground. While attempting to mow the parts of the yard that were too wet before, I hit a puddle or moss or gnat pee, whatever it was, the mower became hopelessly stuck. Now for reasons that I won't go into right now, I am the only one currently able to run this mower, so there was no one to drive the mower while I attempted to pull it out. So I did one any red blooded American male would do that has a Jeep and at least one ball (which I barely qualify for), I hooked up the Jeep and dropped it in four wheel drive low and jerked the crap out of it. You may have seen in the news where the day was .25 seconds shorter yesterday, that's because the massive torque of my Jeep pulling out this mower actually stopped the Earth's rotation for a brief moment. After these shenanigans were done, it was pretty much too late to attempt the ditch mowing/incision ripping yesterday.
So today I got up and went to a hardware store to find a thermostat that didn't have "Honeywell" stamped on it. I found one and then had to pick up a bag of concrete for another project we are doing. I found the correct type of concrete (for the record, there are approximately 75 different types of concrete and no matter what your project, there will be exactly 1 (one) bag that kinda fits what you are needing to do, and it will be on a very high shelf). I look straight at the bag...literally, because someone at Home Depot decided that this particular type of concrete needed to be about five feet in the air, and it dawned on me as I read "80 lbs." on the side of the bag that: A) I haven't lifted 80 lbs. since my surgery, I am officially supposed to be closer to 30lbs., and B) I can't bring the Jeep in to help me with this one. I briefly thought about asking for help, but two things occurred to me: 1) Guys are not supposed to ask for any sort of help whatsoever in a hardware store unless it is a veiled attempt to prove they know more than the person they are talking to, and 2) I have about as much chance of finding and employee at Home Depot to help me as I do of finding the Loch Ness Monster, Elvis, Jimmy Hoffa, and a regular cast member from Alf. Now Andrea Elson did walk by while I was contemplating the next move, but without Elvis, Jimmy, and Nessie she wouldn't have been much help. So I did what any self respecting guy would do, I picked up the bag anyway, rather than get help, and waited for the "pop" down below. I firmly grabbed the bag and just as gracefully has a Olympic weight lifter clean and jerks 1000 lbs., I put the concrete in the cart...OK, it was less like an Olympic weight lifter and more like a out of shape fat guy struggling to lift more weight than he lifted in eight months (outside of Golden Corral) all the while trying not drag the bag (which they for some reason make out of paper just slightly thicker than tissue paper) over anything that might snag it, causing it to burst open cartoonishly burying my feet in 80 lbs. of concrete, while at the same time trying to keep me from bursting open cartoonishly burying my feet in a large pile of my intestines. Unfortunately for the person watching me on the security camera I was able to load the concrete without any comic mishaps (yes, they actually have a sign in the concrete section pointing to the security camera, maybe that is a sign you are way understaffed if someone can grab an 80 lbs. bag of concrete and no one notices nor is able to catch someone fleeing with 80 lbs. of concrete).
Eventually, I made it home and the first thing I had to do, with the air conditioner running like an out of control Trane, was replace the thermostat. The thermostat contains slightly more wires than the Space Shuttle, except with fewer directions. After approximately 47 hours of cursing, reading, taking a Spanish course, reading the other manual, taking a Hindi course, calling tech support, and some Eeny Meeny Miney Mo, I was able to hook up the thermostat with a minimum amount of smoke and sparks. As I was wrapping up, a large storm hit, effectively ending my mowing/stomach shredding/toe slicing plans for the day.
I don't know if the events keeping me from mowing the ditch are a bit of Divine Intervention or just me being lazy and slow, but I will welcome the postponements no matter what the reasons. I just don't know what I am going to break to get out of it tomorrow...
Wednesday, May 11, 2011
There's More To Recovery Than Just Recovery...
Today I spent the morning with a good friend who is recovering from her own serious health condition. We got into a conversation about how hard it is to recover from a serious illness, not necessarily physically but mentally as well. There are so many aspects to recovery that get overlooked because caregivers are focused on, well recovery, but just physical. The medical profession seems to think if they fixed your ailment, you're done.
One thing I noticed since my cancer diagnosis, is before I found out I had cancer, I did routine checks for testicular cancer. I had a doctor in 1998 tell me it would be a good idea to check and I did the checks often, sometimes twice or more a day depending on how many other people were in the pool at the time, but every since I found the cancer, I hardly check. The ironic thing is, I have about half as much to check after the cancer, so you would think it would be easier to check now. However, I could probably count the times I have checked since then on one hand...not that hand the other one, the non-checking hand. I don't know why, but I have developed an aversion to checking myself since I had actually found something. Luckily, since I still manage to see one professional or another approximately every forty three minutes, I am getting checked enough right now by other people, so I don't need to worry about it, my family doctor, my urologist, my oncologist, my friend's overly curious dog, that TSA guy behind me in line at Arby's the other day, well at least I think it was a TSA uniform, or it could have been a bus driver's uniform, who ever it was he was very gentle and paid for my Arby-Q. I brought this issue up at my cancer support group to see if any other of the self examiners had the same mental block after diagnosis, but unfortunately the breast cancer survivors weren't there that day. There were a few prostate cancer survivors, but they didn't look flexible enough to perform self exams.
When down physically for so long, it takes a while to get back in the swing of things. The doctors pretty much force you to be a couch potato through weight restrictions and other warnings of dyer consequences if you overexert. After weeks, or even months, of continuously watching daytime TV, it's hard to get back into a routine of getting up, moving around, and even concentrating on anything that doesn't involve paternity testing, especially during Oprah's last season! And even when you do start to move about and get braver and braver, there can be certain obstacles in your daily life that look insurmountable. As part of my mowing routine, I have to dangle a push mower down a very steep embankment about five feet, pull it back up, and try to keep my toes out of the way the whole time I am struggling with it. This is something that leaves me physically drained and crippled on a good day, I will admit, I am scared to death to do it when I still haven't been released to do that sort of thing from the doctor that performed my surgery.
Then there is just the mental recovery. Believe it or not, you feel like your brain gets flabby from not being used while you were recovering. I tried to keep my brain sharp by first reading Yahoo articles on-line, then working my way up to on-line versions of magazines, then newspapers, and even tried to read a few books on-line. It was months into my recovery before I realized I had just been looking at porn the whole time, which I would stop, but I am not quite done with this article. The point being, when you brain isn't working as hard as it had in the past, it takes a while to be able to stare at a computer screen for hours on end again (especially if there is no porn on that computer screen).
One last part of mental recovery I will mention, kinda relates to one of the first things I mentioned, and that is the fear that you are not quite well yet, or that it will come back. There is a reason that until recently, oncologists would never use the word "cured" they would just say "remission". I don't know that I will ever get over the fear that the cancer isn't quite gone, or that it's hiding somewhere else, or that it's just not big enough to show up on tests yet, or that it's lying dormant, or, or, or, or....with so much of cancer being an unknown, how do we as patients feel secure in our "cured" diagnoses? And am I sure our families/caregivers/support networks have the same fears, whether they will verbalize them or not.
I guess in many ways, recovering from a serious illness is like a "recovering alcoholic". Sure, Bill W. never plans on having another drink, but he knows that threat is always lurking in the background. In much the same way, I don't ever plan on having cancer again, but I know there is a possibility, however slight, that it could be hiding somewhere. Maybe I should do some more internet "reading" and a self-exam just to make sure there's no cancer left.
One thing I noticed since my cancer diagnosis, is before I found out I had cancer, I did routine checks for testicular cancer. I had a doctor in 1998 tell me it would be a good idea to check and I did the checks often, sometimes twice or more a day depending on how many other people were in the pool at the time, but every since I found the cancer, I hardly check. The ironic thing is, I have about half as much to check after the cancer, so you would think it would be easier to check now. However, I could probably count the times I have checked since then on one hand...not that hand the other one, the non-checking hand. I don't know why, but I have developed an aversion to checking myself since I had actually found something. Luckily, since I still manage to see one professional or another approximately every forty three minutes, I am getting checked enough right now by other people, so I don't need to worry about it, my family doctor, my urologist, my oncologist, my friend's overly curious dog, that TSA guy behind me in line at Arby's the other day, well at least I think it was a TSA uniform, or it could have been a bus driver's uniform, who ever it was he was very gentle and paid for my Arby-Q. I brought this issue up at my cancer support group to see if any other of the self examiners had the same mental block after diagnosis, but unfortunately the breast cancer survivors weren't there that day. There were a few prostate cancer survivors, but they didn't look flexible enough to perform self exams.
When down physically for so long, it takes a while to get back in the swing of things. The doctors pretty much force you to be a couch potato through weight restrictions and other warnings of dyer consequences if you overexert. After weeks, or even months, of continuously watching daytime TV, it's hard to get back into a routine of getting up, moving around, and even concentrating on anything that doesn't involve paternity testing, especially during Oprah's last season! And even when you do start to move about and get braver and braver, there can be certain obstacles in your daily life that look insurmountable. As part of my mowing routine, I have to dangle a push mower down a very steep embankment about five feet, pull it back up, and try to keep my toes out of the way the whole time I am struggling with it. This is something that leaves me physically drained and crippled on a good day, I will admit, I am scared to death to do it when I still haven't been released to do that sort of thing from the doctor that performed my surgery.
Then there is just the mental recovery. Believe it or not, you feel like your brain gets flabby from not being used while you were recovering. I tried to keep my brain sharp by first reading Yahoo articles on-line, then working my way up to on-line versions of magazines, then newspapers, and even tried to read a few books on-line. It was months into my recovery before I realized I had just been looking at porn the whole time, which I would stop, but I am not quite done with this article. The point being, when you brain isn't working as hard as it had in the past, it takes a while to be able to stare at a computer screen for hours on end again (especially if there is no porn on that computer screen).
One last part of mental recovery I will mention, kinda relates to one of the first things I mentioned, and that is the fear that you are not quite well yet, or that it will come back. There is a reason that until recently, oncologists would never use the word "cured" they would just say "remission". I don't know that I will ever get over the fear that the cancer isn't quite gone, or that it's hiding somewhere else, or that it's just not big enough to show up on tests yet, or that it's lying dormant, or, or, or, or....with so much of cancer being an unknown, how do we as patients feel secure in our "cured" diagnoses? And am I sure our families/caregivers/support networks have the same fears, whether they will verbalize them or not.
I guess in many ways, recovering from a serious illness is like a "recovering alcoholic". Sure, Bill W. never plans on having another drink, but he knows that threat is always lurking in the background. In much the same way, I don't ever plan on having cancer again, but I know there is a possibility, however slight, that it could be hiding somewhere. Maybe I should do some more internet "reading" and a self-exam just to make sure there's no cancer left.
Monday, May 9, 2011
"If I Leave You It Doesn't Mean I Love You Any Less"
For the second day in a row I am starting off with a Warren Zevon quote. While Warren was dying of mesothelioma he wrote a song to his wife with the line "if I leave you it doesn't mean I love you any less". It was a touching line when I first heard it and a much more powerful line after my cancer diagnosis. I think the first reaction when you are diagnosed, is to wonder if you are going to survive. The second reaction is if you don't survive, what will that do to your family? What a brilliantly simple way of expressing how we feel. If cancer takes us, it doesn't mean that we want to go.
I "graduated" from the Wellness Community this week. I won't say I am 100% over all of this stuff, heck for one thing I haven't officially been released from the urologist yet, but cancer is no longer the prevailing thought in my mind anymore. Granted there are other things going on in my life right now that are taking my focus off that crap, which is a good thing. I don't know if I would feel this far removed from cancer otherwise, but the point is I do and that's all that matters. It's hard to believe my cancerversary is coming up in just a few months!
The Wellness Community and more importantly the people in my support group have been very...well supportive. I was hoping there would be a big crowd there so I could say "bye", but there was only the facilitator and one other guy, who happened to be my favorite guy and the one that helped me the most. This particular guy (without giving any identifying information, which is a no-no for a support group) has lived with cancer for literally decades. Not a survivor, LIVED WITH CANCER as in still has cancer! There is another in my group that has lived with cancer for about a decade as well. Do you know how comforting that is to someone who just got diagnosed? Even if you aren't cured, here is living proof that you can live with cancer and look like a normal non-cancer-having person! And the thing I was most impressed with these two individuals was they were the most upbeat of the group. They weren't cursing their maker or bitter at the world. They were positive. With just my favorite guy in my final meeting, I was able to spend a lot of time telling him just how important he has been to my emotional recovery. I wish there were a couple of others there that I wanted to thank, but that's what e-mail is for.
Now to complain about my group for just one second. One thing I did get off my chest was there was an incredibly negative individual that almost caused me to quit the group. This person was CURED but didn't want to believe it and spent the whole meeting going on about how if you had cancer once it stays in you forever and it can pop up anytime, even if the doctor says you are in remission or even cured. That is not something I wanted to be around just out of my surgery and facing chemotherapy. Luckily, the lady from the No Boobs About It blog warned me that there is one of those people in every group, to just try to ignore them. I am glad she told me that. The only other complaint I have with my group (and people in general) sometimes when life looks the darkest, people give up on you. Most cancer patients have ups and downs in their care, and some people in the group would start referring to people in the past tense that were struggling in their fight. The whole time Monty Python and the Holy Grail was running through my head "I'm not dead yet..." All of the people referred to in the past tense have gotten better! Thank God (literally) that they had better outlooks on their own lives than some of their supporters.
But all in all, I loved the Wellness Community and the support everyone gave me. I didn't really want to leave, but I didn't feel it was right for me to be there anymore, since I feel less and less like a cancer patient and more like a cancer survivor. I wanted to thank everyone for what they did with a gift, however I couldn't just give gifts because I am still unemployed and don't have a lot of money flowing in right now. I would have liked to cook something and bring it in (and let's just pretend for a moment that my cooking is tolerable) but when you are on chemo, you can be super sensitive to tastes and smells (I still won't touch pasta and shun salt, two things I enjoyed before chemo) so food is not even allowed inside the room we meet in. So that left me with my favorite thing, music.
Not only have I worked extensively in music running record stores, as a club DJ, and even with a record company being required to hang out with rock stars for three years, but I have always used music to alter my mood and relate to others. Back in the day, years before I even met my wife (if she is reading this) I would make mix tapes and CD's to open doors to hot girls that would inevitably ask for more CDs and less of me. More recently, I boil my music collection to moods. I have several CDs I put together just to keep me awake on roadtrips. I have CDs I made to listen to just when I want to sing loud in the car with no one around. I have a CD I made to listen to when you are in a pissed off mood (which I largely gathered from my wife's music collection, I don't know what that means, I'm just saying...). And I have made CDs just to put me in a good mood. So that is what I did, I made CDs for my group, happy CDs. You know, songs that are just impossible to be sad while listening to, stuff like LFO's Summer Girls, Spice Girls' Wannabe, and Hanson's MmmBop...OK, I am lying, I like most people over the age of two and with most of their faculties hate those songs. That was just a list of my sister's CD collection. (The funny thing here, is I have to approve all comments before they are posted, so there is no way for her to refute this on my page. But I am sure there will be retribution on hers.) But I did put together a list of twenty songs from 1952 to the mid 1990s that just make you feel good. I don't know if they will appreciate them or not, but even if they don't, at least I gave them a new shiny coaster.
So Thursday, Warren's lyrics held a different meaning to me. I didn't want to leave the friendships, but it was time for me to leave the group. And although I can't specifically identify people or illnesses, I will vaguely take a moment to say some "thank yous". Thank you Bill for showing me how one person can face cancer and act like...well someone that doesn't have cancer. Thank you Susan for having that magic folder where much like a Magic 8 Ball, you ask a question, you reach your hand in, and pull out a print out with the answer. Thank you Ann for showing just how hard one human can fight, and still retain grace and dignity the whole time. Thank you Cary for taking a bad situation and turning it around for something good. And most of all thank you Ned, no doubt your family sacrificed a great deal for the benefit of so many others, and I will never be able to express my gratitude sufficiently. And there are many others at the group that helped me, and I don't mean to play favorites here...but I am (did). And it's not like anyone actually reads these anyway, so there is not really anyone to offend with an omission. Even though I didn't place that Warren Zevon song (Keep Me In Your Heart For A While) on the CD I made, because although very poignant and beautiful it's also incredibly depressing, I graduate from and depart the Wellness Community with those words in my heart and mind, "If I leave you it doesn't mean I love you any less".
I "graduated" from the Wellness Community this week. I won't say I am 100% over all of this stuff, heck for one thing I haven't officially been released from the urologist yet, but cancer is no longer the prevailing thought in my mind anymore. Granted there are other things going on in my life right now that are taking my focus off that crap, which is a good thing. I don't know if I would feel this far removed from cancer otherwise, but the point is I do and that's all that matters. It's hard to believe my cancerversary is coming up in just a few months!
The Wellness Community and more importantly the people in my support group have been very...well supportive. I was hoping there would be a big crowd there so I could say "bye", but there was only the facilitator and one other guy, who happened to be my favorite guy and the one that helped me the most. This particular guy (without giving any identifying information, which is a no-no for a support group) has lived with cancer for literally decades. Not a survivor, LIVED WITH CANCER as in still has cancer! There is another in my group that has lived with cancer for about a decade as well. Do you know how comforting that is to someone who just got diagnosed? Even if you aren't cured, here is living proof that you can live with cancer and look like a normal non-cancer-having person! And the thing I was most impressed with these two individuals was they were the most upbeat of the group. They weren't cursing their maker or bitter at the world. They were positive. With just my favorite guy in my final meeting, I was able to spend a lot of time telling him just how important he has been to my emotional recovery. I wish there were a couple of others there that I wanted to thank, but that's what e-mail is for.
Now to complain about my group for just one second. One thing I did get off my chest was there was an incredibly negative individual that almost caused me to quit the group. This person was CURED but didn't want to believe it and spent the whole meeting going on about how if you had cancer once it stays in you forever and it can pop up anytime, even if the doctor says you are in remission or even cured. That is not something I wanted to be around just out of my surgery and facing chemotherapy. Luckily, the lady from the No Boobs About It blog warned me that there is one of those people in every group, to just try to ignore them. I am glad she told me that. The only other complaint I have with my group (and people in general) sometimes when life looks the darkest, people give up on you. Most cancer patients have ups and downs in their care, and some people in the group would start referring to people in the past tense that were struggling in their fight. The whole time Monty Python and the Holy Grail was running through my head "I'm not dead yet..." All of the people referred to in the past tense have gotten better! Thank God (literally) that they had better outlooks on their own lives than some of their supporters.
But all in all, I loved the Wellness Community and the support everyone gave me. I didn't really want to leave, but I didn't feel it was right for me to be there anymore, since I feel less and less like a cancer patient and more like a cancer survivor. I wanted to thank everyone for what they did with a gift, however I couldn't just give gifts because I am still unemployed and don't have a lot of money flowing in right now. I would have liked to cook something and bring it in (and let's just pretend for a moment that my cooking is tolerable) but when you are on chemo, you can be super sensitive to tastes and smells (I still won't touch pasta and shun salt, two things I enjoyed before chemo) so food is not even allowed inside the room we meet in. So that left me with my favorite thing, music.
Not only have I worked extensively in music running record stores, as a club DJ, and even with a record company being required to hang out with rock stars for three years, but I have always used music to alter my mood and relate to others. Back in the day, years before I even met my wife (if she is reading this) I would make mix tapes and CD's to open doors to hot girls that would inevitably ask for more CDs and less of me. More recently, I boil my music collection to moods. I have several CDs I put together just to keep me awake on roadtrips. I have CDs I made to listen to just when I want to sing loud in the car with no one around. I have a CD I made to listen to when you are in a pissed off mood (which I largely gathered from my wife's music collection, I don't know what that means, I'm just saying...). And I have made CDs just to put me in a good mood. So that is what I did, I made CDs for my group, happy CDs. You know, songs that are just impossible to be sad while listening to, stuff like LFO's Summer Girls, Spice Girls' Wannabe, and Hanson's MmmBop...OK, I am lying, I like most people over the age of two and with most of their faculties hate those songs. That was just a list of my sister's CD collection. (The funny thing here, is I have to approve all comments before they are posted, so there is no way for her to refute this on my page. But I am sure there will be retribution on hers.) But I did put together a list of twenty songs from 1952 to the mid 1990s that just make you feel good. I don't know if they will appreciate them or not, but even if they don't, at least I gave them a new shiny coaster.
So Thursday, Warren's lyrics held a different meaning to me. I didn't want to leave the friendships, but it was time for me to leave the group. And although I can't specifically identify people or illnesses, I will vaguely take a moment to say some "thank yous". Thank you Bill for showing me how one person can face cancer and act like...well someone that doesn't have cancer. Thank you Susan for having that magic folder where much like a Magic 8 Ball, you ask a question, you reach your hand in, and pull out a print out with the answer. Thank you Ann for showing just how hard one human can fight, and still retain grace and dignity the whole time. Thank you Cary for taking a bad situation and turning it around for something good. And most of all thank you Ned, no doubt your family sacrificed a great deal for the benefit of so many others, and I will never be able to express my gratitude sufficiently. And there are many others at the group that helped me, and I don't mean to play favorites here...but I am (did). And it's not like anyone actually reads these anyway, so there is not really anyone to offend with an omission. Even though I didn't place that Warren Zevon song (Keep Me In Your Heart For A While) on the CD I made, because although very poignant and beautiful it's also incredibly depressing, I graduate from and depart the Wellness Community with those words in my heart and mind, "If I leave you it doesn't mean I love you any less".
Sunday, May 8, 2011
Enjoy Every Sandwich
I haven't spent much time on the computer lately because I was spending too much time on the computer. No, I wasn't actually doing anything on the computer, I was just watching it sit and lock up and restart. I can't complain too much, the computer I was using was from 2003. However, this week while helping a friend with a project, and sitting at the computer for literally an hour while it processed the request I was asking of it, I said enough was enough. After begging and pleading with my wife, I now have a brand new computer that actually turns on when you turn it on, and does what you ask it to do. I bought it yesterday and upon cleaning out the old computer and setting up my new one, I decided to check the speed of the thing by watching some video content that I have missed over the years. Not porn, because I make sure not to miss that, just everything from a Simpson's episode I missed last month to Warren Zevon's last appearance on David Letterman a few years back.
At my support group meeting two weeks ago, we discussed how all of us in the group, after having the inarguably life changing cancer diagnosis, all have adopted a more living-in-the-moment attitude. We were not talking about living your life like an anarchist, we were talking about living without regrets. When people say they live their life without regrets, they tend to mean that they stand by the decisions they made in their life, be them good or bad, because even bad decisions can be learning experiences. However, the living without regrets that we were referring to, is all of the times in our lives we have passed on an opportunity or not followed a dream for trivial reasons. They can be life decisions or just fun times we passed up with friends. Whether it be regretting not going to that concert with your buddy, or not having the opportunity to say "bye" to someone before it was too late, or not marrying Christie Turlington, there are several decisions in all of our lives we wish we could change or get that opportunity back.
Still unemployed, I have recently reevaluated my life and my career path. My latest career path started when I was volunteering while helping out my hometown during the floods along the Mississippi River. I loved working side by side with people to sandbag in an effort to save their house, business, church, or just the town in general. I later managed to get into the disaster business and found that in the disaster business, you don't really get to help those individuals anymore. I got more and more immersed in my job, working longer and weirder hours, seeing the people I wanted to help less and less. I got to teach disaster preparedness to people, which I loved, but my job was asking me to take a more supervisory role on that as well and have volunteers do that. When you work a job you love and you work long hours, the years go by, the job changes, and before you know it, the job you once loved, is no longer the same job, and you just love it out of habit. It dawned on me recently, that is what happened to me.
After the things that have happened in my life lately, I have analyzed what I enjoy. When you are faced with life altering events, you realize a job can be something you love doing and are willing to sacrifice for, something you hate doing, but it pays so much it gives you the opportunity to spend that money on your family enriching your life that way, for a lucky few like musicians and porn stars it could be a job that you both love and pays a lot, or it can be a job you hate, doesn't pay that well, and isn't rewarding. After talking with my wife, we both agreed that in this stage of our lives, I should look for either a job I really, really enjoy, a job that I maybe don't enjoy and doesn't pay much but allows me a lot of time with my family, or a job that pays ridiculous money that when I do get sometime off I can afford to jet off to Walt Disney World or buy expensive guitars (she says spend the money on the family, but that's not how I processed it in my mind). Just like we talked in my group, live in the moment, make sure your job is worth it to you, either monetarily or sense of accomplishment.
But we weren't just talking about jobs in my group. We were talking about everything in life, meeting that friend for lunch, dropping an e-mail to a sick friend, taking that trip, learning that skill you have always wanted, whatever. I wish I could live a week in Cinderella's Castle at Walt Disney World, get right out of bed walk straight to the Jungle Cruise and shoot an elephant in my PJs (how he got in my pajamas I'll never know...ya gotta love Groucho!). That is a trip that would probably bankrupt me and put a huge financial strain on my family for many years to come. That is not the type of thing we were talking about. However, for years my wife and I have dreamed of taking a trip out west, just driving and seeing the sights this country has to offer. That trip, I have no doubt we will take in the coming years when we are physically and financially able to go. For years, I have begged my parents to come to Florida with us. We went as a family one time and had a great experience. That was sixteen years ago. My wife and I are able to visit Florida frequently on a fairly cheap budget. I have invited my parents many times and offered many ways to help facilitate their travel down there. Time after time we are turned down and have basically heard from them that they will never travel that far again. It is something that really saddens me, especially since my cancer diagnosis. We don't know when God may call any of us back home. We don't know how much time we have with each other. Instead of just showing my parents photos and telling them what a great time we have in Florida, we would like to take them, show them, experience it with them (until they get tired and grumpy like old people tend to do, then we will lock them in a bathroom or something). I think what saddens me is not so much the repeated declines of our previous offers, but how they say they don't ever think they will make a trip like that again. I was taken to Disney Parks the first time by my family and I was kind of hoping that one day they would be there to experience it with their grandchild. Who knows, maybe they will be more adventurous by the time that opportunity rolls around, or at least senile enough that we can tell them we are taking them to Big Lots or something and Big Lots has a new one thousand mile long parking lot.
When Warren Zevon made his final appearance on David Letterman, he was well aware that he was dying from Mesothelioma. He knew it was the last time he would be on there. He knew that the breath that he drew to sing songs many people loved was being stolen more and more by the cancer filling his lungs. Warren had a great attitude and repeated many times through his dying days "Enjoy every sandwich." It may sound stupid and simple, but for anyone that has looked at a doctor waiting to hear a success rate or a chance of survivability we know exactly what he means. Do what you enjoy. Don't waste your time on things you don't enjoy. If you do have to do things you don't enjoy, make sure it's worth it in the end. Learn to love the gifts you are given in your life, the big ones and the little ones. Enjoy every sandwich. With that said, I am sore from typing and hungry for a sandwich, so it's time to get off of here.
At my support group meeting two weeks ago, we discussed how all of us in the group, after having the inarguably life changing cancer diagnosis, all have adopted a more living-in-the-moment attitude. We were not talking about living your life like an anarchist, we were talking about living without regrets. When people say they live their life without regrets, they tend to mean that they stand by the decisions they made in their life, be them good or bad, because even bad decisions can be learning experiences. However, the living without regrets that we were referring to, is all of the times in our lives we have passed on an opportunity or not followed a dream for trivial reasons. They can be life decisions or just fun times we passed up with friends. Whether it be regretting not going to that concert with your buddy, or not having the opportunity to say "bye" to someone before it was too late, or not marrying Christie Turlington, there are several decisions in all of our lives we wish we could change or get that opportunity back.
Still unemployed, I have recently reevaluated my life and my career path. My latest career path started when I was volunteering while helping out my hometown during the floods along the Mississippi River. I loved working side by side with people to sandbag in an effort to save their house, business, church, or just the town in general. I later managed to get into the disaster business and found that in the disaster business, you don't really get to help those individuals anymore. I got more and more immersed in my job, working longer and weirder hours, seeing the people I wanted to help less and less. I got to teach disaster preparedness to people, which I loved, but my job was asking me to take a more supervisory role on that as well and have volunteers do that. When you work a job you love and you work long hours, the years go by, the job changes, and before you know it, the job you once loved, is no longer the same job, and you just love it out of habit. It dawned on me recently, that is what happened to me.
After the things that have happened in my life lately, I have analyzed what I enjoy. When you are faced with life altering events, you realize a job can be something you love doing and are willing to sacrifice for, something you hate doing, but it pays so much it gives you the opportunity to spend that money on your family enriching your life that way, for a lucky few like musicians and porn stars it could be a job that you both love and pays a lot, or it can be a job you hate, doesn't pay that well, and isn't rewarding. After talking with my wife, we both agreed that in this stage of our lives, I should look for either a job I really, really enjoy, a job that I maybe don't enjoy and doesn't pay much but allows me a lot of time with my family, or a job that pays ridiculous money that when I do get sometime off I can afford to jet off to Walt Disney World or buy expensive guitars (she says spend the money on the family, but that's not how I processed it in my mind). Just like we talked in my group, live in the moment, make sure your job is worth it to you, either monetarily or sense of accomplishment.
But we weren't just talking about jobs in my group. We were talking about everything in life, meeting that friend for lunch, dropping an e-mail to a sick friend, taking that trip, learning that skill you have always wanted, whatever. I wish I could live a week in Cinderella's Castle at Walt Disney World, get right out of bed walk straight to the Jungle Cruise and shoot an elephant in my PJs (how he got in my pajamas I'll never know...ya gotta love Groucho!). That is a trip that would probably bankrupt me and put a huge financial strain on my family for many years to come. That is not the type of thing we were talking about. However, for years my wife and I have dreamed of taking a trip out west, just driving and seeing the sights this country has to offer. That trip, I have no doubt we will take in the coming years when we are physically and financially able to go. For years, I have begged my parents to come to Florida with us. We went as a family one time and had a great experience. That was sixteen years ago. My wife and I are able to visit Florida frequently on a fairly cheap budget. I have invited my parents many times and offered many ways to help facilitate their travel down there. Time after time we are turned down and have basically heard from them that they will never travel that far again. It is something that really saddens me, especially since my cancer diagnosis. We don't know when God may call any of us back home. We don't know how much time we have with each other. Instead of just showing my parents photos and telling them what a great time we have in Florida, we would like to take them, show them, experience it with them (until they get tired and grumpy like old people tend to do, then we will lock them in a bathroom or something). I think what saddens me is not so much the repeated declines of our previous offers, but how they say they don't ever think they will make a trip like that again. I was taken to Disney Parks the first time by my family and I was kind of hoping that one day they would be there to experience it with their grandchild. Who knows, maybe they will be more adventurous by the time that opportunity rolls around, or at least senile enough that we can tell them we are taking them to Big Lots or something and Big Lots has a new one thousand mile long parking lot.
When Warren Zevon made his final appearance on David Letterman, he was well aware that he was dying from Mesothelioma. He knew it was the last time he would be on there. He knew that the breath that he drew to sing songs many people loved was being stolen more and more by the cancer filling his lungs. Warren had a great attitude and repeated many times through his dying days "Enjoy every sandwich." It may sound stupid and simple, but for anyone that has looked at a doctor waiting to hear a success rate or a chance of survivability we know exactly what he means. Do what you enjoy. Don't waste your time on things you don't enjoy. If you do have to do things you don't enjoy, make sure it's worth it in the end. Learn to love the gifts you are given in your life, the big ones and the little ones. Enjoy every sandwich. With that said, I am sore from typing and hungry for a sandwich, so it's time to get off of here.
Wednesday, April 20, 2011
If Coughing Were A Sport, I Would Be An Olympian!
So a couple weeks back I wrote about having a cold. Well, the sniffling stopped, the sneezing stopped, and the coughing...well it never went away. In my typical, stubborn, I-don't-want-to-go-to-the-doctor sort of way, I decided the best thing to do was to ignore it and keep coughing. That changed the night my wife asked why I was breathing so fast. I said I wasn't breathing fast, especially since I was just sitting there, not exerting myself with heavy exercise like bending over to tie my shoes, reaching for more cookies, or grabbing the remote to change the channel. When she pointed out that I indeed was breathing fast, I started getting worried. One possible cause could be pneumonia or any other number of pfunny gnamed illknesses.
So, first thing the next day I called the doctor and scheduled an appointment for later that day. The two things I can always count on with my obsessive-compulsive doctor is that no matter what I am there for I have to be humiliated with the scale, and that he will be at the very latest on time. And that is exactly what happened, after finding out I was fat (again) I was taken back to see the doctor...early! While the nurse was pointing out that I was fat and taking my blood pressure, she scared me by telling me how rampant pneumonia has been this year. My doctor came in and had me take several deep breaths, much more than usual, which seemed like a pretty sadistic thing to do to someone that was having trouble breathing. Finally, he told me to take a deep breath, and breathe it out as fast as I could, which resulted in my coughing very hard, getting light headed, and almost falling off the exam table. That caused him to giggle a little and tell me that people usually get lightheaded if they come in in my state and do that, which made me wonder why, if most people get lightheaded and almost fall off the table, why didn't he put himself in some sort of position to catch me? Anyway, he narrowed it down to walking pneumonia or viral bronchitis, and told me to go to the hospital right away to get an X-ray.
Because of my medical past, I have been pummeled by radiation so much to the point that my oncologist wants to limit the amount of exposure I have from now on. For those that don't know, radiation builds in your body over time. It starts from the day you were born and keeps adding up until the day you die. I told my doctor that my oncologist (and his good friend) had ordered a chest X-ray as part of my six month post-chemo check-up for the next week and asked if there was anyway I could just get one set of X-rays that would take care of what both my doctor and my oncologist wanted to see (plus then I would only have to pay one co-pay). He thought that was a great idea and wrote the prescription. My doctor sent me on my way, but not without first giving me two free inhalers. He is one of those doctors that feels if drug companies are constantly going to keep coming around and bugging him, he is going to take all the samples he can, and try his best to keep from actually ever writing a prescription for anything, just give away free samples. I don't think that is what the drug reps had in mind, but I certainly appreciate it.
I rush to the hospital just in time to spend the next half an hour filling out paperwork and answering questions between coughs. I finally got in to have my X-rays done and my doctor called the next morning to say I just had bronchitis (which isn't that much easier to spell) and that it looks like I am still cancer free. I still have another week before I hear that officially from my oncologist, but the surprise X-ray and results have definitely cut down on my scanxiety this time around.
So, going on week four since all this started, I am still coughing and according to my doctor, can expect to still be coughing for another two weeks. I am thrilled. In the meantime, I will steer clear of salty foods, keep making people around me scared that I am contagious, and keep my wife and basenjis awake by hacking all through the night. Let's just call it payback for all the kicking that they supposedly do "in their sleep".
I will close by telling the story about the Evil Casket. The Evil Casket started chasing this poor girl one day. No matter where she went the Evil Casket came bouncing after her. The faster she ran, the faster the Evil Casket bounced. She ran into her house and locked the door, the Evil Casket knocked the door down. She ran upstairs, and the Evil Casket bounded right up the stairs behind her. She ran into the bathroom and locked the door, and the Evil Casket broke that door down too. Cornered and desperate, the poor girl reached for something, anything to use as a weapon against the Casket. She opened the medicine cabinet, grabbed the Dimetapp, threw at her pursuer, and....the coffin stopped!
So, first thing the next day I called the doctor and scheduled an appointment for later that day. The two things I can always count on with my obsessive-compulsive doctor is that no matter what I am there for I have to be humiliated with the scale, and that he will be at the very latest on time. And that is exactly what happened, after finding out I was fat (again) I was taken back to see the doctor...early! While the nurse was pointing out that I was fat and taking my blood pressure, she scared me by telling me how rampant pneumonia has been this year. My doctor came in and had me take several deep breaths, much more than usual, which seemed like a pretty sadistic thing to do to someone that was having trouble breathing. Finally, he told me to take a deep breath, and breathe it out as fast as I could, which resulted in my coughing very hard, getting light headed, and almost falling off the exam table. That caused him to giggle a little and tell me that people usually get lightheaded if they come in in my state and do that, which made me wonder why, if most people get lightheaded and almost fall off the table, why didn't he put himself in some sort of position to catch me? Anyway, he narrowed it down to walking pneumonia or viral bronchitis, and told me to go to the hospital right away to get an X-ray.
Because of my medical past, I have been pummeled by radiation so much to the point that my oncologist wants to limit the amount of exposure I have from now on. For those that don't know, radiation builds in your body over time. It starts from the day you were born and keeps adding up until the day you die. I told my doctor that my oncologist (and his good friend) had ordered a chest X-ray as part of my six month post-chemo check-up for the next week and asked if there was anyway I could just get one set of X-rays that would take care of what both my doctor and my oncologist wanted to see (plus then I would only have to pay one co-pay). He thought that was a great idea and wrote the prescription. My doctor sent me on my way, but not without first giving me two free inhalers. He is one of those doctors that feels if drug companies are constantly going to keep coming around and bugging him, he is going to take all the samples he can, and try his best to keep from actually ever writing a prescription for anything, just give away free samples. I don't think that is what the drug reps had in mind, but I certainly appreciate it.
I rush to the hospital just in time to spend the next half an hour filling out paperwork and answering questions between coughs. I finally got in to have my X-rays done and my doctor called the next morning to say I just had bronchitis (which isn't that much easier to spell) and that it looks like I am still cancer free. I still have another week before I hear that officially from my oncologist, but the surprise X-ray and results have definitely cut down on my scanxiety this time around.
So, going on week four since all this started, I am still coughing and according to my doctor, can expect to still be coughing for another two weeks. I am thrilled. In the meantime, I will steer clear of salty foods, keep making people around me scared that I am contagious, and keep my wife and basenjis awake by hacking all through the night. Let's just call it payback for all the kicking that they supposedly do "in their sleep".
I will close by telling the story about the Evil Casket. The Evil Casket started chasing this poor girl one day. No matter where she went the Evil Casket came bouncing after her. The faster she ran, the faster the Evil Casket bounced. She ran into her house and locked the door, the Evil Casket knocked the door down. She ran upstairs, and the Evil Casket bounded right up the stairs behind her. She ran into the bathroom and locked the door, and the Evil Casket broke that door down too. Cornered and desperate, the poor girl reached for something, anything to use as a weapon against the Casket. She opened the medicine cabinet, grabbed the Dimetapp, threw at her pursuer, and....the coffin stopped!
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