Lots of people ask me what I do with my free time these days. I tend to avoid going into detail when I answer this question, but since I haven't written a substantive post in a long time, I would like to give you a "Day in the Life" of Dan Fritz. It's challenging for me to talk about how I am doing in terms of physical condition day to day as opposed to what my prognosis is, since my physical condition is very rarely anything approaching pleasant. Ever since my fourth hospitalization for treatment (i.e. the second full "cycle"), my prognosis has been very positive. This is something for which I am indescribably thankful. The chemo therapy has been effective at combating the cancer, and I am confident that I will (to put it bluntly) survive and recover fully, never to deal with this type of cancer again. But while saying that, I don't want to give the false impression that I actually feel well on a daily basis. This is merely being straight forward about what it's like every day. You can see why I might not want to rehash that when talking to someone--I don't really want to think about it, and I don't want to kill the conversation by repeatedly reporting unpleasant things. Nevertheless, the following is my life these days. Maybe it will give you an idea of what chemo therapy is actually like.
My treatment works in three-week "cycles" (not to be confused with the treatment cycles, which are two hospitalizations, lasting about six weeks total). For all intents of purposes, part A of my treatment is no different than part B. Both last four days at a minimum, and the remaining two weeks+ are recovery. I feel horrendous by the fourth day in the hospital, and I can't get home fast enough. I usually haven't eaten anything (maybe some jello or pudding) for two days. I actively block all thoughts of what just occurred, because the thought of having to repeat that every three weeks is horrifying to me. I spend the next few days focusing on feeling better and being able to--say--drink water normally. What does "focusing on feeling better" mean? It means that I could literally lie in bed for six hours concentrating all of my energy on combating my physical condition (fatigue, gastro-intestinal trauma, nausea) and thinking positively. I also sleep/nap quite a bit at this point. Many times I don't even feel like watching television. As proven by my online Word Twist scores, my ability to focus and my hand-eye coordination is compromised for a while, in addition to simply having no excess energy to spend. My blood levels continue to decline for another week to a week-and-a-half after leaving the hospital, so it's not abnormal for me to actually feel worse with each progressive day of recovery during that time period. Blood transfusions are the only way to counteract that feeling, and I get those on a regular basis anymore. After blood transfusions--which could easily take 8-10 hours--I feel relatively good. Before transfusions, it can be difficult to get up and take a shower. If I am lucky, and I actually do feel well (relatively), I cannot leave the house, because my immune system is compromised. I stay inside and turn on my air filter. Even though my outlook is good and I am who I am, I sometimes suffer from anxiety in the middle of the night. I wake up sweating profusely, and I have negative dreams. I sometimes try to pre-emptively strike this by taking full, deep breaths before going to sleep. Other times, I simply wake up at 3:oo am and cannot get back to sleep for as much as five hours. This is not because I'm not tired but rather because I usually have something on my mind. Susan wakes up much of the time and it turns into a (generally comedic) middle of the night slumber party. Ironically, I count myself lucky when this happens. Some other problems I face: severe upper back tension, lower back pain and throbbing (from tests and a medication called Neulasta), headaches, bla bla bla. I tell you this simply because many people actually want to know this.
By the middle of my second full week of recovery, I feel able to get out of the house, and my immune system is good enough to allow me to do that. I meet with some people and grab some Starbucks. I do almost all of my book reading during this time, and I catch up on emails much more vigorously. I get winded if I walk very far due to deconditioning, but I still maximize my mobility at that time. I start getting ideas about pet projects I want to continue working on from months prior, and I even white board a few ideas. Like Word Twist, I play a lot more online words games and Sudoku to sharpen my mind. I eat almost whatever I wish, though I still typically avoid uncooked foods, including salads. During this week, I still have to go to the doctor a couple of times, but at least I don't have mid-cycle chemo at that point (that's usually the week prior if at all). And then...and then...I have to go back for another round of treatment. It's unavoidable for me to feel bad about this, like someone who is about to be whipped yet again. I engage in a tough mental battle on the Sunday night before re-entering the hospital, but I take solace in knowing that the treatment is curative. I then go through the hospital motions again and the cycle repeats itself. So, I don't recover over the months in the usual sense. I recover for three weeks at a time and start from square one over and over again.
Unfortunately, there's not much usable "free time" in what I just described. There is a constant physical and mental struggle, which I engage with as much vigor as possible without being foolish or needing to prove my strength of will to anyone. I relate this to you simply to inform. It can be said of this whole ordeal that "it is what it is," not good or bad but merely temporarily unlucky. Life-threatening, yes--but ultimately providing some clarity of thought and a little perspective.
So, how am I doing? I'm fine.
Sunday, May 18, 2008
Subscribe to:
Posts (Atom)