Posts Tagged Cancer
Seven years and counting
Seven years ago today, I was an emotional wreck. I knew something was wrong. The thing I had dreaded and feared since my dad got sick and died a few years before was now a reality.
I didn’t have an official diagnosis yet, but I knew. A few weeks prior I had been at the Y, really pushing myself. What felt like a good workout quickly turned into a severe pain in my lower abdomen. As I was poking around trying to figure out what was wrong, my hand grazed something hard that shouldn’t be there. I immediately recognized what it was, but didn’t want to admit it to myself.
Cancer.
It took a couple of weeks of sleepless nights before I made an appointment to see the doctor. Even then, I was too afraid to bring it up, instead asking for something to help with my insomnia.
Finally, the Thursday night before Memorial Day weekend, it came to a head. I could no longer ignore it – I either had to face the truth, or it would kill me.
I don’t generally believe God speaks to us in an audible voice – at least I’ve never experienced that. But as I prepared to call my mom to let her know what was going on, I felt His presence in a way I haven’t before or since. If I could put words to that presence, it would be “Don’t worry – I am with you. We will get through this together.”
I won’t go through the whole ordeal again, as I’ve blogged extensively about it in the past. But I feel compelled to document where I am around my cancer anniversary every year. While there are other days I could celebrate – the last day of chemo, the first day my tumor markers dropped to the normal zone, the day I was given the all-clear by the oncologist – I choose to celebrate the anniversary of my diagnosis. It’s the day that changed my life permanently – I became a cancer patient, and eventually a cancer survivor.
Going through a serious illness has a way of bringing your life in laser-sharp focus. The week after my first round of chemo, I was at a neighbor’s pool (oblivious to the fact that chemo makes you much more likely to get sunburned… but I digress). As I was trying to relax and ignore the waves of nausea and heartburn, I was thinking about my life and what I wanted out of it. I always wanted to be a husband and a father, but at that moment it became my primary goal. As I am realizing more and more every day, life is short. But it’s too long to go through alone.
I think back to that day, and look at where I am now. Seven years later, I’m a couple of weeks away from celebrating my first Father’s Day. I am blessed with two of the most amazing girls one could ask for – my wonderful wife and my adorable daughter.
Life is good.
Purdue researchers develop technology to detect cancer by scanning surface veins
Of course, they discover this *after* I was given a clean bill of health… now if they could just figure out a way to give chemo without needles.
A new technology for cancer detection that eliminates the need for drawing blood has been developed by Purdue University researchers.
Researchers from Purdue’s Cancer Center, Department of Chemistry and Weldon School of Biomedical Engineering collaborated with cancer and biotechnology experts from the Mayo Clinic to develop technology to detect tumor cells within the human body. By shining a laser on surface veins, such as those on the wrist and inside the cheek, researchers are able to reveal and count circulating tumor cells.
2nd Anniversary
Today marks the second anniversary of my cancer diagnosis. Not much to add other than that… check the archives for the full story:
Part One
Fin (Part Three)
Posted by Lane in Cancer, Politics & Religion on September 13, 2004
Vegas
So thankfully, my white blood cell count was back up to normal by the time I left for Las Vegas. Otherwise I would’ve had to inject myself with the Neupogen, and that simply wasn’t going to happen.
But of course, *something* had to come up while I was on the trip… For whatever reason, I started worrying about having cancer on the other side as well. It’s rare, but it does happen – though usually not at the same time. So I spent the better part of the trip constantly worried about that. After consulting with the urologist, he confirmed that they did check during my initial exams, and there were no signs of carcinoma in situ.
All that worrying combined with exhaustion from the chemo, the heat in Vegas (113 degress!), and all the walking we did, *AND* the indigestion I was dealing with, it wasn’t the ideal vacation. But all things considered we had a good time, and I won $80 in one hand of video poker, so I can’t complain too much.
Round Deux
As soon as I got back, I started the second cycle… another week of 6 hour days and liters upon liters of IV drips, followed by three weekly Bleo treatments. They checked my AFP levels for the first time since I started chemo, and it had dropped to 20, which was great news – the drugs were definitely doing their job.
The days all kind of run together in my memory at that point – nothing particularly memorable happened. My white and red blood cell counts were low, but stayed in the safe range, so I didn’t need any more shots. Still, the needles for getting my chemo wasn’t getting any easier. Today, I can deal with needles as long as I’m feeling well, but when I was already queazy, it’s much more difficult getting stuck.
The weekend after the first week of the second and third cycles weren’t as bad as the first, as I knew what to expect and didn’t have the bad indigestion pains like I did the first go-round (Thank you Nexium!)
During the second and third cycles, once they got the IV going, I usually went straight to sleep – at least until they hit me with the diuretic, then it was to the restroom every 20 minutes. I saw a lot of people come and go in the Circle o’ Death, most of whom were much worse off than me. There was the man who came in with his wife and daughter, where I heard that he was stage IV (the worst), and his blood counts were simply too low to handle any more chemo. I don’t know what happened to him, but outside of a miracle, he’s probably dead now. And the guy who not only had cancer, but full blown AIDS as well. And all the lung cancer patients, who will never be cured – they can only hope to extend their lives by a few months or years. In comparison, I had it easy – 12 weeks, and chances are I’m cured for good. While I had my down moments, by and large I just couldn’t feel too sorry for myself. I imagine most of the other people there would trade places with me in a heartbeat.
When I wasn’t getting pumped full of drugs, I spent most of my time at Mom’s house… watched a lot of TV, simply because there wasn’t much else I could do. Using the computer or playing video games made me sick to my stomach after a short while – something about the motion of the screen. But even TV grew old quickly. I watched so much Game Show Network and Learning Channel. And Futurama – lots of Futurama. Entire TV seasons on DVD is the greatest thing ever. Unfortunately this was also around the time that you couldn’t get away from the Affleck/Lopez saga… I swear, you couldn’t go an hour without hearing *something* about them. Yeah, that was one relationship that stood the test of time…
I never really noticed the “metallic” taste in my mouth that chemo patients often experience. But nothing really tasted good either – everything was just bland. I made the mistake of eating a lot of everything in the hopes that *something* would taste good. It rarely did. Unfortunately, the calories still counted, so over the course of my treatment my weight jumped from 188 to over 210 – and I’m still having trouble losing that extra weight.
The third cycle started in early August, and went relatively smoothly. The second cycle of chemo drove my AFP down even further – around 9, if I remember correctly. Still a little bit on the high side, but nothing to be worried about. I was essentially in the clear.
Remission
So September 4th rolled around, and I went in for my final treatment. It was rather anti-climactic, but I was just happy to be done! Of course, that night the chemo side effects were the worst they had been in at least a month, but the next day I was feeling better. No more needles for at least a month, and hopefully no more chemo EVER!
Though as soon as I thought I was in the clear, we had a scare after my one month checkup… my AFP levels were up. The normal range for AFP is below 8.5 Mine was close to 11. I didn’t think it was anything to be concerned about (as I had read that anything under 20 was good), but the doctors were worried about it. They admittedly hadn’t had much experience with testicular cancer patients, so they wanted to err on the side of caution. I went to see a specialist at Vanderbilt, who said it wasn’t anything to worry about. As long as it wasn’t moving steadily upward, some fluctuation was normal.
About that time I also developed peripheral neuropathy – a numbness in the feet and hands. It wasn’t too severe, although it made playing guitar somewhat painful. Thankfully it went away after a few months.
In October my hair started growing back – I remember going to a movie one Saturday night, and noticing all these tiny light hairs in the restroom mirror – I missed a good 10 minutes of the movie just admiring my new follicular growth. It came in slowly at first, but by my birthday on the 22nd, you could tell that I actually had a hairline. It was a pretty low-key birthday – just me, Mom, and Molly – but I was happy just to have another one.
My October and November check ups went OK – I was still tired all the time, but I didn’t worry too much about it. I had read of other cancer patients who felt the effects of chemo as much as a year after the fact. In December I started working out again, and by Christmastime, I was starting to feel more like my old self. But that didn’t last very long – in February and March I started feeling more and more run down. I would sleep for a full 12 hours every night, and a lot of my body hair that I had regrown after the chemo was starting to fall out again. Thanks to the Testicular Cancer Resource Center website, I knew that this was a sign of low testosterone. Approximately 1/3rd of all testicular cancer patients deal with this… I had my levels checked, and sure enough, I was running on empty. In April I started on Angrogel, a testosterone supplement. While I still get tired more quickly than I used to, it has helped quite a bit.
After the Fact
So here I am, a year after the fact, but it seems like it was just yesterday. While I am well in remission and probably won’t have a recurrence, I don’t want to use the word “cured”. For example, on the TC listserv I’m on, out of 607 members, five have died from testicular cancer in the past two months. Some lived 20 years after their initial diagnosis, some only a handful of months. Which just goes to show that no matter how effective the treatment is, cancer is a devious, devastating disease which refuses to go away quietly. All things considered, I am incredibly fortunate, but nothing is 100%. I realize that I’ll probably die from cancer – if not testicular cancer, some other form. But I’m OK with that. If I live for another 31 years, I’ll be very happy.
My family was such a source of strength through all this. I can’t imagine having to go through something like this alone. I’m especially grateful for my mom, who not only took care of me, but also took care of her mother during that time *and* taught school during the day. If I were in her place, I don’t think I could have handled it – but she did.
Physically I’m doing OK – I still need to lose a dozen or so pounds which refuse to come off, and I’ve lost a lot of muscle mass compared to where I was last May. But it’ll all come around eventually. I’ve moved closer to work, so I have more time during the day to exercise now. My hair, which grew back in curly, has gone back to it’s regular state.
Mentally and emotionally, it’s a mixed bag. On one hand, I’m over my fear of having cancer. Sure, I worry about it returning, but it’s not the crippling fear I had before. As I said in the first part, it wasn’t dying that scared me – it was the chemo and the needles. And now that I’ve gone through it, I know I can do it again if I have to.
On the other hand, I still worry and get upset about petty things. I get angry a lot quicker than I used to. And that makes me mad
You think of cancer being a life-altering event, which it is. It really drives home the point of how fragile life is, and how short our time is here on earth. Yet I spend way too much time worrying about my job, getting mad at the people in traffic, wondering if I’ll always be alone, etc. None of that should matter, but it does. We just fall back into our usual patterns far too quickly.
With all of that being said, the biggest thing I’ve learned is that God is in control. Even if I don’t believe that every moment of every day, or at least behave like I don’t, I know that he is there when we really need him. A few years ago I read somewhere that God will send a storm at 30 so we can handle a hurricane at 60. I’m not sure I want to know what awaits me at 60, but I now know that through Him, I can handle anything.
Whew – well, that’s all folks. Hopefully that is the end of my cancer saga!
Cancer Story Part 2: Weedkilla
The Circle of Death
This time last year, I was on my mom’s couch, feeling as if I had been run over by a truck. Thankfully, it was from the last chemo treatment I would have to endure. Hard to believe it’s been a year since then.
On June 16th, 2003 I showed up at the oncologists’ office bright and early for my first treatment. I was led to the back, to an area where about a dozen chairs were arranged in a semicircle, about half of them occupied by others already hooked up to their chemo drips. I thought to myself “Hey, it’s the Circle of Death”. Nothing like a little gallows humor to take the edge off. I took the last remaining recliner and waited for one of the nurses to get to me. I wasn’t sure what to expect – I knew I had to have blood drawn, an IV drip for the chemo, and a shot for some more chemo.
Thankfully, they were able to do everything with one stick… one of the nurses got the IV going, from which they drew blood to check my white and red cell count (more on that later), as well as my tumor markers. The two main markers they check in TC cases are AFP (Alpha-fetoprotein), and Beta-hCG. In my case, the AFP levels were high, indicating that cancer cells were still in my system. Over the course of my treatment and afterward, they would track it to gauge the effectiveness of the chemo, and to look for signs of recurrence.
Next, they started with the various and sundry IV bags… steroids and anti-nausea medicine to start. I was never quite sure what the steroids were for, and all they really did was make my face flushed. After the second day they eliminated the steroids completely.
Then came the “weed killers”: Bleomycin, Etoposide (VP-16), and Cisplatin, or BEP for short. The Bleomycin didn’t take very long – maybe 15 minutes. But the VP-16 and Cisplatin were mixed in with literally liters of saline. The stuff is pretty toxic, so it needs to be flushed out as soon as possible. To accelerate the process I was also given a diuretic (which made me feel like I had been punched in the kidneys), and found myself heading to the bathroom several times, IV pole in tow.
To push all those drugs and saline through me took a while… the first day I was there from 8:30 in the morning until 3 in the afternoon. Which was pretty much par for the course… sometimes it would only take four hours, sometimes over six. It was funny hearing the other people comment on all the large bags hanging off the IV rack, considering most of the other patients only had one or two small bags at most, and weren’t there for more than an hour.
I brought my backpack full of goodies each day – books, magazines, Gameboy, music, etc. And by the end of the week, I slept more than anything. Still, it was so boring – very little to do. Mom stayed with me most of the time that first week – I can only imagine how boring it was for her – she didn’t even have the benefit of the needles, drugs, and constant trips to the bathroom!
The Downward Spiral
The first day I felt pretty good. Went to play guitar at a youth event with John and Kevin, and played a little basketball afterwards. The next day, I was a little more worn out, but still didn’t feel “sick”. But by Wednesday I was thoroughly exhausted – I had to go into work for an hour or two to take care of some stuff, then went home and promptly fell asleep.
I was done with the first round of the BEP on Friday, which was a good thing because I felt like death warmed over. By that point, I was having all kinds of issues. There wasn’t one particular symptom that really bothered me, but the combined effects made life pretty miserable.
Just for starters, nausea was a constant – thankfully, I never vomited though. Sore throat, indigestion, tinnitus, headache, constant hiccuping. Nothing tasted good, nothing smelled good (in fact, the lotion/perfume/hairspray my mom and sister put on that Sunday nearly did make me throw up), and every sound was ear-splitting. I couldn’t watch TV or use the computer for very long, as any fast motion would make me more nauseous than usual. Add all that to just plain feeling sick – very sick. The worst part during that weekend was that I couldn’t eat – I was hungry, but nothing sounded good. When I did try to eat, it felt like the food was stuck halfway down – it’s hard to describe it exactly, but it was incredibly uncomfortable. The worst part is that there really isn’t anything you can do – you just have to deal with it.
Though that first weekend was terrible, there was a bright spot. On Saturday night, as I was trying to sleep, I felt God’s presence, even stronger than the night I accepted the fact that I had cancer. It was comforting – in the midst of this, every other concern was burned away – all that mattered was that He was in control. I knew I wasn’t alone, and that no matter what He would be there.
I spent the entire weekend in bed or on the couch at Mom’s. That Monday I had to go in for a checkup and another treatment. Thankfully it wouldn’t take half a day like the previous week. For the next three weeks, I only had to go in once a week for the Bleomycin. That first day though, I was still feeling very ill. Mom and I waited for what seemed like forever for the doctor to see me – he said I was doing very well all things considered. I can only imagine what it felt like for anyone who went through that and *didn’t* do well. He wrote a prescription for a couple of things that did help with my indigestion/heartburn thing and my hiccuping. The makers of Nexium are rolling in the dough – $5 a pill!
Second Verse, Same as the First
Anyway, I nearly passed out yet again when they got the IV going… bleh. But thankfully it was over for at least a week. That afternoon I went swimming. What they neglected to tell me is that the chemo would make me sensitive to sunlight. So on top of everything else, I had a sunburn that second week. I didn’t start feeling “normal” until the end of the second week – by that time most of the symptoms had gone away or at least faded somewhat.
That second week I also got a haircut. It was pretty much a given that my hair would go in the next week or two, so Mom thought it would be less messy if I got it chopped. It looked pretty good, I thought – I’m probably going to get it cut like that again next time I need a haircut.
I weighed myself on Wednesday of the second week. I was down to 187 – the lightest I had been since sometime in 2000. Unfortunately, I would only gain weight from that point.
Who Loves Ya Baby?
The third week I went back to work for at least a few hours each day. About that time my hair started falling out. I would run my hand through my hair and come up with a handful each time. It was kind of funny, actually. By Wednesday I had obvious bald patches, so I took the clippers, set them to the lowest height and took off most of my hair. The remaining patchy hair just *screamed* “Cancer Patient”, so I grabbed my Gillette Mach 3 and proceeded to remove it all for that classic Kojak look. I thought it looked pretty good, all things considered. For the next few months, people regularly guessed my age to be much lower than it actually is. I suppose if you don’t have a hairline to give away your age and no facial hair either (the chemo affected most of my body hair), you do look pretty young.
That Tuesday when I went to get my next Bleo treatment, my blood counts weren’t good. My white cell count was very low, which meant I was susceptible to infections that could seriously affect my treatment. So they wanted to get those numbers back up before giving me the chemo. For the next three days I got shots of Neupogen (yeah – more needles!) which kickstarted my bone marrow to produce more white blood cells. It felt similar to those growing pains when I was 13 or 14. On Thursday the numbers looked good enough, so they gave me another shot of Neupogen, as well as the Bleomycin.
That was the single worst day during the entire treatment. I went to my house, *intending* to play some Xbox, but all I could do was lay on the couch. I’m guessing that the combination of Bleomycin and Neupogen didn’t react well to each other. I would have these painful spasms in my back, my stomach, my legs, everywhere. Just out of the blue I’d have a shooting pain somewhere in my body. I’d readjust my body, which would help a little, then as soon as I relaxed, the pain would reappear somewhere else. On top of that, I had terrible chills… it was the middle of June, and I have the heat on, wearing a sweatshirt and a stocking cap. I eventually got the idea to take a hot bath, which did help tremendously – over the next few months, I would take *lots* of hot baths.
Thankfully I was feeling better by the next day. The Bleomycin was pretty rough, but usually the ill effects would only last a day, as opposed to the full BEP. Which is good, because I was heading to Vegas!
Well, I guess there will be a part three… stay tuned, true believers.
Not just another bum
Ah come on, Adrian, it’s true. I was nobody. But that don’t matter either, you know? ‘Cause I was thinkin’, it really don’t matter if I lose this fight. It really don’t matter if this guy opens my head, either. ‘Cause all I wanna do is go the distance. Nobody’s ever gone the distance with Creed, and if I can go that distance, you see, and that bell rings and I’m still standin’, I’m gonna know for the first time in my life, see, that I weren’t just another bum from the neighborhood.
OK, so it’s a little melodramatic, but I’m always looking for an excuse to quote “Rocky”
I have the opportunity to audition for Tait tomorrow. I don’t think I have a realistic shot of getting the gig, knowing how many far more talented guitarists than I live in Nashville, but I’d just like to do well and make a good showing. At the very least I can say I gave it my best shot
Right now I just want to get it over with, because my fingertips look like ground beef!
Regardless if I get the job or not, next week will be a big one… I close on my house Monday, and Friday will mark a year since my last chemo treatment. I *swear* I’ll write the second part of the cancer story soon. It’s been a very busy summer.
Tour de Lance
Posted by Lane in Cancer, Current Events on July 25, 2004
PARIS (July 25) — Lance Armstrong rode into history Sunday by winning the Tour de France for a record sixth time, an achievement that confirmed him as one of the greatest sportsmen of all time. His sixth crown in six dominant years elevated Armstrong above four champions who won five times. And never in its 101-year-old history has the Tour had a winner like Armstrong – a Texan who just eight years ago was given less than a 50 percent chance of overcoming testicular cancer that spread to his lungs and brain.
Update
Well, I managed to sell my house and get the $$$ I wanted for it. I would have preferred more, obviously, but I’m happy with what I got. Last weekend Mom and I moved a lot of the smaller stuff into my apartment, and Friday the movers are going to get all of the big stuff. Then I close on the 28th, get my check, and then can pay off my car!
I also got the results back from my latest cancer checkup, and my tumor markers are lower than they’ve ever been. It doesn’t make much difference as long as they’re not moving upwards, but lower is better
May 23, 2003
Yesterday I celebrated my one year cancer anniversary. A somewhat strange event to memorialize, but it’s been a somewhat strange year.
History and Hypochondria
While I was diagnosed a year ago, the story starts a few years earlier. My dad died after a six year battle with cancer in early 1999. His father died from cancer six years before that. Somewhere along the line I started worrying about getting cancer myself, to the point of turning into a hypochondriac – in late 2000 I was convinced I had melanoma (skin cancer) – to the point that I could literally feel my enlarged lymph nodes… it also had the very real effect of causing a flare-up of tinnnitus (chronic ringing in the ears), which can happen during times of stress.
Anyway, after a series of doctor’s appointments, I was assured that there was nothing wrong with me (except for the tinnitus). Knowing my worry about cancer, our family doctor said that the only thing I really needed to worry about at my age was testicular cancer. He checked me for that, said I had nothing to worry about, and sent me on my way with a prescription for an anti-depressant.
Over the next couple of years, I would occasionally have those irrational fears come to the surface, usually during times of stress or depression. But they would go away after a week or two.
In early 2003, an online acquaintance was diagnosed with testicular cancer. Hearing about his experience once again caused me to worry, so I checked myself for any lumps on a regular basis, but never found anything. So again, the worries passed.
About that same time I started a pretty serious workout/diet program to lose the pounds I put on over the winter. Things were going well, and I was feeling good. Losing weight at a fairly regular pace, then near the end it really dropped off rapidly, despite the fact that my diet had reverted back to fast food twice a day… I thought I was doing well with my workouts!
Fears Confirmed
In retrospect, it was probably a sign of impending doom (cue ominous music). On Saturday, May 3rd I was having a nice, long workout… tried some decline dumbbell presses, which can strain your abdomen if you’re not careful. I went home and took a shower, and just didn’t feel well at all – I had a dull ache located in my lower abdomen, and felt queasy – as if I had just gotten off a roller coaster. While I was trying to locate the center of the ache, my hand brushed against my right testicle. Something didn’t feel right, but I quickly pushed it out of my mind… I had a Def Leppard concert to go to!
While the ache went away, my mind started bringing the possibility of testicular cancer to the forefront. As always, I told myself that this was just an irrational fear, and I needed to push it aside. But every time I would be in the shower and do a partial check (being sure to stay away from whatever I felt earlier), it was obvious something was wrong. The fear and stress continued to mount for a couple of weeks – I told a friend of mine that I was afraid I might have cancer, but I knew it was probably just those old worries coming back.
The next day at church, the theme of the message was prophetic in a sense – I don’t remember the specifics, but the gist of it was that during times of suffering, we do not see the bigger picture… God’s plans, while always serving the greater good, sometimes involves personal pain. Given my anxious state of mind, this was the last thing I wanted to hear… I left halfway through because I couldn’t take it anymore.
Denial, Anger, Bargaining, Depression, Acceptance
The following week I hardly slept – spent most of the nights watching movies… Ocean’s 11 was a popular one
I cried more than once, asking God to take away the fear. I was sick and tired of being scared, and I didn’t want to be scared anymore. That Thursday I finally mustered up the courage to thoroughly check myself, knowing that what I would probably find wouldn’t be good. Sure enough, there was a fairly large lump on my right side. I called my mom, but she wasn’t home – I left a message, then started to pray.
I occasionally read of people being so into their prayer that they would end up face down on the floor – well, that’s what happened to me. I finally accepted the fact that yes, the chance of have testicular cancer was significant. And I gave it to God – I remember praying that it was totally out of my control. What lay ahead wasn’t going to be pleasant, but I had no options. Ignoring it wasn’t going to make it go away, and I wasn’t ready to die. But as I was lying there, I felt God’s presence – I knew that He was in charge, and knew that He wasn’t going to leave me alone. Even though I was scared to death, this was the first time I had any sense of peace since the beginning of this ordeal.
Actually, death doesn’t frighten me. If I could be assured it would be quick and painless, I wouldn’t mind if I go tomorrow. But seeing my dad go through years of treatments and eventually wasting away – I didn’t want any part of that. I remember when I would be at home, Dad often couldn’t sleep due to the chemo – I would see him downstairs in the middle of the night, head in hands. He never complained, but it was obvious he was struggling. I don’t want to go out that way.
On top of that, I have had a deep-seated fear of needles for my entire life. When I was 7 or 8, I had strep-throat several times in a two year period – and every time I ended up getting jabbed with a shot of penicillin. After that I went out of my way to avoid shots. Other than a booster before I went to college and four shots when having an ingrown toenail removed (which was one of the most painful experiences EVER), I never would let a doctor stick me for anything. The mere possibility of having blood drawn or getting a shot made me break out in a cold sweat. Having to go through that on a regular basis, as is common during chemotherapy, was my idea of hell on earth.
Twenty-Four
Things moved pretty quickly over the next 24 hours – Mom eventually called back, and I told her what was going on. She called Dr. Simmons, who agreed to see me that night. So at 10:30PM, I was in his office, showing him where I had felt the lump. He felt around for a bit (always an unpleasant experience), and said it was probably epididymitis, an infection of the testicle. It’s generally caused by sexually transmitted diseases (which obviously wasn’t my case), and isn’t uncommon among weightlifters. Considering I had been pushing myself so hard at the gym, I was relieved to hear that, and went home, assuming that was that. I just had a urologist appointment the next morning to make sure.
So I drove to the urologist’s office, who again felt around, and he too said it was probably epididymitis, but he wanted to get an ultrasound just to make sure. Fine – another annoyance, but my day was already shot and I had nothing better to do.
After a long wait at the outpatient center, I was finally taken back to the ultrasound room. As the scan seemed to go on forever, and the technician made some pretty un-encouraging noises – heavy sighing and the like – my heart dropped. I knew it wasn’t good news. Finally I got out of there and sat by the phone at the hospital, waiting for the urologist to call back with the results. When he did call, he did not have good news. He said there was a solid mass, and that it looked cancerous. He wanted me to come back to his office to discuss the situation further.
At some point my mom came into the picture – I don’t remember if she came to the hospital with me or met me there. At any rate, we left the hospital to go back to Dr. Khim’s office. He sat down to speak with us, and explained the situation. My right testicle would need to be removed, and the mass examined to determine the makeup of the tumor. The good news was that testicular cancer has a 90% (or better) cure rate. That really didn’t matter to me – I didn’t want to have to deal with the cure! At that point I wasn’t interested in what lay ahead though – i just wanted to take care of the situation at hand. Being Memorial Day Weekend, he could do the orchiectomy (removal of the testicle) the following Tuesday, or work me in late that afternoon. I was fine with waiting until Tuesday, but Mom wanted to take care of it as soon as possible. Which was probably the best thing to do, so at 3:00 I was checked into the hospital, in my lovely gown.
They rolled me into pre-op, where a very nice nurse put in the IV – either due to adrenaline or her skill, I barely felt it – a good sign! I couldn’t stop shaking due to nerves, so another nice nurse pushed some drug which calmed me down with a quickness. I was taken into the operating room, moved myself onto the table, and started to look around. I wanted to be alert for as long as possible and remember as much as I could. I looked over at the clock, saw Dr. Khim enter the room, and I was out like a light.
Big Bucks, Big Bucks – No Whammies!
I woke up in the recovery room, and thankfully I wasn’t crying, as I did when I had my tonsils removed in the second grade. The first thing the nurse said to me was “Looks like you’ve had a double whammy!” In my half-conscious state, I had a horrifying thought: “Oh no! They found cancer on both sides.” Before I could consider the possibility of being a eunuch, I passed out again. As I faded in and out of consciousness, the nurse drew some blood – I had asked them to do it while I was under anesthesia, but apparently they needed to take it again. But I was so out of it I didn’t notice at all.
Eventually I was taken to my room – the doctor had said beforehand that I would be able to leave that night, but I found out what exactly “double whammy” meant – turns out that while they were rooting around in my abdomen, they found a pretty large hernia… more than likely, that is what I felt three weeks prior after my workout. While a hernia is never fun, I’m thankful that it happened, because otherwise it might have been months before I discovered the lump on my testicle.
Anyway, when they discovered the hernia, a surgeon who just happens to deal with them was nearby, so they brought her in to fix things on that end. But the dual-nature of my surgery meant I wasn’t going anywhere that night. After a night of some painful trips to the restroom and nurses coming in at 4AM to inform me of the checkout procedure, I left for home. Mom was supposed to have a baby shower for my cousin Leigh Ann that day, but it was called off despite my protests. I felt relatively well, just weak and sore from the surgery.
The doctor told me to take it easy for the next couple of weeks, which I was more than happy to do. The stress of the previous month left me in need of some R&R, and while this wasn’t the ideal situation, I wasn’t going to complain. So I spent the next two weeks in Mom’s bed while she slept in Molly’s room. I would come to loathe that bedroom.
Tumor Markers
After a week of resting at Mom’s, I went back to the urologist for my follow-up. Dr. Khim mentioned that the tumor was indeed cancerous, but that we caught it early. There were a number of possible treatment options – chemotherapy, radiation, further surgery, or simply surveillance – the last option was definitely what I was hoping for. But more tests were necessary… i.e. more needles. Some blood was drawn, and i was sent on my way, to wait for a few days until the results came back from the lab. I also had a CT scan which thankfully came back negative…. the first good news in a while.
The next week, Dr. Khim’s office called and said my Alpha-Fetoprotein (AFP) tumor marker was elevated – it had actually gone up from 100 to 180 in the week since the operation (“normal” is 8.5 or below). Basically this meant that there was still cancer in my system, but since the CT scan was negative, it wasn’t localized in my lymph nodes yet. So I made an appointment with an oncologist.
While this wasn’t the greatest news, in a strange sort of way I wanted to do it. I didn’t like the thought of surveillance – though it’s by far the most desirable option, knowing that I would need to be constantly aware of what was going on physically, and knowing me, I would always be worrying about every slight health irregularity. Also, It seemed kind of anti-climactic to just be done with the whole situation so quickly. Cancer is supposed to be dramatic and life-altering. A quick surgery and a week of bed rest hardly seemed appropriate. What was I THINKING?????
The oncologist was Dr. Jameson, who treated my dad while he was going through chemotherapy. I didn’t know him from Adam, but Mom thought highly of him. He told me that I would need chemotherapy, and explained what was involved. I was somewhat familiar with the regimen, as I had been reading through the TCRC website, which has been an invaluable resource throughout the course of my treatment. I would take three cycles of chemotherapy, each cycle lasting four weeks. More than likely, this would wipe out the cancer completely.
So on June 16, at 8:30 AM, I stepped into Columbia Oncology to begin chemotherapy.
I’m wiped out – I’ll have to finish the story later.
On your mark…
Posted by Lane in Cancer, Health & Fitness on May 6, 2004
Well, I’ve found my next race. There is a 5K being held at Opry Mills on Sunday Morning, May 23rd. Even though I’ve barely run since my last 5K over a month ago, I will be there. May 23 will mark the one year anniversary since my cancer diagnosis, and I figure that is about as good a way as any to make a statement about my health