January 12 2010 23:21

One Year after a Cancer Diagnosis

Today was sort of a surreal day for me. Exactly one year ago today, I was sitting in the ambulatory surgery center at Weill-Cornell Medical Center waiting for an orchiectomy. This was after a whirlwind diagnosis between Christmas and New Year’s, where I went from having a little back pain to finding out I had cancer. And exactly one year ago today, I learned that the cancer had spread and I would need additional treatment.

I’m still trying to get my head around everything that happened. While it’s obviously had a permanent impact on my life, it is also very weird to think that this all happened within the past 12 months. Maybe it was just the way I’ve been dealing with it, but it feels like the distant past to me now.

What was perhaps even more surreal, however, was the fact – exactly one year later – I spent all morning at Weill-Cornell Medical Center going through nearly the same battery of tests. This year, the CAT scan and blood tests showed nothing and my appointment with Dr. Scherr was decidedly more positive. Of course, simply spending a few hours in the hospital – especially on the anniversary of such a fateful day – brings with it a wave and range of emotions that was difficult for me to fully comprehend. I have been simultaneously angry and grateful and nervous and relieved and relaxed and terrified today.

On the whole, I feel absolutely wonderful. I’m in better shape now than I have been in years – of course, working Equinox will help with that. There are still some lingering side effects from the surgery and chemotherapy - the most notable of which is neuropathy, which basically means occasional numbness and tingling in my feet and arms, cramping in my legs, and related complications – but overall I have very little to complain about.

I’ve talked a lot in the past about how adversity figures in and how this experience has made me a stronger person – but I decided I also want to be able to say that literally. After turning 30 and beating cancer, I decided a good goal was  to beat my personal bests in weightlifting. So, consider this my public commitment - by the end of this year, I will either do a single rep of 550 lbs or do 35 reps of 225 lbs. I’ve only started lifting heavy again in recent weeks, but I think this is something I can do… and I will literally be able to say I cam out of this thing stronger.

(Cross-posted from tmarman.com)

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July 22 2009 21:02

My First Haircut and the Journey to Normalcy

The experience of the past seven months has caused me to subconsciously divide my life into my own personal eras: “B.C.” (Before Cancer) and “A.D.” (After Diagnosis). Somehow, the seven months I’ve had so far in the A.D. period seem like forever compared to the 29 years I had in the B.C. period.

At the same time, there are these little milestones and victories that suddenly take on new importance in the A.D. world. I had such a milestone today: my first haircut since before Christmas last year.

In the grand scheme of things, it’s really such an insignificant event – I’ve had several hundred haircuts in my life to this point and will hopefully have thousands more. That said, in some small but important way, it feels like a huge step in my journey back to normalcy. And normalcy feels really good right now.

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Recovery

July 19 2009 11:53

Ally needs your help to raise money for the American Cancer Society

As I mentioned recently, my sister is running the NYC Half-Marathon in part to raise money for the American Cancer Society. She has raised almost $1,100 to this point – more than the minimum to run – but would still like to reach her goal of $2,500.

The American Cancer Society is dedicated to eliminating cancer through research, education, advocacy and by providing services directly to families affected by cancer. It is also one of the most efficient and influential non-profit organizations on both a national and international scale.

I know many of you have already donated, but if you haven’t we would greatly appreciate your help. You can read Ally’s reasons for running here and – if you’re so inclined - make a donation. Any amount – even $5 or $10 – will help and your donation is of course tax deductible.

You may have also noticed that I’ve added Google ads to this site. We probably won’t make much given the relatively modest traffic here, but I will be donating all ad revenue to Ally’s run (in addition to the donation Tara and I made already).

If there are any organizations out there interested in sponsoring her race (for ad space or otherwise), please let me know and I’ll put you in touch.

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General

June 26 2009 01:27

Well, if nothing else at least I set a world record!

While the best news was finding out that I’m cancer free, I was still pretty psyched that I was able to set a world record as a result.

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June 16 2009 16:29

CANCER FREE

I just got home from my post-op follow up with Dr. Scherr where I got some really great news: I am now officially cancer-free.  They took out 43 lymph nodes total, all of which came back negative for metastatic carcinoma. I need to follow up with Dr. Scherr in 3 months for continued monitoring, but as of now I am completely done with treatment!

I also had the 54 staples removed; it was unpleasant but not terribly painful, except for the one troublemaker that they had to call in reinforcements to get out. That said, getting the good news first definitely made this process a little easier!

So, now I just need to focus on recovering from the surgery and hopefully life can get back to normal soon.

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Diagnosis | Status

June 15 2009 13:08

Support my sister as she runs for the American Cancer Society

19033.793104035.customMy sister Ally is running the NYC Half-Marathon to raise money for the American Cancer Society.

Her goal is to raise $2,500 – of which she’s raised $345 so far. Every little bit helps – so if you’re so inclined, please support her as she raises money to help fight this awful disease.

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June 14 2009 15:13

Surgery and the Hospital Stay

So, I had the RPLND surgery last Thursday. I’m home now recovering, but figured my tweets tell the story best.

  • On my way to the hospital sporting my @adaptiveblue shirt and @reprisemedia hat. Need @notches boxers (5:26 AM Jun 4th)
  • Resting comfortably - the morphine helps. Finally got a room/bed after 5 hrs waiting in recovery on the stretcher. Soooo thirsty but can’t drink yet (8:29 PM Jun 4th)
  • Fitful sleeping even with morphine and ambien. Oscillating between discomfort & pain. (2:33 AM Jun 5th)
  • Dr Scherr said surgery went well. Will have pathology report next week (2:34 AM Jun 5th)
  • According to my doctor, today's gameplan is to walk and to try to fart. If I fart I can start drinking. Go Farts! (7:30 AM Jun 5th )
  • The hospital lets you buy cable for 10$/day. They SHOULD allow you to pay more to keep you roommate from using it. I would pay anything not to listen to any more Tele-fucking-Mundo (10:12 AM Jun 8th)
  • Sad moment - they took out my epidural, so no more pain button. On the positive side this means the catheter will come out soon too (10:33 AM Jun 8th)
  • I am moving on to solid food today - and after 2 Percocets and no food for a week they expect me to set my menu for the next 3 days? WTF (8:20 AM Jun 9th)
  • Rumor has it they're letting me out tomorrow, though I'm still not entirely convinced that's a great idea. But it will be nice to get home (9:33 PM Jun 9th)
  • I have walked past the burn unit 100x during my stay here and still get very emotional reading the wall of cards to sept 11 victims (12:35 AM Jun 10th)
  • When selling you on the benefits of the epidural they don't tell you about the dark side of the pain btn: the catheter (12:47 AM Jun 10th)
  • It's kind of trippy listening to my new roommate go through and be told all the things I heard a week ago (9:50 AM Jun 10th)
  • ... Especially since I was so drugged up when I first heard it. (10:04 AM Jun 10th)
  • I felt like offering my own advice but to paraphrase Office Space, let's pretend I can't hear through the curtain (10:08 AM Jun 10th)
  • Discharged from the hospital and en route to Brooklyn with percoset in hand. Can't wait to shower and sleep in my own bed (4:41 PM Jun 10th)
  • Three words: "hooray for percoset" (7:14 PM Jun 10th)
  • After a week of sponge baths and baby wipes, it felt amazing to take a proper shower. As an added bonus, I used shampoo for the first time in 4 months (9:38 PM Jun 10th)

Each day is a little easier than the last. There’s been less “pain” per se compared to the first operation – getting in and out of bed is a little easier – it’s just a higher level of general discomfort. Each day is a little better than the last. I can even lie on my side now without too much pain.

I have a follow-up appointment with Dr. Scherr on Tuesday at which time I’ll get the pathology report and have the 54 staples removed, some of which can be seen in this photo along with the bruising on my stomach. As you can see, they literally go around the belly button. (I decided to make you click through instead of posting directly in the post for those who are a bit more squeamish. Consider yourself warned!).

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Treatment | Status

June 12 2009 07:30

Thanks for the love and support

I can’t even begin to tell you how important the love and support from friends and family has been throughout this process. I’ve tried to respond to everyone, but the outpouring of support really means a lot.

To that end, I recently got a touching email from Mike - a good friend from college and former colleague who spent the past year teaching down in Ecuador - that I felt compelled to share here.

Tim,

I want to wish you the best of luck next week, and let you know you have a good group of kids praying for you in Quito. I look forward to seeing you when I get back.

Be well,
Mike

quito

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General

May 27 2009 23:53

Post-Chemo Update

Sorry – this update is well overdue.

Finishing Chemo

As I mentioned in the previous update, I had what is hopefully my last day of chemotherapy a little more than a month ago. Chemo is a cumulative thing and it definitely caught up with me in the end. I was sick for the first time the Monday after the final cycle, and it took a full week and a half before I really started to recover. On the whole I felt pretty good after a few days, but I would sometime have periods of time where I would feel as bad as I did during the whole process. I would just hit the proverbial wall and it took about 2 full weeks before I got past that.

In any case, I feel pretty damn good right now. I started going to the gym about 2 weeks ago at full speed (though admittedly that is a bit less after 6 months of virtually no physical activity). And, perhaps most importantly, my hair is starting to grow again. My eyebrows have fully grown back in, my facial hair is growing more consistently, and I have a hairline now.

So, now what?

My latest CT scan showed virtually no reduction in the size of the lymph nodes from the previous scan. 

Basically, at this point, this can mean one of three: 1) there's scar tissue (about 45% chance), 2) there are teratomas (about 40% chance), or 3) there is still viable cancer (about 15% chance). Scar tissue is no big deal. A teratoma is basically a mutation of the cancer cells; though not malignant in and of itself, it must be removed because it can grow and cause problems including turning into late stage muscle cancers. And, obviously, viable cancer cells must be removed.  Since there was virtually no reduction in size after the last two cycles, Dr. Nanus feels it's even less likely that I still have cancer - but, unfortunately, there's no way to tell what is in there without surgery.

So, I’m going in for Retroperitoneal Lymph Node Dissection (RPLND) on June 4th. The procedure itself is pretty intensive, taking about 6 hours. As one site puts it:

In a nut shell, the RPLND involves an incision from just below your sternum to below the belly button (but they do go around it!). Your intestines and associated organs are literally lifted out of the way, nerves are identified and hopefully moved out of the way, and then the surgeons remove all the lymph nodes that were connected to the testicle containing the tumor.

The surgery is "complicated and delicate" and "few doctors do more than a couple of these surgeries a year". I am very fortunate to have a surgeon like Dr. Scherr who is one of the leading surgeons in this area and and does several of these per month. In other words, I’m in very good hands.

After surgery, I will be in the hospital for 5-7 nights. I've been told that the recovery is actually less painful than the orchiectomy since no muscle is cut; we'll see. But, because it's such a delicate procedure, there are a lot of potential complications, so they want to keep a close eye on me the first week. I will be on a liquid diet that first week - one of the side effects is "temporary paralysis" of the intestines and bowels. (ounds like fun). These lymph nodes are also apparently responsible for processing lipids, so I will be on a non-fat (or, at least, super-super-low-fat) diet for 6 weeks after the hospital stay.

I was told that if I eat fatty foods, it can cause the seals on the removed nodes to burst at which point “I will need to have a drain installed” to remove the lymphatic fluid. Suffice it to say that I don't need too much detail on what “having a drain installed” means to know that I won't be cheating on this diet.

If anyone wants to visit, I’d love to see you. I’ll be at NYPH (Weill-Cornell) on 68th and York, though I'm not sure yet what floor or room. I will try to post more details when I know them depending on how much connectivity (and coherence) I have. I'll try to let you know when I've been playing with the pain button, because that will surely be the most entertaining time to see me.

April 17 2009 07:58

My last day of chemotherapy

Well, assuming no further complications, today is my last day of chemotherapy.

IMG_0029 It couldn't have come at better time – the treatment has definitely been taking its toll, as you can see. For those of you who wanted evidence of my baldness, here you go. This week has been tough so far, but at least there is a light at the end of the tunnel. The symptoms that usually hit me at the end of the cycle started much earlier in the week. My appetite has dropped to next to nothing – I have a light breakfast in the morning and pretty much don't eat for the rest of the day. I spend most of the day sleeping -  I nap through treatment and sleep pretty much from the time I get home at 2-3pm through 6:30 the next morning.

Beyond that, I'm definitely looking forward to putting this chapter of my treatment behind me. I know there's still a big hurdle in front of me with the pending surgery, but the chemo definitely weighs on you both mentally and physically. It will be nice to actually be able think straight again, and be able to go out in public without worrying about a depleted immune system.

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Treatment | Status

April 4 2009 08:55

Third Cycle Update

I finished my third cycle last week. Again, things are getting marginally worse each cycle. My doctor put me on a little more aggressive anti-nausea regimen as we get into the later cycles – still no sickness, but my appetite was non-existent late in the treatment cycle and into the next weekend.

On the blood count front, my levels again dipped pretty low on Mon (0.7 ANC) but again bounced back later in the week (5.5 ANC). Tests from my follow-up visit this past week show the same pattern, so I can expect another dip into my last cycle – so while I still need to be careful, it's not something that will affect my treatment schedule (nor do I need I Neulasta).

As I mentioned, I also had a CT scan prior to the third cycle. According to the report, "the previously described, minimally enlarged, left periaortic lymph node appears smaller on today's exam, currently measuring 1.5 x 0.8 cm, previously measuring 2.0 x 1.1 cm. Previously described additional shotty retroperitoneal lymph nodes are unchanged. No new lymph nodes are identified in the abdomen or pelvis. No evidence of metastasis throughout the chest". 

One thing my oncologist mentioned is that the actual reduction in the cancer cells is probably larger than those numbers suggest. The CT scan only shows the size of the lymph nodes and doesn't differentiate between the type of cells present. What's likely, I'm told, is that some of the cancer cells have turned to teratomas. Teratomas are mature germ cells which can grow; they are not malignant by themselves but can turn into late-stage recurences particularly as a muscle cancer.

Ultimately, this means that the chemotherapy is working, but I will definitely need the RPLND surgery when it's all over. (There was only a very small possibility I wouldn't, but I was still holding on to that chance!). There's also a very, very small chance I may need an additional two cycles of chemo after the surgery, but given the reductions my oncologist said that's unlikely – but we won't know for sure until after the surgery.

Other than that, things are moving forward. I start my fourth and final cycle the day after Easter, and then will probably have the surgery sometime in mid-late May or early June.

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Status | Treatment

March 20 2009 16:48

Adversity

A lot of people keep telling me they're amazed at how positive I've remained through this all.  Frankly, I'm not sure what other choice there is. Yeah, my body has taken a beating over the past two months between the surgery and chemo. When I say I'm feeling good these days, that means something a lot different than it did six months ago. I can look in the mirror and see the toll it is taking.

As taxing as it has been, at no point did I feel I couldn't get through it. In the grand scheme of things, it's not that bad – and certainly not compared to the alternatives.

In that sense, I've been thinking a lot about adversity. I think my ability to deal with this comes from playing sports. Sports, like life, are full of crushing defeats, victories (both small and glorious) and a lot of hard work (the "time and effort") in between. Having participated in sports from a very young age, I've learned that when you invest yourself in a positive way, things have a tendency to work out better in the end – even if they seem to suck while you're going through it. My body felt pretty banged up towards the end of a football or wrestling season, but I eventually bounced back, just like I know I'll bounce back at the end of this.

To quote Harold & Kumar, "the universe tends to unfold as it should". That's not to say that things will always work out as you planned, but ultimately I do believe that if you invest yourself fully and positively then things will work out in a good way. (Conversely, I think if you're not fully invested, then you should stop doing whatever you're doing because it's just a waste of time.)

There are similar parallels with building a business, and one reason I find being an entrepreneur so rewarding. The road is paved with ups and downs. It's easy to get discouraged when things don't progress as smoothly as you would have liked, but I believe that if you're approaching it in the right way you will a return on that investment. Of course, those returns can manifest themselves in different ways – and it doesn't mean my business will necessarily be successful – but it does mean I will have been better off for doing it.

Adversity isn't a bad thing – I see it as necessary to personal improvement. Just as you need to push yourself when working out to see gains, sometimes you need to test your character and resolve. Adversity builds character and makes us stronger.

Personally, I welcome the opportunity. Bring it on, cancer.

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General

March 13 2009 08:56

Halftime

I finished my second cycle a week ago today. The second cycle was, as expected, a little tougher than the first, but not significantly so. I definitely found that I slept more during the treatment week. Still no real "sickness", but discomfort levels are generally higher than they were last time.

During the second week of treatment, my low white blood count and neutrophil levels rebounded very well so we opted not to take the Neulasta shot for now. My WBC went from 2.9 to 8.6 and my NE went from 0.8 to 7.3. I don't have the exact numbers from my blood work yesterday in front of me, but they were down to levels that are similar to the first cycle. In general, the counts will bottom out about 10-14 days after the cycle so we're expecting them to dip near where they were last time. So, I still need to be careful and we're obviously going to keep monitoring but the good news is that my body does seem to be bouncing back.

I am having a CT scan next week to see how the treatment is progressing and, hopefully, show a reduced mass in the lymph nodes.

I also want to thank everyone who has sent wishes, cards, books, hats, foodstuffs, etc. I owe a lot of people calls and I will get to them – but I do want everyone to know in the interim that I appreciate the support very much.

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Status | Treatment

March 3 2009 08:31

Well, I guess I couldn't call in sick

As those of you in the NY area know, we got a fair bit of snow yesterday. Roads were bad, and in general being out in Bay Ridge there's a lot of propensity to go wrong. When I take mass transit now, I was recommended to take the bus and avoid the more crowded subways.

It was one of those days in the past that I might have called in "sick" and worked from home – and all I could do was laugh at the irony that I couldn't stay home yesterday… because I was sick.

In any case, I started the second cycle yesterday. I was tired yesterday but part of that has been my sleeping schedule. The rooms are tight but the nursing staff is wonderful – Edna is taking great care of me and makes the whole process much easier. I also found the much larger and heavier Notches laptop was actually easier to work with for whatever reason in the chairs. It just sort of balances better because it's wider.

The only complication I have right now is that my neutrophil level is low (0.8 when normal ranges are 1.5 to 8.0). My overall white blood count is on the lower side but within acceptable range. Neutropenia is a common and potentially serious side effect that affects about half of chemo patients. A neutrophil is a mature white blood cell that are the real "fighters" responsible for protecting the body from disease and infection.

My medical staff felt because my overall WBC is acceptable, it was better not to delay this treatment. Instead, I will just get a shot of Neulasta next Mon which will help bring those levels up again quicker than normal. This means I need to be very careful, avoiding crowds, raw foods, kids with recent vaccinations and people with colds.

Otherwise, I feel fine and things are moving forward. After this week, I will be halfway through my chemotherapy regimen. I guess time really flies when you're having a good time.

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Status | Treatment

February 25 2009 08:36

There goes the hair

I started shedding my body hair last night, and I can only imagine that the hair on my head is not far behind. My oncologist said hair loss would begin right before the second cycle, so I figure that it really kick in over the next few days.

I'm not going to lie – even when you think you're mentally prepared for it, it kind of freaks you out when your hair comes out in clumps.

Otherwise, things are going well – I'm just trying to get physically and mentally prepared for the second cycle which begins next week. And I'm hoping to try to renew my license today, so at least I can get a picture where I have some hair.

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Status