The end is near

Well, one more hockey game is in the books. We played the number one team in our division, which meant an 8-2 loss for our team. Personally though, I wound up being +1 for the night. I would like my Selke trophy now, please.

I wound up missing the first ten or so minutes of the game due to traffic being a complete parking lot on 2 East. It took around an hour to make the 9.8 mile journey. I was a little stressed when I got there. I wound up arriving just as the warm-up ended and wound up wearing myself out trying to get all of my gear on quickly. Idiot. Then, of course, I go out on my first shift and give 180%, which means I give 80% on my next shift, 50% on the next and so on through the rest of the game. Oy. But I did what I could to keep the puck out of our net, including flattening one of their players before he could get a breakaway or pass the puck.

And I still haven’t gotten a penalty. I blame the cancer. We now have three more games left, one of which was rescheduled to the day after my chemo, so I have two left. And no, we’re not going to make the playoffs – one of the few certainties in life…

Speaking of which, next week is my LAST TREATMENT! A few more days of feeling like crap and I’m done! My little gift for myself? I’m designing myself a “Cancer is my bitch” bumpersticker to apply to my truck. I’ve found some places that will do short sticker runs for pretty good prices. Oh yeah!

If I didn’t respect Bill Watterson so much, I’d have them make a Calvin peeing on cancer, but I do and I live in the upper class north, you know. Meh.

The Results are in…

Went to the doc yesterday for the results of my latest PET Scan and… we’re almost there. The doc who read the exam actually used the phrase “dramatic improvement!” I’ve now gone from Hodgkin’s all through my chest and lymph system to a small spot of activity in the center of my chest (where a huge mass was before). They also picked up some activity in my left pectoral area, but they’re not quite sure what is causing it, as there’s no lump to match it up with on the CT portion of the exam. Dr. Davis thinks it might just be an inflammation of some kind that’s giving us a false positive, so we’re going to keep an eye on it.

So, at this point, I’m not completely out of the woods yet. But I have two more treatments to go, so I’m definitely in a pretty good sized clearing. At this point, I think it’s safe enough to say it:

Cancer is my bitch.

Ten down, one to go…

Yesterday, my white blood cells were back up to above-normal levels, so I got to have my chemo treatment. Two more to go now!

I think my body got used to not having chemo after three weeks, ’cause it seemed to hit me harder than usual afterwards. Back to the old school tired. This morning I don’t feel too bad though.

Now it’s off for a PET scan to see just how much of the cancer’s ass we’ve kicked. Time to go drink some gross drinks and sit around for awhile. Yay.

And this afternoon, I am NOT going to forget my Neulasta!

Bad, but not horrible news

Some bad news on the chemo front – my white blood cell count was too low to get my treatment. I guess that Neulasta shot is doing something besides making me sore and tired after all. What does this mean? Well, first, it means I’m really depressed. Second, it means the treatment gets put off for a week. Unfortunately, there’s nothing I can do to make my body produce more white cells. Luckily, there’s also not much I can do to prevent it from making them either. So now it’s just a waiting game until next Thursday, then we’ll do another blood test and see where I stand. Ugh.
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Sick and Tired

Well, no hockey last night. There was hockey to be played, but I couldn’t play it. I wound up catching a cold/flu type of thing from Barb, naturally right after my last treatment. I’ve been recovering ever since. Yesterday most of the congestion and stuff was gone, but every muscle in my body was unbelievably weak. I had to sit out my first game.

On the plus side, I was going through some of the Hodgkin’s message boards the other day and discovered that I actually am rather tough and unbelievable. Possibly even badass. There were many posts where the poster would talk about how long it took them to recover from each treatment, or people who had their last treatment a month ago and are wondering when they’ll be able to walk up a flight of stairs without losing their breath.

I’m playing hockey and I still have three treatments to go.

In some ways, it makes me feel better, realizing that I really am tough when it comes to this stuff and understanding why the doctors and nurses look at me the way they do. On the other hand, when I feel like I feel now, I can’t just give in to the tired. I know that I’m stronger than this and it shouldn’t be bothering me, even though in all reality it probably should. It’s just a continuation of a neverending tug of war in my brain. Just one more way to beat myself up, I guess.

Next week, I’m back in the rink though. Just watch me.

We’re now 1-1

What a difference a pair of skates make. I went and bought some larger skates on Tuesday and that took care of 90% of my suck. These are nice and roomy and fit my feet well. Interestingly enough, the guy who sold them to me has a wife who’s 80% done with her own chemotherapy.

Does everyone have cancer? It’s getting so played out.

So I was skating much better last night (Barb said I actually looked like a hockey player of some sort) AND I even got a goal!
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The Itch is Back

Well, the itchy hands thing has come back. I went to see my doc (who wound up as one of the top doctors in the nation according to a recent US News & World Report article) and he said it’s not related to the Hodgkin’s. He said I’ve been doing so amazingly well and the nodes have shrunk so much, that there’s just no way the cancer could be doing this.
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Today Means Yesterday

There. Got that out of the way, first things first. It’s almost one in the morning on Thursday, but all of the proceeding tale happened on Wednesday. Because of that and the fact that I haven’t been to sleep yet, today is still a part of yesterday to me and will be referred to as today. Or vice versa. Go it? Good. Explain it to me tomorrow. Today. Whatever.
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I Deny the Denial

First off, does R. Kelly really have a song about hiding in a closet, or is he just playing a big prank on me? Not sure why he would, other than I like Me First & the Gimme Gimmes covering his music more than him singing it.

On to the post.

So I realized today that I’m not really sure how my mind is accepting/treating my cancer. I’ll explain.
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Around for a bit more…

So one thing we forgot about during the honeymoon planning was that I’d need to be back in Hartford the day after my treatment to get my Neulasta shot. We talked it over with the doc and nurses and decided we could get barb to give me the shot tomorrow. They called in to place the prescription and we went to pick it up. Turns out, my insurance plan has a $3000 limit on prescriptions. One Neulasta shot costs around $2700. Eeeeyikes! When they give the shot to me in the office, it’s billed differently, so it doesn’t count against my limit. Which means we have to spend the night in Hartford, or drive 2 hours to our honeymoon spot in RI, then two hours back to here, then two hours back again. Oy. We’re spending the night.
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