Friday, September 28, 2007

Day 50

Well, I'm now 1/2 way through the 100 critical days, and I'm feeling pretty good today. I've had a couple rough days this week with nausea and fatigue, but I'm working on strategies to hopefully improve both. The best strategy so far? Taking my pills with chocolate milk! The thick kind, it just takes everything down with it. And who's complaining about a giant glass of chocolate in the morning? As far as medically, I'm doing great. They think they found a little bit of graph vs host on the side of my mouth, but it's nothing they are going to treat yet, since it's not bothering me, and a little bit of graph vs host is good since it indicates graph vs leukemia. And I lost some of my eyebrows (did I already tell you that?), I'm a little upset about that, but if you look at my head in the right light there is a little bit of hair growing in!

Wednesday, September 19, 2007

Choose your own Adventure!


I know I have been terrible at editing the blog, and I apologize. But I do blame fatigue and nausea for that which has been plaguing me on and off since I've gotten out of the hospital. But otherwise things are going very well, every doctors visit I pass with flying colors and I'm feeling good.

To recap the last couple of weeks, I thought I would make it a "Choose your own Adventure" so you too can enjoy the things that I do in your own way!! Here it goes:

Morning begins between 9:30 and 10:30 with rolling out of bed, and heading downstairs for pills and breakfast.

You may either:
1) Choke on a pill (specifically acyclveir for viral protection) and promptly refund your breakfast.
or
2) Manage to keep down everything and continue with your day.

If you choose #1 you then go back upstairs to lay down, settle your stomach and nap.
If you chose #2 you have the choice:
a)Go back upstairs to lay down, settle your stomach and nap.
or
b)Workout with mom. We have been doing some weightlifting and working our abs, nothing too strenuous since my stamina for these things is very small.

No matter which you choose it eventually becomes lunchtime and there is another dose of pills, but this time much fewer and it's typically not a problem.
After lunch you usually go back upstairs to lay down, settle your stomach and nap (especially if you chose option b). Then, once you get up, the whole family takes an outing! We've been to Red Butte Garden, liberty part, the international peace gardens, driven Big Cottonwood canyon over to Park City, and Rei! Don't forget to wear your mask and stay away from any sick people and crowds.

Now, depending on the time, you either nap again, or go straight into dinner, in which case you may once again choose option #1 or option #2. If you choose 1 you go up to lay down, and let things settle. If you choose 2 you hang out with your folks until Dad has to return to their apartment to take care of the cat, which is too bad for us ladies, but we get by with the big screen tv (thanks Joe!) and cards until bedtime.

Now bedtime is the last round of pills and again the stickler pills are in that group, so you once again can choose to refund or not. At this point either choice results in the same laying down for sleep, unfortunately your dinner has had a lot more time to digest. Then, lights out and do it again tomorrow!

I apologize if this has been a little too graphic for some, but I'm just trying to keep it real ;)
However things are not as mundane as it sounds, in fact, Roni is coming over tonight to make me dinner, and Miriah is staying the night to take care of me. Liz and Roni did similar things for me last week, giving my mom a chance to sleep in her own bed and giving me a little social interaction.

So, that's your adventure, I hope you liked it. I will try to start posting more regularly!

Thursday, September 6, 2007

One Week Later

So far, Kristi's doing very well. She's eating, walking, and riding her bike. These are the main things the Docs want her doing now, that and taking HANDFULS of pills four times a day. Though she is out of the hospital, she is watched closely by her parents. For the next 70 or so days (since we are getting close to day 30 already) she's got very restricted exposure rules. She can go out of the house with a mask, but she definitely can't go to any movie theaters or things like that, this includes work/school for now.

At her first checkup on Tuesday, she had a Hematocrit of 34, which is the highest it has been since she found out in April! That's a natural 34 of course, she made it herself. It's still low, but considering how quickly it came up to this level, I am sure it will be normal very soon. So far there aren't any signs of Graft versus Host, GVHD, which is the main concern for the +100 days post transplant. She does have some elevated liver function, which could be an early sign. They are watching this closely. Kristi will be watching for any sudden rashes, which are the most common early symptoms of GVHD.

So far, Kristi is a BMT super star, that's what the docs keep saying anyway.