Swab4Bevin

Monday, January 21, 2008

Day 6

I'm trying to keep a good recollection of everything that's going on by blogging. I don't remember much from the first time I was diagnosesd, and now that I try and think back, I wish I did. Some attribute that to "chemobrain." It usually means when chemo treatments effect the memory.

So I've started a few rounds today with a drug called vincristine and another one they nickname the peg. They went fairly well, although this is the first couple days. I should feel more of the effects this week. I had visitors this weekend, b/c it's probably the last time I'm going to have them for several weeks now. My cousins drove down from albany on Friday morning, then a bunch of friends throughout the weekend. All in all, I feel energized. It's weird, but I'm pushing myself to do laps around the hospital and not staying in bed.

Saturday, January 19, 2008

You've Re-lapsed

Those are some pretty ugly words. And so far, I've had to hear them twice in the last 6 months.
I found out on Wed. during a routine follow up that the doctors had discovered blasts within my blood. This hit me pretty hard, I think a little harder than the first time back in September. But it was imminent that the disease was going to find it's way back. I was off the juice for too long. The last chemo dose I received in the hospital was the first week of Oct. Since then, the only reason for my long hospital stay was due to infections and fungal pneumonia that was pretty persistent. That delayed my recovery time and the time for them to begin the next phase. So in my opinion, I was in remission for four months on what's considered an inadequate amount of chemo. I'll take it. I just need to be more cautious this round. I need to do whatever I can to try and keep my hospital time limited. The good thing is I've brought my weight and strength back up to a normal state. Thanks to all my workout sessions at the gym with Jay. And of course mom's cooking, who by the way, fed me like I was a 250lbs man. I was able to spend Thanksgiving at home, Christmas with the family and even celebrate the new year with a couple of close friends. So I feel good again. I know it's bound to get worse, even by tomorrow, but I've shed most of my worries. Now, it's battle time once again. There has not been one time throughout this whole process that I've felt God has left me. B/c if he left me, I wouldn't still be here. And I know he's watching and listening. I know he hasn't forgotten.

Monday, November 26, 2007

i'll take a shot at this

i don't blog. i don't even really write that well. but i guess with all of you out there who have been pulling for me, i'll do what i can to keep you posted on my progress. so after 53 days of being in the hospital, i'm finally out. i can't tell you how good it is to be home. i truly feel like my recovery has progressed rapidly being here. although i have to return to the hospital 3 times a week, i'm just glad i come back to my bed in my house.

this cycle was a lot better than the first time i had to go through it. although the chemo doses were larger and more aggressive, my body was able to respond better in strength. Maybe that LA fitness membership really paid off. I was able to walk out of the hospital instead of getting wheeled out like last time. It was a great feeling.

alot of drives have been going on these past few months. it's amazing how our community can come together if it has something to work for. Amazingly, you all have been working for me and everyone else in need of a match. It's almost incomprehensible considering I don't know many of you. but i do thank all of you for your work and effort. i have no doubt it will pay off.

i guess that's all for now. back to my xbox(thanks sand)!!

Wednesday, October 17, 2007

love you bro

Just testing out your new blog man. Making sure all is well!!!! holla if you need anything man!!!!

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