Monday, Monday....
...So good to me...
Well, to SERRY, that is. It's her LAST MONDAY of radiation. Anybody want to raise the roof?! :) 4 more days, one more chemo (of this cycle) and then it's OVER!!! Here's what we need:
*Continued high white blood cell counts
*SOUND sleep
*Peace and rest for Serry AND the family
*More calories going in and being digested (the radiation is burning Serry's throat--so it's pretty painful to swallow "real" food)
*The effects of the current chemo to dissipate over the next few weeks.
OK, I've promised this for awhile and (now that it's past my bedtime) it's time for me to give you a little peek into the future. Here goes:
As we all know, radiation and this round of chemo ends this Thursday (YEAH BUDDY!). :) After that, Serry will need approximately 6 weeks to recover from the treatment she's received. It's pretty amazing that the things that are designed to help us also hurt us. Therefore, I think she's looking VERY MUCH forward to some recovery time. They've said that it'll take a few weeks for her to start feeling better and for some of the symptoms to dissipate. That puts her feeling better a little before Christmas--HAPPY! :)
During her recovery time, Serry will still be actively healing. She'll be making trips up north again to allow the doctors to harvest her stem cells. There are a few ways that they can do this, but, last I heard at least, they'll be hooking her up to a machine that will filter cells out of her bloodstream. I'm not exactly sure how that works, I just know that it sounds MUCH more pleasant than withdrawing bone marrow--which was another option! They will store these stem cells for use after her next rounds of chemo.
So that brings us to the chemo discussion. After her 6-ish week "vacation," probably around the first of the year, Serry will begin chemotherapy. If you remember, the chemo that she's on right now is sort of a generic chemo. It's given to many cancer patients, and is often used as a "wake-up call" for the body. Sort of a starter chemo--like an unpleasant appetizer. The chemo that she'll be getting in January is... well, intense, to say the least. We're killing cancer here, and they're going to be treating it as aggressively as possible. After she's given the chemo, she will need to have her stem cells transplanted back into her body. The chemo will have killed off her white blood cells--and the stem cells are what will make her body produce more. This process lasts about a month. Then it's Rinse and Repeat... four times. It will be a long four months... but it will only be a memory in April or May.
If you're the praying sort, please keep Serry in prayer in preparation for that time. I'm not really sure what we're going to be facing ahead... I haven't done much reading about stem cell transplants or anything--I know it's going to be hard, but---and Serr, this note is for you---Serry can do ANYTHING she sets her mind to. (You should have seen her as a kid... shimmying up trees that shouldn't hold anyone's weight, sledding on the edge of the gravel pit--she's crazy.)
Oh, and a special note just for Serry's friends at CB (did I get the acronym right? I always get it mixed up) at WSU:
You. Are. Amazing.
Seriously. Serry got your cards and gifts on Saturday night... and cherishes everything. Your hearts, your generosity, your love... Serry was in tears--she misses you so much and can't believe how much you care. THANK YOU.
That's all for tonight.
7 comments:
Ms. Serry,
This is the last week so hang in there, Girl. It sounds like you are handling everything amazingly well. I guess the thing is to take it one day at a time and before long, it will be spring. I stand in awe of you and your ability to cope. You, obviously, are well loved by all these amazing friends and family but most important by God. three more days after today.
Serry, it sounds like it's going to be a long hard trip. We got your back.
Hi Bauer! It was good to see your mom over the weekend. It is also great that you are almost past the first milestone. We will keep you in our prayers.
Serry,
You really are amazing and an inspiration to us all. I don't know much about white blood cells, but I know a little something about calories: Baskin-Robbins Ice Cream. It should be easy to swallow and it tastes oh so good. Treat yourself to something delicious.
Sheila
Serry, I hope that you are doing well these days. It sounds like your treatment had been a rough road so far. Keep you spirts up and try to get pleny of rest. I know your mom is there making sure you do just that! Today here in Texas we had another sunny day! It is hard to think of it as late fall, but the sun sure puts you in a good mood! I wish you were down here to feel the warm sun on your face and suns rays warm your bones! We are thinking of you constantly! Keep hanging in there, only three days to go! And to Sheila, great idea about the ice cream! Eat some for me Serry!!Love, Brandie
Serry, the ice cream idea is awesome. If you need someone to show you the ropes of ice cream eating, call me! I consider it a food group of it's own!
Let us know when you feel up to eating good stuff again. Bob would be happy to make you some Bobby fudge!
We love ya,
Bob and Eileen
Serry, you don't know me, but I am your mother's cousin. (something like that) We here in Ky. are praying for you. I have been following your progress. Keep up the good work and we will keep you in our prayers.
Janet
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