Yesterday I got a platelet infusion at the outpatient
clinic. I wasn’t at the threshold for
transfusion just yet, but I had a couple of bloody noses over the weekend and
my doc wanted to make sure that my platelet count got a boost to help with the
blood clotting issue. Since the
transfusion my bloody noses have gotten better.
Yay.
Last night my transplant coordinator, Callee, called &
said that she still doesn’t have the results of the high resolution tests for
whether or not Kyle is my match. She was
simply calling to let me know that she hadn’t forgotten about me and that she
was going to be out of the office today at a conference but she would check her
email throughout the day and let me know if she heard anything. She also said that she expects that we will
hear back on Wednesday. I am SO ready to
hear the news. Callee was so sweet and
told me she had really wanted to be able to tell me before or on my birthday,
but we are at the mercy of the lab. So,
we continue to wait and pray J
I got the hats that ordered online last week in the mail
today. Fun accessories and they will
keep my head warm now that I’m a baldie J
lol John will be home shortly with my
birthday dinner (since I can’t go out to dinner due to being neutropenic we
agreed to do Papa Murphy’s pizza tonight and we’ll go out and celebrate my
birthday once my oncologist gives me the “all clear”).
I had my first major side effect from all of this treatment
last night. The bone pain from the
Neupogen injections is intense! I told
John that it was worse than contractions (because there was no break between
the pain). I’ve never experienced pain
like this before (it hurt so bad that it make me shakeL). Yesterday, I tried hot baths and showers, ice
packs, and our heating pad to tough it out without having to take another
medication (I’m not anti-medication but I hate to take things if I can manage
the pain some other way). Finally last
night I took John’s advice and I called the on-call doc to ask what pain
medication I could take (given the fact that I’m taking so many other meds and
they all have the potential to interact and have to be processed through my
liver & kidneys). He gave me several
options and John, being the awesome husband that he is, went to the pharmacy
& picked up some Motrin PM for me.
Totally did the trick. Apparently
this bone pain is not particularly responsive to the regular prescription
narcotics and the doc said that Motrin would be the best thing to take
(according to a study he had read). He
was right!!
I’ve been staying on top of my Motrin doses and the bone
pain is more manageable now. I’ve only
got a few more days of injections left (hope my counts rebound and I can stop
on Thursday or Friday) and the silver lining is that the bone pain means that
the medication is working, kicking my
bone marrow into overdrive to produce new blood cells. I can certainly handle a few more days of
discomfort (now that I’ve got the Motrin) and I know that its temporary. This holds true for most of the stuff I’ve
been through recently. I keep reminding
myself that the discomfort, loss of being able to work, annoyance with having to go to the doctor 3-4
times per week, and all of my treatment is temporary. Temporary is totally worth it and totally
“do-able” even if I have to make
momentary goals for myself in order to get back to “life as usual” J
-Chellie
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