Once again it’s been a while since I’ve posted, but I’m busy/tired!
Cliff’s “evil” B treatment wasn’t so evil. The new group of
nausea meds the doctor gave him must have done the trick. It was a big relief
not to experience what we did with his first B treatment…that was awful! He will have his 5th chemo treatment
next Monday. We’ve decided not to have
any expectations when we go in for treatments because you never know how his
body is going to react.
Overall he has been doing well since his last chemo. The
main thing is that he’s tired. Every time he leaves the hospital he has a new
chemo symptom. This time it’s a rash on his bald head. He had a platelet
transfusion last Friday and he’ll get a blood transfusion tomorrow. After the
blood transfusion his energy level will increase. It’s always something so we
just go with the flow!
September is Leukemia/Lymphoma awareness month! The Leukemia
and Lymphoma Society is a great resource if you want to learn more about blood
cancers or if you would like to donate towards research. This is an
organization that Cliff and I will heavily be involved with after the New Year.
Click here to Donate Now!
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