Christmas, less posts.
Hello Pearl, I agree, I like the format of this site too. Maybe the holidays keep caregivers and patients from posting.
I don't keep a diary, or a notebook for my illness. This site is how I know what I went through when I am asked at the hospital. The doctors/ transplant teams/ eye doctors etc asks When did it (itchy, inflamation, pain etc) start? I would look through my mails here, and pinpoint when it started.
Doesn't answer your question, but shows how helpful this site is for me.
Meri
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Female born 1965, diagnosed MDS RAEB1 in August 2016, watch and wait for 9 months. Sibling match - Stem cell transplant in 2017.
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