My mind has been racing ever since I received the news that I have been
matched to provide a bone marrow donation. While I am excited to be able
to make a concrete difference, I have to admit that I am now becoming
nervous. While I worry about the side effects of the medication, most of
my fretting is focused on the recipient. I want this transplant to be
successful. I know it is illogical but I can't help but feel responsible
if the donated marrow does not work.
Yesterday I met with a
donation coordinator and the physician who will oversee my case when I
passed the physical. The green light was given and I will begin the
daily injections on Monday with the harvesting of the cells scheduled
for Friday afternoon. Until then, I am going to do my best to produce
the strongest cells possible!
Robby has been hearing bits and
pieces of our conversations about the donation, and we knew that we
needed to talk with him. I don't want him to be scared by the side
effects that I could experience next week, but it is important that he
understand why I am sick. Scott and I huddled and came up with a game
plan on how to explain everything to Robby. Last night after dinner we
sat Robby down and we began our well-rehearsed speech. I stressed the
importance of helping others even if you don't know them. Scott took
the lead in explaining the process of the donation. We both tried to
convey that I might not feel well for the next few weeks, but that I'll
be better soon and that it is important to help somebody else even if it
isn't convenient.
After ten minutes of thoroughly saturating
Robby with information, we ended our conversation by asking if he had
any question. "Yes Momom, I have one question. Can I go play with my
Legos now?" We either did a great job explaining bone marrow donation or
we overwhelmed him with too much information. I lean towards our being
over-zealous. Again.
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