Friday, March 18, 2016
So how is Derek? I am frequently asked that question, and I’m
not sure how to answer. He is NOT ok,
but he is doing ok for not being ok. The steroids, which ended early last week,
produced a good appetite, but his energy level has been very low. He developed
painful mouth sores that made it difficult to eat. Fortunately those are gone
now, but he has nerve pain in his legs and sometimes
Sunday, March 6, 2016
On Friday, we started a protocol that hopefully will start
to bring the lymphoma under control. Derek had to have intrathecal chemo under
light sedation so he couldn’t eat before the procedure which was at 2 p.m. Even
though he has been NPO at least 50 times before and two other times already
this week, it does not get easier, especially
Thursday, March 3, 2016
The results are mostly in, and now we know. Derek has T-cell lymphoblastic lymphoma. Good news is it is not in his central nervous system, and initial testing indicates it is not in his bone marrow either. The donor graft from his stem cell transplant is doing its job as far as it can reach. Problem is that it
Monday, February 29, 2016
The raucous mob outside the door make it difficult to sleep.
In the darkness, I can see their
threatening faces pressed against the window and hear their incessant banging on the
door, clamoring for admittance. I know their names. We've met before.
Racing Heart. Anxiety.
Friday, February 26, 2016
Today I had to do the hardest thing I have ever had to do. I
had to tell my nine-year-old son that his cancer is back.
This afternoon my phone rang. The call display said “City of Hope.” “It’s
either someone calling to check on Derek after his surgery yesterday, or it is
someone with news,” I thought. When I heard the urgent voice on
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