I was Chris' wife/caregiver & this is the medical blog I wrote during his treatment. Short history: dx in July 2010, no initial bone marrow involvement, did 5 rounds hyper-cvad protocol. Found out he is in relapse/refractory status with involvement in his chest, spleen, inguinal & throat lymph nodes, bone marrow, spine & brain in January 2011 when we went to MD Anderson for treatment. The two different rounds of chemo Chris got at MDA could not put him in remission; he died of leukemia/lymphoma on March 18th, 2011, an astonishing and horrific 8 months after his diagnosis.
There is a donation page for organizations here: http://chriscranecancer.blogspot.com

Wednesday, January 5, 2011

counts for today


Chris had his counts checked today and we met with his oncologist.
Here are his counts:

Platelets are still obviously low but at least they got a little higher!  His white blood cell level going down a bit isn't a surprise either, typical after having chemotherapy.
We won't meet with his oncologist here until after we return from Houston.  We will be leaving the 12th and reporting to the Leukemia clinic on the MD Anderson campus at 9 the next day.  We will stay as long as the specialist there, Dr. Thomas, needs us to.  She will recommend a treatment to his oncologist here and we will return to Austin to have treatment here.  His oncologist here, Dr. Kampe, said that a variety of things could happen.  Dr. Thomas could recommend the same course of chemo (hyper-cvad), a new course of chemo, stopping the chemo and starting radiation, or maybe even recommending a bone marrow transplant.  We simply won't know any of this until after all the tests have been run and Dr. Thomas decides the best course of action.  
Thanks to the generous donations from friends and strangers we have gotten enough money to cover the cost of a hotel room and for food/gas while we are there.  

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