Hi Partick,
A BMB is normally done at diagnosis to confirm that you have CML and to have
a benchmark of what your marrow looks like. What test did he do to confirm
that you had CML.
How often are you being tested. I was tested every 3 months by BMB for about
5 years and then switched to PCR testi
I was never given a BMB unless I developed a problem with my blood.
My onc now at Moffitt tells me, after doing 2 BMBs, that I won't have to do
another unless something changes in my blood work.
In a message dated 4/14/2010 9:56:30 A.M. Pacific Daylight Time,
lblaine...@comcast.net writes:
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10 10:50 AM
Subject: [CMLHope] BMB's - still necessary or "the way we have always done
it"?
Just wondering. Am I the only one here who's never had a BMB?
About a year into my little journey my onc mentioned one. But when I asked
what we would learn from a BMB that
\
carolyn
- Original Message -
From: patrickemailguard-g...@yahoo.com
To: cmlhope@googlegroups.com
Sent: Wednesday, April 14, 2010 10:50 AM
Subject: [CMLHope] BMB's - still necessary or "the way we have always done
it"?
Just wondering. Am I the only one h
com
Sent: Wednesday, April 14, 2010 10:50:47 AM GMT -06:00 US/Canada Central
Subject: [CMLHope] BMB's - still necessary or "the way we have always done it"?
Just wondering. Am I the only one here who's never had a BMB?
About a year into my little journey my onc mentioned on
Just wondering. Am I the only one here who's never had a BMB?
About a year into my little journey my onc mentioned one. But when I asked what
we would learn from a BMB that would alter my course of treatment he didn't
really have an answer. (My CBC numbers all jumped to the normal range within 2
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