Why is a new bone marrow biopsy necessary?
I’ve had ET caused by Jake 2 gene mutation for 10 years and have been taking standard dose hydra 500mg a day. I’m now 71 and have a new hematologist who wants a new biopsy with an ekg. There are no indicators from my last blood work that this is necessary other than my platelet count was 456 rather than the 400-425 desirable range. When I asked is this necessary her answer was it’s good to know how my bone marrow condition is. I get the feeling this is being done because insurance is paying. Any thoughts?
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Overall I agree the only caveat is you mentioned it's a new hematologist, is it a new institution, too? Often a change in institutions could make a difference...
Thanks. Much appreciated.
I have a three years old son who has a graft failure last year, and the doctors said a second transplant will be successful should I go ahead for the second transplant? I need your suggestion. Thank you
Hello @caizer. This graft failure for your little son has to leave you feeling like a deflated balloon. He’s been through (and you too!) so much already and the thought of having another stem cell transplant for him is a huge decision.
What was the condition that required him to have a transplant, if you don’t mind sharing. What are his doctors recommending, another Allogeneic transplant or an auto transplant, using his own cells?
He is sickle cell anemia and the doctors suggested another transplant and
am confused and don't know what to do.
Bone marrow biopsy was a tool used during the inquisition. Sedation is in order unless you plan to convert
Thank you everyone. I have CCUS or MDS. I am not entirely sure, but we are leaning toward CCUS.
I understand mutations and thought that a BMB (mine was two years ago) might shed some new light. One doctor suggested having one every few years. I assume you can have new mutations that may be addressed even if you are not symptomatic so that things might not get worse. I am not fond of hindsight, and my Mama always said, "Nip it in the bud." Any thoughts greatly appreciated?
This has to be a very difficult decision for you on whether to try again with the transplant or not for your little boy. I know personally how challenging it is to have a bone marrow transplant and can’t imagine trying to explain all of this to a child of three.
There are significant advances taking place in gene therapy which may offer other options in the future, but right now, a bone marrow/stem cell transplant remains the only potential cure for sickle cell anemia.
Did his doctor feel the donor cells didn’t engraft or was there a rejection of the cells? How did your little boy do the first time?
Tom!! I wish there were a laugh emoji because your comment had me, literally, laughing out loud!! I’ve had 13 bmbs and they failed to break or convert me! 😂
Me too @loribmt
And I agree, @thomhorowitz !