Has Anybody Ever Been Through A Bone Marrow Transplant? How Was Your Experience? How Was Your Mental Status?
I just reread the question and I see you were asking about a transplant. I have not had one but I was told last year I needed one. A lot has transpired since then and now I’m not even sure if I’m still a candidate or if I really want to go through the process. If you want to hear others experiences, there is a Facebook group called Myelofibrosis Private Support group that you can sign up for.
No he’s considering a bone marrow transplant.
I’ve had five BMB’s, the first being in 2008 when I was diagnosed with ET Jak 2. It was done in the doctors office, was over quickly, and I was able to drive home on my own. The next four were done in the hospital starting in 2019. I was lightly sedated, but my bones had become more fibrotic overtime and it was not so easy. But I’m glad I had them because they give so much more information than a blood test.
Great attitude
Positivity helps, surely
Oh sorry not transplant just biopsy 🤦♀️
Has Everyone Who's Been Diagnose With An MPN Had A Bone Marrow Biopsy Done?
I'm Wondering If It's Prudent To Wait To Do A Transplant. I Would Prefer To Take Advantage Of Advancements As They Come. I'm 67.
Anyone Here That Has Had Or Is Having A Bone Marrow Transplant?
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