Hi all, only the last two questions are relevant. I too had a bone marrow biopsy and was told my bone marrow was dry so there was no fluid to draw for testing. I was still diagnosed and started on weekly injections. The alternative is stem cell transplant but I don't want to put myself through that, according to what was described to me by the expert.
From what the inquirer described about their daughter, her doctor must already suspect the cause and wanted to verify. Need to discuss with him/her.
Not a pleasant state of affairs. Prayers for restoration.

By the way, I just received information about sleep from Mayo, while I have been waiting for over a year to hear back on consultation for my myelofibrosis condition.
Any help?