MDS is a bone marrow failure disorder
MDS is a blood cancer
Learn More >

Welcome to the MDS Patient Message Board Post New Thread

Welcome to the MDS Patient Message Board. We hope that you will find this to be a very valuable resource in your journey. We have recently revised the format of our forum to be much more user friendly and pleasing on the eyes. Let us know if you have any problems, or if you have additional suggestions on how we might further improve our site.

Very confused about bone marrow biopsy results – any thoughts??

Home Demo forums Patient Message Board Very confused about bone marrow biopsy results – any thoughts??

Viewing 6 posts - 1 through 6 (of 6 total)
  • Author
    Posts
  • #3821
    Sarah J.
    Member

    Hi everyone! Remember me? I’m the somewhat new, quiet girl… I need some advice if anybody has any:

    I had my second bone marrow biopsy on January 6, 2005, and just got my results the other day. The doctors said that originally I had a problem with chromosome 5 but now chromosome 5 is ok and there is a problem with chromosome 8. They also said that there are signs of fibrosis and inflammation in my bone marrow. The doctors said that they are very perplexed and want to see me in early April to go over everything with me. I am flipping out! I can’t wait until April, so I am getting a second opinion with another doctor. Is this good news, bad news, or indifferent news??

    #3822
    sarah
    Member

    Sarah, I think a second opinion is a good idea. I would get an appointment with a center of excellence.

    #3823
    Joannie
    Member

    HI Sara,

    I too would try to get to a center of excellence and get another opinion soon. April does seem to be a ways off. I personally don’t have any idea what exactly your results mean. Good luck and take care! Joan

    #3824
    Neil
    Member

    Hi Sarah,
    Have you been seeing a hematologist?
    Did a pathologist or hemopathologist interpret your BMB samples?
    Not sure why they found an abnormal chromosome 5 then changed it to chromosome 8. Would suspect there might be a lack of experience. If that is the case would certainly get to a hemo with experience and with pathologists experienced in seeing marrow of MDS patients.
    Would want to get the chromosome 8 situation clarified as soon as possible. Not in April.

    #3825
    Terri
    Member

    Sarah, Neil may be right about the lack of experience. I know that when our doctor does this for Bob he wants to send it to One lab that has the expertise with this. My insurance requires it to go somewhere else that he feels is not as capable of. Bob has had in the last year and a half 4 BMB from this doctor, each time he gets it paid somehow with this other lab, My insurance will not pay Out of network labs. I am grateful he has done this as in your case the Experience does matter.

    Wish you luck with the second opinion. Hope all goes well

    #3826
    sarah
    Member

    Experience does matter in something this serious. Hope you get that appointment soon.

Viewing 6 posts - 1 through 6 (of 6 total)

Register for an account, or login to post to our message boards. Click here.

  • You must be logged in to reply to this topic.

Login

Login

Search Forums

Review answers to commonly asked questions or get answers to your questions from an MDS expert