← Return to Want to talk about Multiple Myeloma: Anyone else?

Discussion
Comment receiving replies
@auntieoakley

@callie28 , @judithc I hope to give you a little information and/or encouragement with my husbands story.
He was diagnosed in spring of 2010, the first transplant at Mayo Rochester left him with a little residual disease. So they gave his body a few more months to recover and as the myeloma reared up, he went on a second induction therapy of 4 months, and back to transplant. By this time he was 70 but overall still in pretty good shape. This transplant was much harder on him, although the first wasn’t really easy. Again the Mayo team were rock stars in knowing what to expect and handling it.
This time he got a complete response, revlomid maintenance was recommended and he took that for two years.
He has had a few years at a time completely treatment free, and plenty of months of treatment that weren’t really easy, but not horrible. He will soon reach 13 years with myeloma, I believe this might have been an easier time had he been diagnosed earlier. He had bone lesions in virtually every bone when diagnosed. I believe his Mayo team and our most awesome Mayo trained doctor locally, have helped give us the gift of the last 13 years together.
If you have any questions for me, please feel free to tag me.
@judithc where do think you might be looking to have transplant?

Jump to this post


Replies to "@callie28 , @judithc I hope to give you a little information and/or encouragement with my husbands..."

Thank you for replying. It sounds like they have him on a good treatment plan.
If I have it done, I’ll have performed at mayo in phoenix.

On the same path with my husband. Diagnosed in November and started induction treatment in Dec. He will start his 4th cycle of induction therapy tomorrow. We live in Sacramento and plan to have an outpatient transplant at UCD. Has anyone else gone the outpatient route? Nervous about having him come home.