It sounds very similar to the course of treatment I have thus far had. I too have had my stem cells collected but haven’t had a transplant. I’m just hoping the Revlimid will continue to keep working. I’m also hoping by the time it is no longer effective, there might be other options available besides a transplant. I’m sure giving up a job he truly loved has to be very difficult but at this point it all a matter of priorities. He needs to focus on his day to day health. I try not to look to far ahead otherwise you find yourself overthinking everything, and consequently driving yourselves crazy. Just enjoy every day you have together. There are no guarantees in this life.

I hope Revlimid proofs to be as effective long term for you as it’s been for me. What worries me is being lulled into a false sense of security though. I guess we all just have to live day to day and make the most out of each moment. Wishing you you the best Amy.

I came down with MM last May 21st, 2021. I'm in remission as of 2 months ago and had my dose reduced from 25MG every day to 15MG for the 21 day cycle. I want nothing to do with Stem Cell Transplants - I don't want to spend 2 weeks in the hospital and I expect my body and my mind to fight and win over this cancer. Time will tell.

I started with 10mg revlemid with my maintenance cycles...it worked for 4-6 months, until my blood spiked...they promptly put me on 15mg dose, and is where I'm at today...they determined that I have the lesser volatile MM, and unless something changes, I will be on this therapy for the foreseeable future...I have collected my stem cells, for a potential SCT, I only have a couple years left to use what I have collected, then age becomes a factor...but as time goes on, I would look at all possible therapies before suppressing my body for a SCT...I'm shooting for at least 20 years with this therapy, I will though, take what I get!...stay healthy! ..😊...