Connect
← Return to Want to talk about Multiple Myeloma: Anyone else?
Discussion
Want to talk about Multiple Myeloma: Anyone else?
Blood Cancers & Disorders | Last Active: 4 days ago | Replies (414)Comment receiving replies
I am in remission from AML. ☺️ Coming up on 3 years post allogenic transplant. (An unrelated donor). My doctor said that AML seldom relapses past 22 months with a successful transplant and I’m at 33 so we’re all pretty optimistic.
That’s why I’m so honored to be able to help and offer encouragement to anyone else who might be facing a blood cancer and a stem cell transplant. Every day is a gift and it’s worth fighting for. So hang in there! I’ll be with here for you every step of the way.
May I ask you a little favor? I don’t want to miss your messages to me, so when you respond to one of my replies, please tap the reply button right under my posting then I’ll get a notice directly. Or, you can simply type @loribmt in any message and I’ll get a message. That works for anyone you want to reply to in their message.
Again, I’m so happy that your new medication will arrive tomorrow! Hope it a bottle, right? 🙂
Replies to "I am in remission from AML. ☺️ Coming up on 3 years post allogenic transplant. (An..."
Sorry thought I had done that but must have typed in the one below!!!
Well we did the injection so guess that is ever day now. I have a bit more pinchable skin than you so seemed to go okay although did sting a bit. Certainly better than having a DVT and/or PE!!! Halfway through my first Revlimid cycle so guess will know in early April although will be afraid to look at the results!!! I am such a wimp! Thanks for your encouragement. All the posts are so helpful in understanding how to get the right care and help oneself!!!
Connect
Thanks so much. I hope I can get back to remission. I need to focus on that but always find my mind trying to go back and change things! Thinking having the Revlimid will help if it works quickly. That sounds wonderful but I worry I will not be able to have a transplant. My local provider said I was in remission but not a candidate for it. Mayo said I could but the longer it takes to get to remission the harder it will be. My sister warned me it would not be easy because of the chemo and I know it does not always result in remission but I sure want that chance. I worry that the damage I now have plus the second round of chemo will add to making it harder. It was 5 months to get to remission last year. Worry it will take way longer now.