← Return to Myelodysplastic syndromes (MDS): When do you need to start treatment?

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@loribmt

Hi @raetp. Oh golly, this isn’t news anyone expected to see, especially your brother on his birthday! I remember that just talked about him having had HL a number of years ago with an autologous (own cells) stem cell transplant for treatment and he’d been doing so well. I’m so sorry to hear about this little setback for him.

As you mentioned there are different classifications and staging for MDS so we’ll wait until your brother knows more about his diagnosis. But try not to despair, there are treatments for MDS. The ultimate and only potential cure is a stem cell transplant using donor cells. It can be very successful. In fact, @katgob very recently had a transplant for MDS. I had one 5 years ago at the age of 65, for AML, MDS’s aggressive and nasty step sister. I’m super healthy and feel as though nothing ever happened.
So please encourage your brother and family to stay positive! We have a great support group with members who have MDS and we’re all here to offer encouragement and hope. Is he still being seen at Mayo-Rochester?

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Replies to "Hi @raetp. Oh golly, this isn’t news anyone expected to see, especially your brother on his..."

Oh yes! He still goes to Mayo. He lives in a suburb of Mpls, so Mayo is where he goes for his annual checkups. He is open to a donor stem cell transplant if it comes to that. We are just waiting right now. I will pass on to him this other person’s success with it. There is only my brother, his wife, and our 92 year-old father now. We’re not telling dad yet as he’s on his decline now and don’t want to upset him. But the three of us will work through this. Thank you for you support. 😃