Hi @Samuelle and a big welcome to the forum.
I can imagine all of that has come as a huge shock and understandably brings with it a lot of questions and concerns.
I hope others will be able to share their experiences with you. In the meantime I have shared some links to conversations around Myelodysplastic syndrome (MDS) which are on the forum.
Awaiting or considering or had a stem cell transplant, a place to share here
MDS diagnosis at 45 with no symptoms[Being diagnosed with Myelodysplastic syndrome (MDS)]
Remember the support line is there to if you want to talk through anything.
How to contact Blood Cancer UK | Blood Cancer UK.
Sorry if that’s information overload. I just thought there might be bits from each that might help.
Take care
Nichola