Anyone else with Secondary MDS?

HI

It appears I have devloped Secondary MDS as a result of the chemo and radiotherapy treatment for Triple Negative Breast Cancer two years ago. I wonder if anyone else is in the same boat?

Thank you

  • Hello Chasco and welcome to Cancer Chat.

    I’m sorry to hear it appears you developed secondary MDS as a result of your treatment for triple negative breast cancer two years ago and I do hope you will get a chance to meet and chat with some of our members who will be able to relate to what you are going through at the moment.

    I remember that Lucie, another moderator, mentioned in a reply to [@Athene]‍  that we had a few threads on MDS here and that you can search for them via the search function on our forum.

    Also, we have some information on myelodysplatic syndromes on our website and you can read more about it here.

    I hope this helps, Chasco.

    Best wishes,

    Renata, Cancer Chat Moderator

  • Hi chasco, Sorry to hear the above, sucks doesn't it. I have recently been told I have secondary mds, two years into my treatment for leukaemia.