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Hi, is there anyone out there who has been diagnosed with AML in the 20-30 age?
My only child was recently diagnosed with AML a few months ago but it still seems like yesterday. He was then further diagnosed with the FLT3 mutation. It has been pure **** as I am sure all you special people on this site will fully appreciate. Danny is going through his 4th chaemo in readiness for a transplant in which we hope the date is not further delayed. I saw him raw last night, for as much as he is so strong and has been amazing with dealing with this horrible cruel disease, he is starting to break. I have approached consultants and organisations and so far have been unable to find any other young male going through this.