This a rare blood cancer, does anyone relate to it in some way or another, I feel lost as there is so little information really?
This a rare blood cancer, does anyone relate to it in some way or another, I feel lost as there is so little information really?
Hi Evie I was diagnosed with CMML March 2021
Like you I don't know anyone with similar.
Also feel a bit lost.
I'm on a watch and wait program.
When I'm researching info keep reading it's a rare form of Leukemia
Hope your feeling well in yourself.
Hi Evie I was diagnosed with CMML March 2021
Like you I don't know anyone with similar.
Also feel a bit lost.
I'm on a watch and wait program.
When I'm researching info keep reading it's a rare form of Leukemia
Hope your feeling well in yourself.
Hi Evie et al I have just been diagnosed with CMML/2 and am waiting to see a consultant ( this Thursday) to find out what treatment I will be on. I have been told my myeloma is back in remission thankfully a condition I was diagnosed with in 2007. I have looked at the treatments for cmml and like you there isn’t too much information about it although what i have read is pretty scary. By the way I am 70 this year so stem cell transplant seems out of the question for me.
Regards to all Nick
Hi Nick
How are you getting on with your CMML diagnosis?
Hope your ok .
My husband just been diagnosed with this. Can you give me some insight into what to expect. Not much information on it. Hope you are well.