I was diagnosed with CMML Leukemia in 2016 and see a consultant every 3 months or so. At the moment I do not have any treatment and would like info from anyone who has similar problem
Welcome to the forum Squashboy although I'm sorry about your diagnosis.
I know you're wanting to hear from others so I just wanted to put you in touch with [@francisV]. They also have this type of cancer and joined in September last year hoping to connect with others so now I've tagged them in this post they'll hopefully be along soon to say hello and share their experiences with you.
I know you've had this since 2016 but I thought I would still share the information we have about this on our website in case you wanted to have a look. The Bloodwise website is also full of useful information about your diagnosis, and with a helpline you can call, you may find them to be helpful at this time as well.
