I am Living with a Diagnosis of Myelofibrosis
I was diagnosed with myelofibrosis on October 5, 2018, at the Cleveland Clinic. I'm still trying to figure it out as I had never heard of it before. I was having blood draws every week but have now increased to every 2 weeks. I’m tracking that as I was never a medical person and everything is new. Also joined an MF support group which has been very helpful!
This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Blood-Cancer.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.
Join the conversation