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!

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