Primary Myelofibrosis: Continue watch & wait? 2nd opinion?
Does anyone have PMF? I was diagnosed in July and still need to learn more about what is best for me. I’m a 67 yo female and at last visit 2 mos ago I was not experiencing major symptoms. Occasional night sweats, slightly enlarged spleen, constant fatigue. Should I go to get advice from Mayo Clinic or keep doing the watch and wait? No meds right now.. Thanks