If so, any suggestions would be appreciated. I'm 75 in January so transplant does not seem to be an option. I'm the type of person who does best with what they know concerning a serious health issue. Thank you in advance for your help.
I have PV on Jakafi 20 Mg twice a day for 5 years so far so good 💪
Welcome, Laura. I'm happy you found this group...so supportive and caring. I have Post PV myelofibrosis, and I'm on JAKAFI. Some days are better than others. Exhaustion seems to come out of nowhere, but it passes.