With Myleofibrosis, How Does A Doctor Determine Which Medicine To Choose
My doctor, a hematologist relies mainly on blood tests. She had me on Jakafi at first and I was needing a blood transfusion about once a month. She changed me to Inribic early in 2023 and I haven't need a transfusion since then. I have also had two bone morrow biopsies.
My husband is on Jakafi since July. He was dx with PMF in May. He presented with enlarged spleen and severe fatigue. Jakafi is the go to drug for these common symptoms. spleen improved immediately but they reduced doseage because he felt so bad. His spleen is still reduced at 10mg, he still battles some fatigue but not near as bad as when first diagnosed. God Bless you on your journey!
I Am ET,MF The Test Results Showed That I Have A Mutated CARL Gene. Is There Anyone Like Me Who Is Being Treated?
Has Everyone Who's Been Diagnose With An MPN Had A Bone Marrow Biopsy Done?
I Have Myelofibrosis- Diagnosed In Feb 2021. I Am Currently On Jakafi 15 Mg 2 X A Day. Previous 20mg One A Day.