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Does Anyone Take Jakafi For Polycythemia Vera?
I just started taking it a few months ago, I used to take Hydroxyrea
I've been taking Jakavi since April 2022. I started with 20mg/day and I'm currently on 40mg/day. I have no side effects.
I’ve been taking Jakifi for two years for Myelofibrosis and GVHD. I have no side effects and it keeps the goonies at bay.
Besremi has been working for me.
I am fortunate to find this PV problem early. Has anyone been on Besremi?? Sure would like to know about this if so. It is very expensive and my co p is so very high.
What Is After Jakavi In Myelofibrosis???
Does Anyone Else Get Itchy Skin Through The Day
What Are People Paying For Jakafi
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