Polycythaemia Vera - has anyone been on Ruxolitinib?

I’ve just been diagnosed with polycythaemia Vera. Is anyone on Ruxolitinib and if so how are your side effects. Thanks 

  • Hello Irene70

    I'm sorry to hear that you've recently been diagnosed with polycythemia vera. I hope that you've been feeling well supported by the health professionals involved in your care and that they have been able to answer any questions you might have. 

    There are a few members who have recently mentioned being on Ruxolitinib. A post was shared by  who shared some of the side effects she was dealing with. And member  mentions in their post that they are taking ruxolitinib as part of their PV treatment. Hopefully you'll be able to connect with some members who have experience with this type of treatment and can share their stories with you. 

    In the meantime, if you'd like to talk things through with one of our team of nurses, you're most welcome to give them a call. I know they will be happy to listen and offer any advice, information, and support they can. They're available Monday to Friday, 9am to 5pm on 0808 800 4040. 

    I hope this helps and that any side effects you've been experiencing settle soon. 

    Best wishes, 
    Jenn
    Cancer Chat moderator 

  • Thank you so much for reaching out I’ve actually moved on from PV to MF which is myleofribrios so a bit hard to deal with I will go online and see if anyone else has this MF and see how they’re dealing with the horrific side effects of this cancer treatment Ruxolitinib