Happy New Year to all 🎉

Just wanted to say thank you to all for your support in 2023. It really helps hearing from people with MPNs and those, like me, with with Polycythaemia vera (PV).

Quick update from me … I’ve just had my 7th Peginterferon 2a/45 injection today. My consultant wanted to increase dose after 3rd but due to side effects, agreed to wait. Happy to say my side effects have significantly improved. Blood results tomorrow so :crossed_fingers:

I hope 2024 is a good year for all :two_hearts:

Thank you again for all your support and especially those who volunteer and support us all. Happy New Year :tada: