Hi, just wondering if anyone else has experience with PV? Particualrly at a younger age, my consultant has only had any contact with one other person under 50
I'm sorry to hear you've been diagnosed with Polycythaemia Vera but I'm glad you've joined as we have a few members who have the same diagnosis as yourself, two of which are [@Lys] and [@Daigon]. Now that I've tagged them in this post I'm sure they will reply soon to say hello and share their experiences with you.
I'm not sure how much you know about PV already but I have included some information we have about it on our website in case you want to find out more.
