Just trying to catch up on the forum after being laid low with a virus, at least that's what I think it was. Made me realise what a mine of information this forum is and how truly helpful it is for us with this uncommon blood disorder.
Merry Christmas to everyone connected with this incredible forum and lets hope we all have a great 2017. Regards Sue xx
I couldn't agree more Sue ! Being a newbie to this rare condition PC JAK2 + I have found MPN Voice a tremendous help and support. Everyone is so caring and only too willing to offer advice, share their experiences and above all totally understand .
May I take this opportunity to wish you and everyone a Very Merry Christmas and a Happy and healthy New Year!
Dianne x
Same to you and everyone on the forum 😄👍🎄🎁🍾
Hello Sue, hope you are feeling much better now, merry Christmas to you. Maz x
Many thanks all, I may be reporting on my findings regarding erythromelalgia which I believe I may be suffering from (my own diagnosis at this stage), but I will see what the Haemo or specialist nurse has to say after my next hospital visit in January.
I`ve just managed to get tickets for the Strictly Tour in January so I may have to come down to earth after that visit. HO HO HO
Frustrated 
MPN with ME / CFS diagnosis?
Recently diagnosed with PV
Newcaslte Patient Forum?
MPD London Forum
