just wondering? traveled over from dublin last year and found it helpful
will there be a living with mpd's day 2015? - MPN Voice
will there be a living with mpd's day 2015?
hi can I ask what was usful as wasn't on the site last year still learning
HI Shelly, there are video presentations from the day on our website, this link will take you to the page, mpdvoice.org.uk/get-involve..., all the presentations were given by leading MPN experts, also on the website are the video presentations given on the day before the patient day, these presentations were given to all the healthcare professionals who attended the day mpdvoice.org.uk/get-involve... I hope you find them interesting. Maz
hiya i didnt know what to expect going. i was going for my seven year old daughter that has ET, i came away from the day feeling more positive than i have since she was diagnosed at four. There is so much going on in the world of mpd's world wide its very reassuring to hear the experts and talk to other patients and hear their stories. Was nice to see other patients that are 'living' with ET for a long time and still doing well
Hi Kentuckyrain, yes we will be having another living with MPNs day this year in November in London, I will announce details as soon as they are available. Hope you can come again. Maz
Any sign of a Cambridge forum yet?
Morning Maz!
I'd just like to say for anyone who hasn't attended a formal forum, and the patients day, how very worthwhile they are.
The consultants and haematologists are a wealth of knowledge ( obviously ! ) and happy to answer any questions you might have.
They're also a brilliant opportunity to meet up with other like minded patients and share experiences.
Louise