Are you a haematology patient or carer? Your voice matters! Attend the HPCC (Haematology Patient and Carers Congress) on 10th May 2024 in London to connect with peers, gain knowledge and be part of the movement to enhance support and awareness for haematological conditions. We’re excited to announce that we have a stand at the…
Saturday 8 June 2024, 10.00 am – 4.30 pm (arrival/registration from 10 am with tea/coffee/pastries) Venue Ashling Hotel Parkgate Street Dublin 8 DO8 P38N Ireland THIS IS AN IN-PERSON FORUM NOT VIRTUAL/ONLINE You are welcome to attend this forum regardless of which hospital you attend, or where you live in Ireland or the UK, if…
Saturday 11 May 2024, 10 am – 4.30 pm (arrival/registration from 10 am with complimentary refreshments) Venue The Gasworks Hotel 3 Cromac Place Belfast BT7 2JB THIS IS AN IN-PERSON FORUM NOT VIRTUAL/ONLINE You are welcome to attend this forum regardless of where you live or which hospital you attend, if you are willing to…
Friday 20 September 2024, 1 – 5 pm (arrival/registration from 1 pm with complimentary buffet lunch and refreshments) Venue The Liner Hotel Lord Nelson Street Liverpool L3 5QB THIS IS AN IN-PERSON FORUM NOT VIRTUAL/ONLINE You are welcome to attend this forum regardless of where you live or which hospital you attend, if you are…
Wednesday 9 October 2024, 1 pm – 5 pm (arrival/registration from 1 pm with complimentary buffet lunch) Venue The Royal Station Hotel Neville Street Newcastle-upon-Tyne NE1 5DH THIS IS AN IN-PERSON FORUM NOT VIRTUAL/ONLINE You are welcome to attend this forum regardless of where you live or which hospital you attend, if you are willing…
Tuesday 5 November 2024, 1 – 5 pm (arrival/registration from 1pm with complimentary buffet lunch) Venue Thackray Museum of Medicine 141 Beckett Street Leeds LS9 7LN THIS IS AN IN-PERSON FORUM NOT VIRTUAL/ONLINE You are welcome to attend this forum regardless of where you live or which hospital you attend, if you are willing to…
As a young person living with an MPN I hope that my story will provide comfort to other young people with MPNs to know that they are not alone and there is support out there for them. MPN Voice is very close to my heart as I was diagnosed with Essential Thrombocythemia in September…
“My Mum is my inspiration. I feel helpless watching her struggle with her condition and realised fundraising was my way of supporting the vital research required to find potential cures for her and others like her”. My name is Heidi Rose. I am 31 years old and so far I have raised more than £6,000…
“My wife’s illness inspired me to become a fundraiser myself, it is not something I have ever done before, but I would definitely do it again.” My wife Annette was diagnosed with Polycythaemia Vera, more than fifteen years ago so I was keen to support the charity and the work they do to make…
Researchers at the University of Oxford are working on a project that could make huge improvements to the diagnosis of myeloproliferative neoplasms (MPNs). Using AI, the research could lead to people getting an accurate diagnosis sooner and could mean that changes in bone marrow are picked up earlier, hopefully this will mean earlier access to…