• Doctor-Patient Meetings

    REGIONAL MEETINGS - BATH 2016Discussion on Ibrutinib treatment


  • Laugh4Rory

    LAUGH4RORY AT RADA Raised £8k for our WM Clinical registry


  • Meet the Doctor

    MEET THE DOCTORPatients meet the clinical experts!


  • Research

    We support UK Research in WMYou can help us to increase this!


  • Running for WMUK

    NATALIE PEIRE RAISED £4,300Natalie ran with her WMUK team in the Birmingham half marathon after her mum was diagnosed with WM


  • Slide 2

    WALDENSTRÖM PATIENTS STILL ENJOY LIFE TO THE FULLA WM DIAGNOSIS IS NEVER A SENTENCE !


    SEE OUR PATIENT TALES FOR INSPIRING EXAMPLES

We are the UK Point of Contact for patients, carers, doctors and nurses involved in the treatment of Waldenstrom’s Macroglobulinemia (WM) in the UK Read more

Roger
Salvage by Autologous Stem Cell Transplant

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Welcome to the WM community

Welcome to the WM community!  - a small,caring and unusually friendly place.  WMUK is an unique charitable partnership between Waldenström's Macroblobulinemia  patients, carers, specialist doctors and nurses.   We receive no government support, nobody is paid and we rely solely on your donations.  We have minimal running expenses and no paid staff, so all your donations go to our current projects. 

We have Facebook,Twitter, Virgin Money Donate, Justgiving and BT MyDonate pages to support you in fundraising events.

We work with you to provide information, support and events including an annual forum, regional days and educational sessions for doctors and nurses.  We lobby for the best possible treatment for this rare non-Hodgkin lymphoma throughout the UK, which affects up to 4000 people in the UK and we are dedicated to looking ahead for potential new treatments and needs of patients and their carers.  

We work closely with overseas WM organisations including the IWMF in the USA and the European WM network to share the latest information about WM.  We have doctors and patients as trustees and an active medical advisory board of the most experienced  UK WM doctors. There is an extensive WMUK Doctor Forum which has regular London meetings and you can also just elect to receive emailed news.  Just send us a message or email to join. 

WM is a rare, slow moving (indolent) blood cancer caused by genetic changes in the B cells (Lymphocytes) of the blood.  It disproportionately affects older people and men have higher rates.  It is sometimes described as LPL- a lymphoproliferative disease. It is treatable, but not yet curable - but watch this space!

Learn More...
  • 8 per million diagnosed each year
  • Roughly 400 per year in UK
  • 5 men to every 3 women