
Q&A with Janet – Why the WM Buddy Service really matters.
When Janet was diagnosed with Waldenstrom’s macroglobulinaemia in 2020, she felt isolated and overwhelmed. Now, as part of WMUK’s Buddy
News, updates, research & information about WMUK’s work around Waldenstrom’s Macroglobulinaemia.
When Janet was diagnosed with Waldenstrom’s macroglobulinaemia in 2020, she felt isolated and overwhelmed. Now, as part of WMUK’s Buddy
The UK government released new details outlining the next phase of its 10-Year Health Plan.
From 1st July 2025, the Rory Morrison Registry is closing. The next chapter puts ensures the WM community shapes the
Sign up to hear about the latest Waldenstrom’s macroglobulinaemia news and WMUK’s work including research updates, on-line events, fundraising and other opportunities to get involved.
“I’m so pleased to have an opportunity to support my husband and the wider WM community.” – Catherine Ferris, London
We’re excited to launch the Big WM Survey – a European-wide survey specifically aimed at WM patients, families, friends and
You may already know Alison McKinney, who set up our Support Line and staffed it for 18 months. This year,
WMUK speaking at the British Society of Haematology Conference about Active Monitoring
WMUK’s Active Monitoring Checklist Project is a Key Step to a Standard Care Pathway for Waldenstrom’s macroglobulinaemia care
We are really sad to hear of Louis Walsh’s Macroglobulinaemia diagnosis, as announced on Celebrity Big Brother.
Answers from the experts from your questions and concerns raised at Patient Summit in October 2023.
We’re delighted to announce that Charles Lilley has agreed to take on the role of WMUK’s new Chair of Trustees.
This Christmas, the WM community has come together to raise a HUGE £63,000 (including Gift Aid). When we first launched
Here at WMUK we’re constantly striving to improve care and find new treatments for WM. This Christmas we have an