
WM Patient Priorities Shared at Major Haematology Conference
WMUK shared patient priorities on treatment at the world’s largest haematology conference, ensuring the voices of people living with WM
News, updates, research & information about WMUK’s work around Waldenstrom’s Macroglobulinaemia.

WMUK shared patient priorities on treatment at the world’s largest haematology conference, ensuring the voices of people living with WM

A simple winter flu checklist for people living with Waldenström’s macroglobulinaemia (WM) and LPL. Learn what symptoms to watch for,

WMUK’s Active Monitoring Checklist will appear alongside seven other innovations from partners within the Cancer52 alliance, all working to improve
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.

We’re delighted to introduce Rachel, our new WMUK Support Nurse. We caught up with her for a chat about her

WMUK fact-check some of the myths & misunderstandings around the rare blood cancer, Waldenstrom’s macroglobulinaemia.

Blood cancer may often be called a “hidden cancer,” but together we can make sure it’s anything but hidden this

From January 2026, patients diagnosed with long-term conditions will be automatically referred to trusted charities via the new government-backed Diagnosis

On the 3 July the government published its 10 Year Health Plan, after months of consultation with the public, NHS

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

As part of Volunteers Week, we spoke with Kevin, one of WMUK’s volunteer buddies. He shares his journey with Waldenstrom’s

Mental health, information and diagnosis were highlighted as areas of focus for the WM community. Last summer, over 500 patients,