Rare Cancer Bills – what it means for the WM and LPL community
The Rare Cancers Act is an important moment for people diagnosed and living with rare cancers, including WM and LPL.
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News, updates, research & information about WMUK’s work around Waldenstrom’s Macroglobulinaemia.
The Rare Cancers Act is an important moment for people diagnosed and living with rare cancers, including WM and LPL.
The National Cancer Plan for England promises to spotlight rare cancers like WM and LPL, targeting earlier diagnosis, fairer access
A guide to understanding your immune system with WM or LPL, including vaccinations, infection advice and simple ways to stay
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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,
If you’re struggling with heating bills this winter, WMUK is here to help with our Winter Fuel Fund
Everything you need to know about accessing our WM support and events over Christmas and into the New Year.
WMUK is registered with online giving platforms that donate to WMUK when you shop with certain retailers online.
The WM-VOICE study is looking for UK patients to share their views anonymously as a part of first-of-its-kind study, looking