September is Blood Cancer Awareness Month

Blood cancer may often be called a “hidden cancer,” but together we can make sure it’s anything but hidden this September. By raising awareness, sharing knowledge, and supporting one another, we can bring hope, encouragement, and light to everyone affected.
Government Launches Diagnosis Connect

From January 2026, patients diagnosed with long-term conditions will be automatically referred to trusted charities via the new government-backed Diagnosis Connect service. While it will initially cover diabetes, mental health, and lung conditions, WMUK is advocating for rare cancer patients to be included and highlights the importance of accredited information.
The 10 Year HealthPlan – what does it mean for the WM community?

On the 3 July the government published its 10 Year Health Plan, after months of consultation with the public, NHS staff, organisations, industry and partners. The ambitious plan outlines the government’s vision for the NHS with both short- and long-term changes. In Autumn 2024, WMUK consulted with the WM community about the changes you wanted […]
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 Service, she’s helping others navigate the same journey—offering empathy, reassurance, and a reminder that life doesn’t end with a diagnosis.
Government Shares Update on 10-Year Health Plan

The UK government released new details outlining the next phase of its 10-Year Health Plan.
A New Chapter in WM Research

From 1st July 2025, the Rory Morrison Registry is closing. The next chapter puts ensures the WM community shapes the future of care, research, & support.
Q&A with Kevin: Why I Became a Buddy for WMUK

As part of Volunteers Week, we spoke with Kevin, one of WMUK’s volunteer buddies. He shares his journey with Waldenstrom’s macroglobulinemia (WM), his motivation for becoming a buddy, and why he believes this simple act of connection can make a profound difference.
The Big WM Survey – driving change for WM patients and families

Mental health, information and diagnosis were highlighted as areas of focus for the WM community. Last summer, over 500 patients, family members, friends and carers completed the Big WM Survey, run by WMUK. The results have shed light on key areas of support needed by people affected by Waldenstrom’s macroglobulinaemia (WM) to help them live […]
WMUK launches Winter Fuel Fund

If you’re struggling with heating bills this winter, WMUK is here to help with our Winter Fuel Fund
The festive calendar at WMUK

Everything you need to know about accessing our WM support and events over Christmas and into the New Year.