The UK charity for Waldenstrom’s macroglobulinaemia – a rare type of blood cancer
Support Line: 0300 373 8500

Meet Rachel: WMUK’s New Support Nurse

rachael harris meet the new support nurse

We’re delighted to introduce Rachel, our new WMUK Support Nurse. We caught up with her for a chat about her background, her career in haematology, and her life outside of work.

Busting Myths About WM

Busting Myths About WM

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

September is Blood Cancer Awareness Month

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

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?

What does the NHS 10 year plan mean for those with WM

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.

Jane Hockley, WM Buddy

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.

A New Chapter in WM Research

Rory Morrison WM Registry Closes

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

Buddy Q&A with Kevin

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.