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

WMUK is a community of experts

Working hard to provide up to date information and personal support for people affected by Waldenstrom’s macroglobulinaemia (WM), a rare form of blood cancer.

We aim to improve understanding and access to treatment and care to ensure everyone with WM can live longer, better quality lives.

We do this through the dedication and support of donors and fundraisers, without whom the charity and its resources would not exist. Help us to continue helping the WM community here.

Where would you like to start?

WMUK understand the challenges and uncertainties that come with a Waldenstrom’s macroglobulinaemia blood cancer diagnosis. That’s why we offer a range of support services tailored to meet the diverse needs of patients and their families.

Information and ResourcesExplore a wealth of information and resources on Waldenstrom’s macroglobulinaemia, covering treatment options, specialist centres, and invaluable guidance for patients, caregivers, and those newly diagnosed.

Community and SupportJoin our nurturing community through our support groups and online Facebook groups. Reach out to our dedicated helpline team for personalised support and guidance.

Updates and EventsStay updated on our latest news, campaigns, and events, including regular online meet-ups, expert webinars, and the annual patient forum.

Your WM Journey

Find nearby support groups for Waldenstrom’s macroglobulinaemia, or contact our support line.

WM Support Line

WMUK telephone support line offers support, advice, and signposting, Monday to Thursday from 9 AM to 5 PM

WM Resources

A wealth of webinars, documents & links about Waldenstrom’s macroglobulinaemia

Finding Support

Find nearby support groups for Waldenstrom’s macroglobulinaemia, or contact our support line.

Treatment

Explore our comprehensive guide to receiving treatment for Waldenstrom’s macroglobulinaemia

Your starting to point to find out all about the rare blood cancer, Waldenstrom’s macroglobulinaemia (WM).

WM Events

Support groups, meetings, & more

January 2025

30
Thursday 30 January 2025
19:00
Webinar

Online webinar

We recognise the particular barriers to accessing mental health services for men. That’s why we’re delighted to be joined by Tough to Talk, a charity that focusses on raising awareness of men’s mental health.

Webinar
30
Thursday 30 January 2025
19:00 - 20:00

For people affected by WM, living in Scotland. This group meets on Zoom to chat, share experiences and exchange advice.

To join email us: support@wmuk.org.uk

February 2025

20
Thursday 20 February 2025
19:00 - 20:00
Register here

Professor Diana Greenfield, Consultant Nurse in Late Effects (of cancer treatment) at Sheffield Teaching Hospital, will be joined by a WMer with lived experience of the late effects of treatment. They’ll discuss what late effects are, and how self-empowerment can help to live well with WM. 

Register here
25
Tuesday 25 February 2025
19:00 - 20:00
Join Coffee and Chat

Join our Support Line Nurse, Beth, for an informal drop-in session. This is a chance to ask questions and listen to stories from others in the WM community. No need to register, just join anytime during the hour long session using the button below.

Join Coffee and Chat

March 2025

10
Monday 10 March 2025
19:00 - 20:00
Join here

Join our Support Line Nurse, Beth, for a special Coffee and Chat session focussed on peripheral neuropathy. This condition affects many people with WM, and the informal drop-in session will be a great way to ask any questions or get support from others in a similar situation.

Join here
26
Wednesday 26 March 2025
19:00 - 20:00
Join here

Join our Support Line Nurse, Beth, for an informal drop-in session. This is a chance to ask questions and listen to stories from others in the WM community. No need to register, just join anytime during the hour long session using the button below.

Join here

Give back to keep our services running

We can’t do what we do without your support. WMUK receives no government funding, and relies solely on voluntary donations and fundraising to keep its services open. Join the community and give back. Your support will make sure everyone can access the information and support they need, when they need it.