Support Line: 0300 373 8500
Join us this September as we raise the profile of blood cancer, bust cancer myths, share accurate information, and support each other.
This year WMUK is bringing personalised patient support and expert information to your region.
Learn about clinical trials for Waldenstrom’s macroglobulinaemia, find out how to take part, & discover trials that are currently running in the UK
Waldenstrom’s macroglobulinaemia (WM) is a rare type of blood cancer. It has its own distinct characteristics that require specialised treatment and care. Our vision is that people affected by WM live longer, good quality lives supported every step of the way by WMUK.
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.
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 Resources: Explore 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 Support: Join 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 Events: Stay updated on our latest news, campaigns, and events, including regular online meet-ups, expert webinars, and the annual patient forum.
Find nearby support groups for Waldenstrom’s macroglobulinaemia, or contact our support line.
WMUK telephone support line offers support, advice, and signposting, Monday to Thursday from 9 AM to 5 PM
Find nearby support groups for Waldenstrom’s macroglobulinaemia, or contact our support line.
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).
Starting this September, our CEO Jane Nicholson and our Acting Chair of Trustees, Dr Harriet Scorer, will be hosting an informal online session.
They’ll be sharing what’s happening behind the scenes, the plans we’re shaping, and ideas currently in development.
Most importantly, this is your chance to ask us about anything—from funding and partnerships to the support you’d like to see us develop.
As a small community, these catch-ups are a space for honest conversation, where together we can focus on the things that matter most.
Register to join us:
Register Now
This will be our second time running this course with very positive feedback from the first. This will be a 4 week course 1 hour a week to be run by Henrietta Gyori from the charity. We ask that you have a straw, a 1/3 full glass of water and a cotton ball. More information can be found on the following links
Website: https://www.voh.org.uk/
The third part of WMUK’s regional patient summits for 2025 will take place in Belfast, Northern Ireland.
Full details of Northern Ireland WM Patient Summit are yet to be announced but you can register your interest on the link below.
More Info Join us at our chair yoga and relaxation session. This will be a 45 minutes session taken by Sue, please have water and a blanket to hand you may require blanket for the relaxation as your body temperature can drop.
Register
Join to chat with other WMers about your experiences of living alone. It’s a drop in event, so you’re welcome to come for the whole hour or just pop in for 5 minutes.
Join on Zoom
Chat with Anna at Menopause and Cancer, how they can support you.
WMUK round-off 2025’s regional summits, with this event in Birmingham, England
Full details are yet to be announced but you can register your interest on the link below, or attend one of our other regional events in Scotland, Wales & Northern Ireland.
More InfoPhone support, regional groups, & online forums supporting people affected by WM
Answers to some of the most common questions for those newly diagnosed with WM
Symptoms vary from person to person. Here we describe some of the most common symptoms.
Everything you need to know about the different treatments available for WM
An introduction to diet, exercise, symptom management, mental health support, and work-life balance.
A easy to understand explanation of Waldenstrom’s macroglobulinaemia
Explore & download our guides, watch webinars, find factsheets and more in our library
Find out what happens if you’ve been in remission, and have a relapse.
The Registry collates information for medical professionals about this rare cancer
