Support Line: 0300 373 8500
Waldenstrom’s macroglobulinaemia (WM) and other types of lymphoplasmacytic lymphomas (LPL) are rare types of blood cancer. We’re here to give everyone affected by WM and LPL the knowledge and support they need to live longer, better quality lives.
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).
Join Sue on this gentle chair Yoga and Relaxation session. The relaxation session will be recorded for future reference.
Please have to hand some water and a blanket. Use the following link to register.
Register Now
Join Elaine for an in-person Scotland Support Group Meeting to be held at
the Cranachan Cafe
48 Buchanan St
Glasgow
G1 3JN
All are welcome to join, whether you are part of the support group or not. If you live over the border and can get to Glasgow you are more than welcome to come and see us also.
This will be a relaxed, informal catch up for those with WM, their carers, friends and family. All are welcome to share their journey, listen to others or just sit and enjoy the company.
If you would like any further information please contact carley.gray@wmuk.org.uk
Drop in for 5 minutes or stay for the hour we are here to chat, ask questions or just listen. You will find support from people who understand.
Join here Winwick Church Hall, Warrington, WA2 8TA
Please turn left into Church Walk and continue to Church Carpark.
This in person event will be hosted by Jane Rhodes fellow North West Support Group Member. On the day donations would be appreciated towards the costs of room hire and refreshments. If you would like to attend or have any questions, please email Carley, Community Support Navigator on carley.gray@wmuk.org.uk.
Drop in for 5 minutes or stay for the hour we are here to chat, ask questions or just listen. You will find support from people who understand.
Join Here Winwick Church Hall, Warrington, WA2 8TA
Please turn left into Church Walk and continue to Church Carpark.
This in person event will be hosted by Jane Rhodes fellow North West Support Group Member. On the day donations would be appreciated towards the costs of room hire and refreshments. If you would like to attend or have any questions, please email Carley, Community Support Navigator on carley.gray@wmuk.org.uk.
Phone 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