Here’s how we can help:
Find answers
Newly diagnosed or living with WM long-term? Find out more about WM.
Get support
Talk to others, share your experiences, and live well with WM. Get support.
Research
The Rory Morrison WMUK Registry informs research to increase our understanding of WM, support access to new treatments and ultimately find a cure. Find out about WM research.
Support our work
We are incredibly grateful to everyone who supports our work.
Everything we do is funded entirely by voluntary donations, helping us to provide vital support to the WM community, and to find a cure
for WM.
Latest news
Raise WM awareness on Rare Disease Day
Around 4,000 people are currently living with Waldenstrom's macroglobulinaemia. As a rare disease, it's vital we raise awareness so that these people get the care and treatment they need.