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Supporting you to live well with WM

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.

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WMUK is a community of experts and fellow ‘WMers’, working tirelessly to offer advice, support and a friendly face you can rely on.

WMUK is the only charity in the UK dedicated to offering support, information and research for people living with Waldenstrom's macroglobulinaemia.

 

We offer support and information for people diagnosed with WM and their families, provide expert insight to healthcare professionals through our clinical networks and support research into treatments to improve the lives of people living with this rare blood cancer.

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What is
Waldenstrom's
macroglobulinaemia?

Your starting to point to find out all about the rare blood cancer,

Waldenstrom’s macroglobulinaemia (WM)

Upcoming Events

Want to know what’s on in the Waldenstrom's macroglobulinaemia world? From fantastic fundraising to our WM webinars, you can see at a glance what’s coming up.

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The UK charity for Waldenstrom's macroglobulinaemia

WMUK, Foden House, 47 London Road, Alderley Edge, Cheshire, SK9 7JT

© 2022 WMUK

General enquiries: 0300 303 5870

Registered as a charity in England and Wales (1187121).

Support Line: 0300 373 8500

A company limited by guarantee in England and Wales (12358324).

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WMUK is the only charity in the UK focused solely on Waldenstrom's macroglobulinaemia (WM), a rare type of blood cancer.

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