Here for everyone impacted by WM
WMUK is the only charity in the UK focused on supporting people affected by Waldenstrom’s macroglobulinaemia (WM)
We help people with Waldenstrom’s macroglobulinaemia (WM), a rare form of blood cancer, live longer, better-quality lives. We do this by providing essential resources, information and support for patients, families, and healthcare professionals.
Everything we do is led by the needs of WM patients and their families. Following extensive consultation with our community, we developed a five-year strategy based around four core pillars. As an organisation, we aim to:
Be the expert voice of WM – the most credible leading-edge source.
Empower patients to live well with WM and support them throughout their WM experience.
Be financially viable organisation with a strong foundation for achieving our goal.
Our latest Impact Report highlights all that we’ve achieved in the past year to help shape better care and stronger support for everyone affected by WM. From expanding our nurse-led support line and organising webinars, to producing more resources than ever and advocating on behalf of WM patients.
Our Board of Trustees, WMUK Team, and Patient Advisory Group work closely together to deliver support and resources for our WM community.
WMUK’s core team manages the day-to-day running of the charity and its activities. The team develops resources, connects with healthcare professionals, produces information, and provides direct support to WM patients and their families.
We are looking for new trustees with legal, governance, finance, HR, and fundraising expertise to help strengthen our current board. If you would like to find out more about the role, please email info@wmuk.org.uk.