Wherever you are on your Waldenstrom’s macroglobulinaemia journey, we are here to help you live well. Find out how to connect with our expert-led Support Line, local Support Groups, find a WMUK Buddy and access webinars, events and resources.
Chat with a WM expert through our free, confidential phone line.
The WMUK Support Line is a confidential phone service that provides nurse-led support for patients at any stage of their WM journey as well as friends and family who are supporting a loved one with the condition.
You may be newly diagnosed, have questions about symptoms or treatment, want to chat things through before a healthcare check-up or just feel like you need to speak to someone who understands what you’re going through. Our team can provide immediate support and direct you to other charities and organisations that may be able to help.
The support line is open Monday to Thursday 9am-5pm.
Call our support line
Speak to a WM expert about absolutely anything.
Meet other WM patients and families in your area or at a similar phase of life.
We have 11 regional support groups, and 4 support groups for those with specific WM experiences, such as mums, families and carers with WM. Groups meet online and in person to share stories, experience and encouragement.
Explore webinars, information guides and other resources on WM
Explore a host of information to help you understand what WM, diagnosis, treatment and how to live well with the condition. There’s also helpful signposts to other websites and organisations who offer specific support.
Join our Support Line Nurse, Beth for an informal online drop in session.
Every month, Beth runs an hour-long, drop-in session where patients share experiences and ask questions about anything WM related. There is no need to register, just visit our event page to find details of when the next session.
Explore online and in person events to support everyone impacted by WM.
See a full lists of the events we’ve got coming up. These include expert-led webinars, Coffee and Chat sessions and in person events, including our Patient Summits. The page is updated as we add events.
We match WM patients seeking one-to-one peer support with volunteer Buddies who are also living with WM. It’s a chance to speak to someone who understands what it’s like to live with a rare cancer.