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.
We help people with Waldenstrom’s macroglobulinaemia (WM), a rare form of blood cancer, longer, better-quality lives.
We do this by providing essential resources for patients, families, and healthcare professionals. Whether you need to speak to a WM expert, want to learn about the condition or are a healthcare professional who wants to support a patient more effectively, we can help.
As the go-to source for WM clinicians, we work closely with the NHS and are leading the way in gathering data about the condition to improve understanding and treatment.
We’re here to help people with WM live longer, better lives — with WMUK supporting them every step of the way.
Want to understand more about WM and what to expect at each stage of your journey? With the help of WM experts, we’ve created a range of resources to guide you along the way.
We’re ready to help you live well with WM – whether you’re looking to join a Support Group, learn how to manage your symptoms, or get one-to-one advice through our Support Line.
Take a look around and explore all the extra information and support we offer. From details on the latest clinical trial to guidance for friends and family, you’ll find what you need right here.
Be the first to know about new resources, events and other WM by signing up to receive our communications.
The WMUK Board is responsible for the direction and governance of the organisation. Board members include experienced leaders and specialists who bring diverse expertise to steer WMUK towards achieving its mission.
The Patient Advisory Group (PAG) comprises 20 volunteers with direct experience of WM. Members review patient information, give feedback on new resources, and contribute to new programmes and long-term strategies.
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.
The National Cancer Plan for England promises to spotlight rare cancers like WM and LPL, targeting earlier diagnosis, fairer access
A guide to understanding your immune system with WM or LPL, including vaccinations, infection advice and simple ways to stay
Advice and simple steps to help manage low mood and loneliness during the winter months, with support for people affected
This is an informal meeting – please use the link below to join. Feel free to take part in the conversation or simply listen in; there is no pressure to speak at all. In the interim, the session will be hosted by Carley, our Community Support Navigator.
If you have any questions, you’re more than welcome to email her at carley.gray@wmuk.org.uk
For anyone affected by WM in the East or West Midlands. Come together, share experiences and ask questions from others in a similar situation.
Join This is an informal meeting – please use the link below to join. Feel free to take part in the conversation or simply listen in; there is no pressure to speak at all. In the interim, the session will be hosted by Carley, our Community Support Navigator.
If you have any questions, you’re more than welcome to email her at carley.gray@wmuk.org.uk
Join This is an informal meeting – please use the link below to join. Feel free to take part in the conversation or simply listen in; there is no pressure to speak at all. In the interim, the session will be hosted by Carley, our Community Support Navigator.
If you have any questions, you’re more than welcome to email her at carley.gray@wmuk.org.uk
Join
Join Carley for this coffee and chat to support the carers and loved ones of WM patients. 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.
Use the link below to join.
Join