The UK charity for Waldenstrom's macroglobulinaemia - a rare type of blood cancer
We know you want quick, easy to access information on WM for both you and your patients. You can find everything you need to understand more about WM, access educational information and better support your WM patients right here.
Documents, reports and factsheets
How the charity aims to grow support, information and access to treatment in the next five years.
A special issue of “memo inOncology”.
Commentary on: Uppal E. et al. The WMUK Rory Morrison Registry...
The 2nd report from the Rory Morrison WMUK Registry.
The authors distill current knowledge on the pathophysiology, epidemiology...
New (Dec 2021) guidelines produced by the British Society for Haematology...
13 September 2023
Dr Jin Lindsay covers all the basics for WM - great for people who are newly diagnosed or want to refresh their knowledge
7 June 2023
Learn what the charity is doing for WM patients and their ambitious plans for the future.
We're joined by Anthony Nolan, the charity that connects patients with stem cell donors, to talk about stem cell transplants in people with WM
Information on working rights and any benefits you may be entitled to.
A charity more focused to family members/carers on how to cope with caring for some one with a long-term condition.
Advice on working rights, rules and best practice.
A charity which focuses mainly on ‘Living Well with Cancer’ and has lots of resources around this.
Information about working and cancer.
A brilliant charity who focus on the non-clinical aspects of cancer including, finances, practical support, psychological support as well as support for carers.