IWMF Virtual Ed Forum 2022 Starts In:
The 2022 Educational Forum Primer Series
View rebroadcasts from the October 6th 2021 Ed Forum WM Basics Workshop and NEW Q&A with our presenters! Please note that you will need to register to view the live and on demand webcasts.
WM & Basic Terminology
Genomics/Science of WM
Understanding Your Blood and Bone Marrow Tests
HOW CAN THE IWMF HELP?
Getting a diagnosis of WM can feel overwhelming. You have questions, we have answers! Tap in to our comprehensive resources about this rare disease.
We are here to support you throughout your journey living with Waldenstrom macroglobulinemia. Remember, with the IWMF, you are never alone.
When you join the IWMF, you become a member of an international community of people affected by Waldenstrom macroglobulinemia.
IWMF Calendar of Events
International Waldenstrom’s Macroglobulinemia Foundation News
IWMF President and WM patient Carl Harrington has written an article entitled “What To Do When Diagnosed With a Rare Cancer," published on the Cure magazine...
The IWMF’s newest International Affiliate, Macroglobulinemia De Waldenstrom Argentina, is based in Buenos Aires, Argentina, under the leadership of Graciela...
To provide the latest news on advances in WM research and treatments, and up-to-the minute information on our services to members, the IWMF will use both...