I’ve come to learn that none of us with WM has a “typical” journey. This very rare blood cancer affects us all so differently, not just with symptoms,...
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.
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.
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I’ve come to learn that none of us with WM has a “typical” journey. This very rare blood cancer affects us all so differently, not just with symptoms,...
On Tuesday, April 2, 2019, the Patient Access Network (PAN) Foundation announced a new patient assistance program for people living with WM. Qualifying...
On Wednesday, April 10, from 12:30PM to 1:30PM US Eastern Time, CancerCare, in collaboration with the IWMF, will be hosting an online/phone workshop on the...