In the past few years there has been an explosion of research and discoveries in immunologic and genetic aspects of WM. The IWMF is pleased to provide the...
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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In the past few years there has been an explosion of research and discoveries in immunologic and genetic aspects of WM. The IWMF is pleased to provide the...
The worldwide coronavirus outbreak, declared a pandemic by the World Health Organization (WHO) on Wednesday, March 11, continues to be of great concern to WM...
This new IWMF Affiliate will be based in Oporto and provide education and support to all WM patients and caregivers across Portugal. Leadership for APLL/WM...