To better support WM patients worldwide, IWMF Info Paks for Patients are now available in Chinese (Simplified & Traditional), French, Italian and Spanish....
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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To better support WM patients worldwide, IWMF Info Paks for Patients are now available in Chinese (Simplified & Traditional), French, Italian and Spanish....
This week is National Volunteer Week in the US. We should all take a moment to thank the volunteers who make the IWMF work for all of us. The IWMF is...
The IWMF and the WM Foundation of Canada have confirmed that, as of March 31, 2016, Health Canada has updated their “Notice of Compliance with Conditions...