I decided to publicize my experience as a person suffering from Waldenström’s macroglobulinemia (WM) because, regardless of the importance of sharing...
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 decided to publicize my experience as a person suffering from Waldenström’s macroglobulinemia (WM) because, regardless of the importance of sharing...
The Forum was sponsored by the IWMF and Hematon (the Dutch blood cancer organization) and followed the 9th International Workshop on WM (IWWM9). The attendees...
Thanks to researchers and to clinical trial participant patients around the world, and as a result of research funded by the IWMF and its International...