The IWMF’s new online community, IWMF Connect, enables participants to connect with each other via either email or an online discussion board format....
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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The IWMF’s new online community, IWMF Connect, enables participants to connect with each other via either email or an online discussion board format....
The walk will take place at the IWMF Patient Educational Forum in Phoenix, Arizona. This year, during the 1st Annual Walk for Waldenstrom’s, besides getting...
Eva Hoff Wanderaas, MD and PhD, a WM patient and member of the IWMF and WM-Scandinavia, decided that “she would try her hand” at translating a few of the...