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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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It is with great pleasure that we announce Sue Herms as the 2020 recipient of the Judith May Volunteer Award. Under normal circumstances, Sue would have...
2020 IWMF Virtual Educational Forum August 27-28, 2020 This virtual experience will be available entirely online The 2020 IWMF Virtual Educational Forum is a...
[*The author, Kathy Horton, was featured in a recent article in Cure Today (Read Story HERE(link is external)), focused on how WM and other cancer survivors...
The Waldenstrom's Weekly is out! Read all about what's happening at the IWMF HERE: https://iwmf.com/the-waldenstroms-weekly-38/
#waldenstrom #bloodcancerawareness #iwmfshop
IWMF offers its official statement for hospitals regarding prioritizing WM patients when triaging care during the COVID-19 Pandemic. Have this letter handy & available when visiting an ER if they may have COVID-19.
DOWNLOAD NOW: https://tinyurl.com/IWMF-Letter
There is still time to support the IWMF - make your year end gift today!
DONATE: https://tinyurl.com/donateIWMF
#waldenstrom #newyear #donate
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