This is a paid clinical trial advertisement.
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 very own Vice-Chair of Information & Support, Lisa Wise, was published in The Boston Globe with a moving story about her brother, a front-line...
IWMF COVID-19 News Brief – January 2021 While the coronavirus (COVID-19) pandemic continues to affect the global community, several vaccines have either been...
2021 IWMF GLOBAL EDUCATIONAL WEBINAR February 9, 2021 at 1:30PM U.S. ESTWhy Clinical Trials Matter and How to Find the Right One for You With Neena Kennedy,...
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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