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 International Waldenstrom’s Macroglobulinemia Foundation (IWMF) encourages you to register today for this free educational webinar with Dr. Edward...
After 8 years of leadership, Carl Harrington, Chair of the International Waldenstrom’s Macroglobulinemia Foundation (IWMF) Board of Trustees, will be...
The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is excited to announce the addition of two new members to the Board of...
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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