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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REGISTRATION OPEN AT OUR NEW EVENTS SITE! IWMF Global Educational Webinar July 9, 2021 at 1:30PM U.S. ET The IWMF is excited to share that we have a new...
As many of you in the US are now aware, the CDC issued new recommendations for fully vaccinated people in non-healthcare settings...
To the IWMF Community, We want to let you know that after very careful consideration and with input from our WM medical experts, we have made the decision...
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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