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) Board of Trustees has reviewed and approved funding an additional $500,000 to renew...
The IWMF is proud to announce the addition of five new physicians to our prestigious physicians directory. WM specialists from Argentina, Greece, Israel,...
The International Waldenstrom’s Macroglobulinemia Foundation invites you to join us for the third installment in our 2020 IWMF Global Educational...
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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