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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“In the light of the COVID-19 pandemic, the International Workshop on Waldenström Macroglobulinemia (IWWM) Treatment Recommendations Panel felt the need...
This is the second in a series of three videos recently produced for the IWMF. In this video, Bob Rupert, a WM patient, discusses how WM has affected his life...
Edward Kemp: Ed’s Second Act [This is an update on Ed Kemp, a member of the IWMF community, whose original Story of Hope was published in 2015] Since 2015, my...
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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