This is a paid clinical trial advertisement.
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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.
July 9, 2021 – 1:30 PM EDT
May 4, 2021
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!
GET the latest news from the IWMF HERE:
https://conta.cc/3iFgewL OR on our website at: https://tinyl.io/4Uw5
#waldenstroms #wmiwmf
REGISTER NOW for Triage Cancer's 7/20 webinar! Learn how stress can impact the body. Get concrete tools for managing intrusive thoughts, and more.
RSVP for FREE: http://triagecancer.org/webinars
#BeyondDiagnosis #OncoAlert #hcsm #TriageTalks
$CLRB Lisa Wise has faced a battle with #Waldenstroms since 1990. When the #COVID19 pandemic hit, she, along with her husband, faced even more challenges. Read her Story of Hope from @WMIWMF & read the full story from @nytimes #WM #BloodCancer #RareDisease
Lisa J. Wise: "Love Letter to My Husband in Day 18 of Quarantine" - International Waldenstrom’s Macroglobulinemia Foundation
Diagnosed with WM in 1990, Lisa Wise has been mindfully practicing social distancing long before it was popular...
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