Many of you may already recognize Shirley, as she has served for several years as the support group leader in the Seattle, Washington area, and most recently...
International Waldenstrom’s Macroglobulinemia Foundation
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HOW CAN THE IWMF HELP?
Newly Diagnosed?
Getting a diagnosis of WM can feel overwhelming. You have questions, we have answers! Tap in to our comprehensive resources about this rare disease.
Get Support
We are here to support you throughout your journey living with Waldenstrom macroglobulinemia. Remember, with the IWMF, you are never alone.
Join Us
When you join the IWMF, you become a member of an international community of people affected by Waldenstrom macroglobulinemia.
ABBREVIATED COVID-19 Letter to Share with Hospitals for Emergency Medical Events
The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is offering its official statement for hospitals regarding prioritizing Waldenstrom’s macroglobulinemia patients when triaging care during the COVID-19 Pandemic. We recommend that all WM patients have this letter handy and available
when visiting an ER in the event that they may have COVID-19.
Stay Safe – Stay Healthy – Stay Waldenstrong!
IWMF Virtual Ed Forum 2022 Starts In:
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IWMF Calendar of Events
Eastern MA Support Group Meeting
Eastern MA Support Group Meeting
Date: May 22, 2022Time: @ 1:00 pm- @ 3:00 pm
E. PA & S. NJ (Philly) Support Group Meeting
E. PA & S. NJ (Philly) Support Group Meeting
Date: May 22, 2022Time: @ 2:00 pm- @ 4:00 pm
IWMF and CancerCare’s Waldenstrom’s Macroglobulinemia (WM): Treatment Progress Workshop
IWMF and CancerCare’s Waldenstrom’s Macroglobulinemia (WM): Treatment Progress Workshop
Date: May 25, 2022Time: @ 1:30 pm- @ 2:30 pm
International Waldenstrom’s Macroglobulinemia Foundation News
IWMF Adds New Members to Board of Trustees: Ganse and Branscome
read more
WhiMSICAL Study: More Responses Needed in Quality of Life Survey
Investigators aim to present important WM Quality of Life data at International Conference – YOUR HELP IS NEEDED! A huge congratulations and thank you to the...
Ryan Scofield’s Story: “We’re All in This Together”
Ryan’s story was first published in the in the IWMF Torch, January 2015, page 21. This is an update to that story. I was diagnosed with WM in 2010 when I was...
Stories of Hope
People with Waldenstrom macroglobulinemia and their caregivers share how they have coped living with this rare disease. Learn from these inspirational stories.
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The IWMF Twitter Feed
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We hope you enjoyed Wednesday's first in our WM Primer Series-WM and Basic Terminology. View the replay here: https://tinyurl.com/iwmfevents-2022-3
Register now for the second in our series, Genomics/Science of WM here: https://tinyurl.com/iwmfevents-2022-4
TOMORROW! REGISTER NOW for the first installment of the IWMF WM Primer Series: WM & Basic Terminology with Dr. Jeffery Matous, May 18th at 1:30PM EDT. Have your questions ready for the LIVE Q&A!
Register HERE: https://tinyurl.com/iwmfevents-2022-3
REGISTER NOW! WM & Basic Terminology with Dr. Jeffery Matous will be broadcast on May 18th at 1:30PM EDT. Join in the LIVE Q&A!
Register HERE: https://tinyurl.com/iwmfevents-2022-3
