The IWMF’s new online community, IWMF Connect, enables participants to connect with each other via either email or an online discussion board format....
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.
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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
New IWMF Online and Email Community – Join Us!
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Reminder: First Annual Walk for Waldenstrom’s – May 21, 2017
The walk will take place at the IWMF Patient Educational Forum in Phoenix, Arizona. This year, during the 1st Annual Walk for Waldenstrom’s, besides getting...
IWMF Fact Sheets Are Now Available in Norwegian
Eva Hoff Wanderaas, MD and PhD, a WM patient and member of the IWMF and WM-Scandinavia, decided that “she would try her hand” at translating a few of the...
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
