- Waldenstrom’s Weekly – April 12, 2024
- THANK YOU! Giving Challenge – 2024
- Lisa Wise Featured in LLS Video
- IWMF Torch – April 2024
- First-Ever WM World Awareness Day
- European WM Patient Forum – New Post-Meeting Q&A Video Available!
- The Global Patient Survey on Lymphomas & CLL
- Expansion of IMBRUVICA® (ibrutinib) Label in the U.S.
- 2024 IWMF Educational Forum
- Facebook Fundraising Guide Available!
- Recording Available! Nutrition: Fuel for Your Body
- IWMF Mourns Death of Board Member, Glenn Cantor
- IWMF Launches Accelerate the Cure Campaign on Rare Disease Day
- Research Study Outcomes for Caregivers
With the IWMF You Are Never Alone
The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a patient-funded and patient-driven, nonprofit organization that is dedicated to a simple but compelling vision.
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.
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Stories of Hope
People with Waldenstrom’s macroglobulinemia and their caregivers share how they have coped living with this rare disease. Learn from these inspirational stories.
Julie Davidson: My Journey With WM and Bing-Neel Syndrome
Julie Davidson: My Journey With WM and Bing-Neel Syndrome Published in the Torch 23.2 (April...
CALENDAR OF EVENTS
BMT InfoNet Survivorship Symposium – VIRTUAL
BMT InfoNet Survivorship Symposium - VIRTUAL
IWMF Educational Forum
IWMF Educational Forum
Triage Cancer Webinar: Caregiving
Triage Cancer Webinar: Caregiving
How Can We Help You?
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