IWMF Virtual Ed Forum 2022 Starts In:
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The 2022 Educational Forum Primer Series
View rebroadcasts from the October 6th 2021 Ed Forum WM Basics Workshop and NEW Q&A with our presenters! Please note that you will need to register to view the live and on demand webcasts.

WM & Basic Terminology

Genomics/Science of WM

Understanding Your Blood and Bone Marrow Tests
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.

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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.
IWMF Calendar of Events
Triage Cancer – Unpacking Cancer from the Back Pack
Triage Cancer – Unpacking Cancer from the Back Pack
International Waldenstrom’s Macroglobulinemia Foundation News
IWMF Adds New Board of Trustees and Research Committee Members
Dr. Stephen Ansell, MD, PhD, has agreed to join the IWMF Board of Trustees. Most WMers will recognize Dr. Ansell from his frequent presentations at IWMF...
Video Interview: Ibrutinib Therapy in WM
n the video, Jennifer Brown, MD, PhD, of Dana-Farber Cancer Institute and Richard Furman, MD, noted WM researcher/clinician from Weill Cornell Medical...
U.S. NCCN Releases New Treatment Guidelines for WM
Each year, the US National Comprehensive Cancer Network (NCCN) publishes updated treatment guidelines for various forms of cancer, including Waldenstrom’s...
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.
ABBREVIATED COVID-19 Letter to Share with Hospitals for Emergency Medical Events

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