Contact

  • 6144 Clark Center Ave.Sarasota, FL 34238
  • Phone: 941-927-4963
  • Fax: 941-927-4467
  • [email protected]

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.

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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.

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CALENDAR OF EVENTS

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