The International Waldenstrom's Macroglobulinemia Foundation (IWMF) is a patient-funded and patient-driven nonprofit organization dedicated to supporting individuals affected by Waldenstrom's Macroglobulinemia, a rare disease. They provide comprehensive resources, answers to questions, and support for those newly diagnosed, as well as a community of individuals who understand the challenges of living with this condition.
The IWMF also offers educational forums, events, and support groups, allowing individuals to connect with others facing similar experiences. Through their research initiatives, they strive to advance understanding and treatment options for Waldenstrom's Macroglobulinemia. With the IWMF, individuals and their caregivers are never alone in their journey with this rare disease.
Generated from the website