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Support everyone affected by Waldenstrom's macroglobulinemia while advancing the search for a cure.
International Waldenstrom's Macroglobulinemia Foundation is a registered 501 (c)(3) organization dedicated to supporting everyone affected by Waldenstrom's macroglobulinemia through research, support, education, and advocacy. Waldenstrom's macroglobulinemia, also known as lymphoplasmacytic lymphoma (or LPL), is a rare form of non-Hodgkin's lymphoma with no known cure. Because less than 1,500 cases are diagnosed annually, Waldenstrom's is considered an orphan disease, making it difficult for researchers to secure funding and for patients to connect with one another. That's where IWMF comes in.
Led by an all volunteer board with a four person administrative staff headquartered in Florida, the IWMF is lean but powerful organization, and a force behind changes that have made an enormous impact on the understanding of WM and the prognosis for patients. Since 1994, IWMF has been a global force in helping promote research, spread awareness, and empower patients and caregivers. IWMF funded research contributed to the discovery of the first treatment approved specifically to treat WM. As the organization continues to fund and encourage research towards a cure, IWMF member services help patients, caregivers, and medical professionals around the globe make more informed healthcare decisions and connect the WM community locally and internationally.
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