The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a patient-founded, patient-led, international non-profit that is dedicated to a simple but compelling vision: Support everyone affected by Waldenstrom’s macroglobulinemia (WM) while advancing the search for a cure. Since 1996, IWMF has funded over $10 million in WM research and provided an array of informative resources for patients, caregivers, and medical professionals. These resources include events, support groups, booklets, a quarterly newsletter, videos featuring top WM researchers, and more.
To learn more, we encourage you to visit http://www.iwmf.com/.
The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a patient-founded, patient-led, international non-profit that is dedicated to a simple but compelling vision: Support everyone affected by Waldenstrom’s macroglobulinemia (WM) while advancing the search for a cure. Since 1996, IWMF has funded over $10 million in WM research and provided an array of informative resources for patients, caregivers, and medical professionals. These resources include events, support groups, booklets, a quarterly newsletter, videos featuring top WM researchers, and more.
To learn more, we encourage you to visit http://www.iwmf.com/.