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.

On our YouTube channel, you can find a variety of videos from Waldenstrom's Macroglobulinemia experts, patients, and caregivers from events like our annual Educational Forum. To learn more about IWMF, we encourage you to visit http://www.iwmf.com and become a member for the latest in WM news, advocacy, events, and more.

Please click the link below to visit our YouTube channel: