The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a non-profit support and information organization for individuals with Waldenstrom’s macroglobulinemia (WM.) IWMF publishes a quarterly magazine with information about symptoms and treatments, stories of interest, articles about living with the disease and patient education. Comprised of more than 10,000 members, the organization offers a telephone and email service, a network of support groups around the world, and an online discussion forum. IWMF holds an annual Educational Forum for patients and supports a robust research program to fund projects aimed to better understand the disease.
The next Educational Forum will be held in Seattle, WA from June 24 – 26, 2022.
For more information about IWMF, click here.