The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a trusted organization dedicated to providing support, education, and resources for individuals affected by Waldenstrom's macroglobulinemia (WM). WM is a rare type of non-Hodgkin lymphoma. With a comprehensive range of services, the IWMF aims to help patients and caregivers navigate their WM journey.

Through their website, the IWMF offers information on the causes, symptoms, and diagnosis of WM, helping newly diagnosed individuals understand their condition. They also provide resources for organizing medical records and getting a second opinion. The IWMF offers support through a directory of WM physicians, US and international support groups, and real-life stories of hope.

They also connect patients and caregivers through online discussion forums and provide financial assistance options. Furthermore, the IWMF is committed to the research and healthcare community. They offer educational resources, research grants, and medical practice guidelines.

The IWMF welcomes donations, encourages fundraising activities, and advocates for awareness and progress in WM research. Join the IWMF and become part of a supportive, international community dedicated to improving the lives of those affected by WM