For physicians interested in learning more about multiple myeloma, please visit MyelomaRevealed.com. →
To hear powerful stories from patients, physicians and others, visit Blood Counts, a national effort in collaboration with StoryCorps. →
Research and advocacy organizations play a significant role in the multiple myeloma community. They provide patient support, raise funds for research and drive disease awareness, among other roles. Visit the patient research and advocacy organizations below and find important information and a support group near you.
With more than 525,000 members in 140 countries worldwide, the IMF is dedicated to improving the quality of life of myeloma patients while conducting leading research aimed at prevention and a cure.
The mission of the Multiple Myeloma Research Foundation is to accelerate next generation multiple myeloma treatments to extend patients’ lives in pursuit of a cure.
The Myeloma Crowd provides patients with simplified myeloma education, funding for key myeloma research and data solutions to solve patient and research problems.
The Leukemia & Lymphoma Society's (LLS) mission is to cure leukemia, lymphoma, Hodgkin's disease and myeloma, and improve the quality of life of patients and their families.
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