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Research, treatment & care for patients with Waldenstrom's Macroglobulinemia.
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This is the official website for the International Workshops on WM. Starting with the First International Workshop for WM in Washington DC in Sept. 2000, workshops have been held bi-annually, the most recent in October of 2018 in New York City, USA. The next workshop is scheduled to be held in October of 2022 in Madrid, Spain. These workshops provide a venue for the WM scientific community to collaborate and share their latest research with the goal of advancing the knowledge of the genetic basis and pathogenesis of WM, and the development of theraputics for this malignancy.
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The IWMF provides a means for those with Waldenstrom’s Macroglobulinemia, doctors and others with an interest in the disease, to find mutual support and encouragement. The IWMF provides information and educational programs that address patients’ concerns, and promotes and supports research leading to a cure.
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This is the official website for the International Patient/Physician Summits on WM.
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The support group includes information resources from the medical community involved in the research and treatment of Amyloidosis.
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The definitive resource for information on blood cancers. Log on to find the latest news on disease characteristics, diagnosis and treatment, clinical trials, and breaking research findings.
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A support website by patients for patients with Cold Agglutinin Disease.
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This is a central point for information for UK members, newly diagnosed and other interested parties as well as UK doctors who we hope will eventually use this as a medium to inform WM suffers of ongoing research projects and clinical trails as well as any other information they wish publicized.
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Dr. Jorge J. Castillo is the Clinical Director of the Bing Center for Waldenstrom's Macroglobulinemia Clinic, located at the Dana-Farber Cancer Institute, Boston, MA. The Bing Center Clinic is dedicated to the treatment and care of patients with Waldenstrom's Macroglobulinemia and related IgM disorders.
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The EWMnetwork is intended to create an umbrella organisation for all European WM patient support groups or patient support organisations. The EWMnetwork was initiated by representatives of European patient organisations from Belgium, The Netherlands and UK in co-operation with the US based International Waldenstrom's Macroglobulinemia Foundation (IWMF). The EWMnetwork emphasizes exchange of information between WM patient support organisations and such questions as accessibility to treatment, medication, trials and stimulation of research on a European level.
