The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a patient-founded and volunteer-led nonprofit organization dedicated to a simple but compelling vision: Support and educate everyone affected by Waldenstrom's macroglobulinemia (WM) to improve patient outcomes while advancing the search for a cure.
To accomplish this vision, the IWMF offers several invaluable benefits:
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Information for patients and caregivers written in easy-to-understand language.
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Education to help patients and caregivers learn about WM. Publications are available in multiple languages and our website reaches global patients in over 100 languages.
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On-going updates about the IWMF community at www.iwmf.com and through the quarterly IWMF Torch magazine and NEWS releases.
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Peer support from a worldwide network of patient groups, wellness program, social media, and online discussion forums.
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Research funding for better treatments and the search for a cure. Since 1999, the IWMF has funded over $30 million in global WM research
Website: www.iwmf.com
Phone: 202-496-1992
Email: info@iwmf.com