WMozzies is an Australian non-profit organisation supporting people affected by Waldenström’s macroglobulinemia (WM), their families and the wider WM community. Its work combines practical support and accessible information with advocacy for research and improved access to treatment. The organisation liaises with research bodies and government to promote the discovery and availability of new WM treatments.

WMozzies offers resources to help people understand the condition and navigate support options, including information brochures, booklets, fact sheets, educational presentations and videos, newsletters, and a library of publications. Its website also provides details about Australian WM clinical trials, management guidelines, research projects, and a directory of Australian doctors. Members and visitors can find support contacts and information about services provided by the Leukaemia Foundation and the International Waldenstrom’s Macroglobulinemia Foundation (IWMF).

The group shares news and event updates and highlights WhiMSICAL, an IWMF patient registry available through an app. Through these resources and community connections, WMozzies helps Australians affected by WM access information, support, and opportunities to contribute to research.