WaldosNZ is New Zealand's patient-led support and advocacy group for people affected by Waldenström Macroglobulinemia. The organisation is run by a dedicated volunteer committee comprising Dr Ruth Spearing and Dr Samar Issa (Medical Advisors), Mel Arnold (Group Lead), Lea Hullett, Rick Robinson, and Barney Stephenson.
WaldosNZ is a Global Partner / Affiliate of the International Waldenström Macroglobulinemia Foundation (IWMF).
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WhiMSICAL
Waldenström Macroglobulinemia Study, a world-first, ethically-approved, comprehensive global database of patient—derived data about your WM journey.
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ANNUAL IWMF EDUCATIONAL FORUMS
Learn about WM by watching presentations from the top international WM experts.
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Rare Disorders
"No country can claim to have achieved universal healthcare if it has not adequately and equitably met the needs of those with rare diseases."
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