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Waldenström's Macroglobulinemia Support Group

WMozzies Aust. History of Waldos Contact
Waldenström's Macroglobulinemia New Zealand (known as Waldos) is an Affiliate of the
(IWMF) International Waldenström Macroglobulinemia Federation. We are an non-profit organisation.

Also known as a Lymphoplasmacytic Lymphoma (LPL), this very rare indolent Non-Hodgen's Lymphoma
has a world wide incidence of about five in a million people.
We aim to help you, live with, rather than worry about dying, of Waldenströms. Thanks to ongoing research and treatment options many WMers live much longer and with a better quality of life today.

Zoom meeting 12 May 2022

Screenshot from our May Zoom meeting.
Next Zoom meeting to be announced.

If you have WM or are a carer it's free to join us:
+ Meet and interact with others within NZ both in person and via Zoom meetings
Licence provided by the IWMF to enjoy virtual get-togethers.
+ Watch Webinars presented by top WM specialists throughout the world.
+ Be informed about all aspects of WM, current and new treatments.
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JOIN US FOR 27TH ANNUAL VIRTUAL EDUCATIONAL FORUM

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Ed Forum planning for 2022 is in the works! Our 27th annual Ed Forum will be entirely virtual this year. Experience expert-led programming for the Waldenstrom macroglobulinemia community from newly diagnosed patients, to 25+ year WM veterans, and everyone in-between. Check back here for the agenda and announcements.