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.


IWMF Ed forum banner

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.