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The Australian patient support group for Waldenström’s macroglobulinemia
WMozzies provides information and support to the Australian Waldestrom’s macroglobulinemia (WM) community. WMozzies works closely with research organisations and government to actively promote the discovery and availability of exciting new WM treatments.
The group is an affiliate member of the IWMF who provides the following services for WMozzies members around Australia:
- To meet the needs of patients, caregivers, and families touched by WM.
- To be the place where people can learn from others affected by the disease, gain important knowledge about resources for help, and learn about advances in medicine and treatments.
- To help you understand and cope with the illness so that you know that you are not alone.
- To connect you to IWMF members around the world who understand and share experiences.
- To connect on a one-on-one basis with someone who understands and is living with WM.
- To assist If you should need a second medical opinion for your illness.
- To share WM patient stories.
WMozzies is also closely affiliated with the Leukaemia Foundation who provide Aussie WM patients and their families with a range of practical and emotional support. Find out more at leukaemia.org.au/our-services.
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Contact WMozzies leader, Andrew Warden, by phone 0408 303 718 or by email andrew.warden@bigpond.com
