Alison Hunter Memorial Foundation
The Alison Hunter Memorial Foundation (AHMF) works independently, in a spirit of support and cooperation, with all researchers, institutions and ME/CFS societies to advance scientific knowledge and medical care.
The Foundation is an enduring memorial to Alison Hunter and all those whose lives have been devastated by ME/CFS.
Alison died in 1996, aged 19, from complications arising from ME/CFS which included seizures, paralysis, gastrointestinal paresis and overwhelming infection resembling Behcets Disease. Such complications are rare and only present in a severe subgroup. Alison courageously fought ME/CFS for ten years and was an unstinting advocate for young people.
Alison was the founding president of ME Young Adults (MEYA), established in 1992 at Royal North Shore Hospital, Sydney.
The AHMF was established in 1998 through the initiative of the Public Interest Advocacy Centre and The Public Interest Law Clearing House as a project of the law firm Minter Ellison.
The Alison Hunter Memorial Foundation is a non-profit institution.
Donations are gratefully received. For more information go to www.ahmf.org
Alison Hunter Memorial Foundation
PO Box 6132
NORTH SYDNEY NSW 2059
Australia
Phone/Fax:(02) 9958 6285
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Did you know?
As many as 180,000 Australians are directly affected by ME/CFS
Research
Research into ME/CFS is occuring across the globe. Follow the links below for research resources.
Alison Hunter Memorial Foundation
Australian Research Institutions
International Research Institutions
Support Organisations by State
ME/CFS Australia directs enquiries from members of the community about frontline support for people with ME/CFS to independently run state organisations.
Resources
Nutrition and ME/CFS: Download a PDF, available in the following languages:
Chinese(717 kb)Croatian(880 kb)Dutch(680 kb)French(740 kb)German(865 kb)Greek(821 kb)Italian(735 kb)Spanish(679 kb)Vietnamese(741 kb)
