Associated New Zealand ME Society: Difference between revisions

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ANZMES has been serving New Zealanders since 1980.
ANZMES has been serving New Zealanders since 1980.


==Online Presence==
==Online presence==
*[http://anzmes.org.nz/ ANZMES Website]
*[http://anzmes.org.nz/ ANZMES Website]
*[https://twitter.com/anzmes?lang=en ANZMES Twitter]
*[https://twitter.com/anzmes?lang=en ANZMES Twitter]

Revision as of 20:20, October 15, 2019

ANZMES logo.png

The Associated New Zealand ME Society (ANZMES) is a New Zealand group for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) patients and their caregivers.

Aims[edit | edit source]

  • Supporting ME patients and their carers in New Zealand.
  • Producing the quarterly magazine ‘Meeting Place’, informing members of the latest news, events and research pertaining to CFS/ME.
  • Procuring political support for the ME cause with the aim of bettering conditions for ME patients.
  • Facilitating communication between sufferers of the condition.
  • Acting as a respected national and international ‘voice’ on ME matters.
  • Encouraging research and education about ME.
  • Updating healthcare providers on the latest advances regarding this condition.
  • Co-ordinating and fostering the growth of local support groups throughout the country.
  • Providing information and resources to individuals and groups as required.

Funding[edit | edit source]

Notable people[edit | edit source]

Notable Studies[edit | edit source]

History[edit | edit source]

ANZMES has been serving New Zealanders since 1980.

Online presence[edit | edit source]

See Also[edit | edit source]

References[edit | edit source]