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Stay up to date with the latest developments in myasthenia gravis research, advocacy, and community support. Explore news, events, and policy updates to stay informed and get involved.

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Keeping track of your life when managing Myasthenia
April 29, 2021

Association Management committee members regularly suggest that people keep a diary of their symptoms, medications, lifestyle impacts etc. in preparation for their visits to the Doctor.

Consumer Research Survey – IVIg
April 17, 2021

NPS MedicineWise is looking for people who have been prescribed immunoglobulins (antibodies) as part of their treatment to take part in a short survey online and/or an in-depth interview over the phone.

COVID-19 VACCINATION QUESTIONS?
January 9, 2021

The consensus of the Doctors is that ALL patients with Myasthenia should be vaccinated.

IMPORTANT MESSAGE FROM MAA MEDICAL ADVISORY BOARD
September 26, 2020

Anybody who has previously had or currently has a thymoma should take extra care protecting against exposure to COVID 19.

CURRENT RESEARCH TRENDS AND HOW WE CAN TAKE ADVANTAGE!
July 11, 2020

It is critical that we, as a community, embrace the on-line survey approach to learning more about MG.

RARE DISEASE DAY – 29 FEBRUARY, 2020
February 28, 2020

Susan White, MAA President, is delighted to be attending the Parliamentary Event to be held in Canberra, on Wednesday, February 26th in celebration of Rare Diseases Day.

National Strategic Action Plan for Rare Diseases
February 21, 2020

Susan White, MAA President, is delighted to be attending the Parliamentary Event to be held in Canberra, on Wednesday, February 26th in celebration of Rare Diseases Day.

Inform your Federal Member Please!
January 10, 2019

The letter requesting support in applying for Rituximab treatment in Myasthenia to be included on the PBS has gone to Minister Hunt.

MG Versus Mgen
January 5, 2019

An unfortunate media release occurred in July this year.