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

The MAA Board urges people to complete a very short survey. It will help ensure more equitable access to treatments. Thank you in anticipation.

As people with a chronic illness, particularly inclusive of those who are immune suppressed, the Myasthenia Gravis community should be very familiar with the precautions needed ...

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.

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.

New information about medications that can worsen symptoms in patients suffering from myasthenia gravis (MG) has been published on the MAA website. This list is designed as an a...

New information about medications that can worsen symptoms in patients suffering from myasthenia gravis (MG) has been published on the MAA website. This list is designed as an a...

New information about medications that can worsen symptoms in patients suffering from myasthenia gravis (MG) has been published on the MAA website. This list is designed as an a...

New information about medications that can worsen symptoms in patients suffering from myasthenia gravis (MG) has been published on the MAA website. This list is designed as an a...

After months of planning the 2019 MAA Myasthenia Gravis Conference was huge success!