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MyClad Study clinical trial banner inviting Australians with myasthenia gravis to participate in MG research
Clinical Trial available in Australia!

The MAA is pleased to share with you that a clinical trial is now open for Australian participation. It will potentially offer an additional treatment pathway for myasthenia gravis patients. Please explore more details via the link provided. If you may be willing to participate, speak to your treating neurologist about progressing to the next…

Promotional image inviting people with myasthenia gravis to participate in MGAQ and QUT research exploring heat sensitivity, featuring a thermometer and heat-themed background.
Reminder: Have You Shared Your Experience of Heat and MG Yet?

Recently we announced an important research collaboration between the Myasthenia Gravis Association of Queensland and Queensland University of Technology. This is a gentle reminder that the survey is still open – and we would love to hear from you. Many people living with myasthenia gravis report that heat and hot weather can significantly worsen symptoms…

Myasthenia Alliance Australia Canberra event for Rare Diseases Day 2026
The MAA team are headed to Canberra!

Once again, it is time to celebrate with Rare Voices Australia (RVA) as they host a parliamentary event in honour of rare diseases day 2026. It is a privilege to have myasthenia gravis represented at this significant event and we express sincere appreciation to RVA for our inclusion. This meeting allows the MAA to speak…

VALUE-MG study update showing 216 people with myasthenia gravis recruited by Monash University research teams
VALUE-MG Study Update

Thank You to the Myasthenia Gravis Community The VALUE-MG study has officially reached its recruitment target, with 216 people living with myasthenia gravis participating across five hospital sites in Australia. This important research is helping build a clearer picture of how myasthenia gravis affects people’s health, daily activities and work over time, and how these…

Art with Heart 2026 campaign supporting Myasthenia Gravis awareness during International MG Awareness Month
Supporting MG Awareness with “Art with Heart” 2026!

The Myasthenia Alliance Australia (MAA) is proud to continue its important work during International June MG Awareness Month 2026. We need your help now to find items for our Art with Heart Auction to raise awareness of MG and build resources to support the important work of the MAA.  Get Involved and Make an Impact The first step…

Promotional image inviting people with myasthenia gravis to participate in MGAQ and QUT research exploring heat sensitivity, featuring a thermometer and heat-themed background.
Participate in a unique MGAQ research project: Share your experience about how heat affects you

Many people with myasthenia gravis report that heat and hot weather exacerbate their symptoms and impact their daily lives. However, little research has been performed to understand the exposures that trigger worsening symptoms or the broader impacts on daily life for individuals with myasthenia gravis. The Myasthenia Gravis Association of Queensland (MGAQ) is collaborating with…

Save the date graphic announcing upcoming MGAQ and QUT research project on heat and myasthenia gravis, featuring a bright heat-themed background and a thermometer image
Something big is coming for our MG community.

Look out for our new research project launching in the new year! The Myasthenia Gravis Association of Queensland is proud to share that we are working with Queensland University of Technology to explore Heat Sensitivity in People with Myasthenia Gravis. With input from leading specialists, including Dr Stefan Blum, we are developing a survey to gather…

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Nursing Excellence: The Vital Role of nurses in MG care

Nurses play a central role in supporting people living with myasthenia gravis, providing not only clinical care but also guidance, advocacy, and reassurance at every stage of the journey. In this recent Nursing Excellence webinar, Nurse Practitioner Jenny Stofmeel shared valuable insights into how nurses can support individuals with MG through personalised care, ongoing monitoring,…

Group photo from the Rare Disease Connect in Neurology meeting in Barcelona with patient organisation representatives, including the Myasthenia Alliance Australia
Rare Disease Connect in Neurology

Rare Disease Connect in Neurology – connecting with fellow patient organisations in Barcelona Rare Disease Connect in Neurology (RDCN) is an annual meeting that includes both healthcare professionals and patients. I was very honoured to be invited and sponsored by UCB to attend the 5th RDCN in Barcelona on behalf of the MAA and the…

Blue graphic with large word "you" and text saying you are the key to our success, promoting MG Vic Management Committee volunteer opportunities
MG Vic Management Committee.

MG Vic Management Committee. Passionate people like you could be the difference between achieving something good or something great for the Victorian MG community. MG Vic will not happen or thrive without Victorians making it happen – Your community is calling you. That’s why we’d love you to consider joining the MG Vic Management Committee…