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Beyond the Symptoms: Supporting Psychological Wellbeing in MG
Living with myasthenia gravis (MG) can affect far more than physical health. The emotional and psychological impact of living with a chronic, fluctuating condition is an important part of the MG journey, and one that deserves greater conversation.
Join Myasthenia Alliance Australia (MAA) for the fourth webinar in our ‘Your MG Journey, Supported by Shared Care’ Webinar Series, proudly sponsored by UCB.
Wednesday 25 November
6:30pm–7:30pm AEDT
WA is coming together again
It is great to see the Western Australian myasthenia gravis (MG) community coming together again! The Myasthenia Alliance Australia (MAA) encourages you to attend if possible. Community meet-ups are a wonderful chance to connect with others who understand life with MG, share experiences and enjoy some good company. Everyone is welcome, so feel free to…
Meet Australia’s Leading MG Experts and Discover What You’ll Learn
Meet Australia’s leading neurologists, researchers and clinicians at the MAA 5th National Patient Conference. Discover the latest developments in myasthenia gravis treatments, clinical trials, diagnostic advances and patient care while learning practical strategies for everyday life with MG. Hear from experts who are helping shape the future of MG care, ask questions during the panel discussion, and gain valuable knowledge to take home. Whether you’re living with MG, supporting someone who is, or working in healthcare, this conference provides a unique opportunity to learn from some of Australia’s most respected experts while connecting with the wider MG community.
MyClad Study Now Enrolling: Open to Australians Living with Generalised Myasthenia Gravis
The MyClad Study is currently enrolling eligible Australians living with generalised myasthenia gravis (gMG). Learn more about the study, who may be eligible to participate, and how to find your nearest study centre.
Watch Now: Rare Disease Disability Toolkit Webinar with Rare Voices Australia
Watch the recording of MAA’s Rare Disease Disability Toolkit webinar with Fiona Lawton from Rare Voices Australia. Learn what it means to have a disability, how rare disease and disability can intersect, where to find support, and how the Rare Disease Disability Toolkit can help people living with Myasthenia Gravis, their families and carers navigate disability services and advocacy.
Experience a Day Designed for the MG Community
Discover what makes the MAA 5th National Patient Conference more than just another event. Held at Rydges South Bank, Brisbane, this welcoming and accessible conference combines expert presentations with meaningful opportunities to connect with others living with myasthenia gravis. Enjoy a full day of learning, discussion and community, with morning tea, lunch and afternoon tea included. Whether you’re a patient, carer, family member or health professional, you’ll leave with practical knowledge, valuable connections and a renewed sense of belonging. Join us for a conference experience designed around the needs of the MG community.
REMINDER Sydney MG Community Event | Prof Heinz Wiendl Talk.
Join MGNSW in Sydney for a rare opportunity to hear internationally respected neurologist Professor Heinz Wiendl explore the real impact of living with myasthenia gravis beyond the clinic. Register now for this special in-person event on Thursday 3nd September at 11.30 am. Gate/3 Hospital Rd, Concord NSW 2138
REMINDER Brisbane MG Community Event | Prof Heinz Wiendl Talk.
Join MGAQ in Brisbane for a rare opportunity to hear internationally respected neurologist Professor Heinz Wiendl explore the real impact of living with myasthenia gravis beyond the clinic. Register now for this special in-person event on Wed 2nd September at 3.30 pm. 171 George Street, Brisbane, QLD