Our upcoming webinar with Rare Voices Australia is just a few days away, and this is your last chance to register.
If you’ve been thinking about attending, now is the perfect time to secure your place for this valuable educational session designed specifically for people living with Myasthenia Gravis, along with their families and carers.
Presented by Fiona Lawton, Disability Advocacy Manager for Rare Voices Australia, this webinar will explore how a rare disease can also become a disability and what that means when accessing disability supports and services.
The session will cover:
- Understanding rare disease and disability
- The Rare Disease Disability Toolkit
- Disability advocacy and self-advocacy
- The NDIS and supports beyond the NDIS
- Live questions from attendees
If you’ve ever wondered whether you may be eligible for additional supports, or simply want to better understand the disability landscape, this webinar offers practical information that could help you navigate your options with greater confidence.
Webinar Details
Tuesday 28 July 2026
12:30pm to 1:30pm AEST
- NSW, VIC, QLD, TAS, ACT: 12:30pm to 1:30pm
- SA, NT: 12:00pm to 1:00pm
- WA: 10:30am to 11:30am
If you are unable to attend on the day, don’t worry. Everyone who registers will still be able to access the webinar recording afterwards via the MAA website.
Registrations close soon, so don’t miss this opportunity.
https://rumi-live.zoom.us/webinar/register/WN_sGU-mCfbTMWWadz69_FYVQ#/registration