We’re excited to introduce MG Vic, Victoria’s association, to support people across the state living with Myasthenia Gravis.

MG Vic will amplify the voices of patients, families and carers through awareness and education.  

We will connect the MG community and beyond, with local events in your area, as well as raising awareness. We are also planning educational forums in person and online. 

Right now, we’re looking for people to join our committee. If you’re interested, please tell us about your experience with MG and how you believe you could assist plus your work background skills – even a CV if you like.

Submissions are due on Sunday 23.11.2025. Please send to info@mgvic.org

So you can stay up to date on everything, like the upcoming launch of MG Vic’s new website, as well as our Morning Teas, where you’ll get the chance to tell us what you want MG Vic to be about, please follow our Facebook page.

Membership will be available on the website very soon.

For further information contact Catherine Bergin – President MG Vic 0418 563 557