Epilepsy Foundation of Australia

Epilepsy Foundation of Australia The Epilepsy Foundation is committed to improving the lives of people living with epilepsy.
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Social Media Terms of Service

The Epilepsy Foundation welcomes contributions to our social media accounts and encourages discussion related to epilepsy, our research, events and more. To ensure a safe environment for all members of our community, we ask users to abide by these Terms of Service and reserve the right to remove any content we deem inappropriate. When posting, please respect the view

s of other users and be aware that our accounts are viewed by minors (people under the age of 18). Accordingly, posts and contributions should be suitable for individuals of all ages. All material posted by users must comply with the relevant service’s Terms of Use. In addition, users may not post any material that:

• Is abusive, threatening, discriminatory or defamatory
• Is unlawful, fraudulent, misleading or malicious
• Infringes on the intellectual property rights of others
• Is offensive, obscene or otherwise inappropriate
• Is entirely off-topic or has been excessively reposted by a user
• Advertises or offers to sell any goods or services, contains spam or any other unsolicited commercial messages

We reserve the right, in our absolute discretion, to remove, untag and/or report any posts, including those that violate these Terms of Service. Users who breach these Terms of Service may be blocked from contributing. The Foundation accepts no liability for any loss arising from or in connection with users being blocked from the relevant service or the deletion of a user’s content. Comments and posts on our social media accounts made by those outside the organisation do not necessarily reflect the opinions of the Epilepsy Foundation, its employees or affiliates. The Epilepsy Foundation does not endorse this material and is not responsible for its accuracy. Please note that we cannot guarantee the privacy or security of conversations made through social media messaging apps or email. While we do our best to ensure the integrity of these platforms, if you have any concerns, please contact the National Epilepsy Support Service on 1300 761 487. The collection of personal information by the Epilepsy Foundation is governed by the Privacy and Data Protection Act 2014 (Vic) and Health Records Act 2000 (Vic) (together, Privacy Laws). The Epilepsy Foundation is committed to protecting your privacy and processing your personal information fairly and lawfully in compliance with the Privacy Laws. Please refer to our Privacy Policy for information about how we handle personal information. The Epilepsy Foundation reserves the right to update these Terms of Service from time to time.

31/08/2026

Last week, Member of Parliament John Pesutto made a statement in Victorian Parliament about epilepsy and the Epilepsy Foundation, encouraging Victorians to support the important work we do 💬

John is passionate about raising awareness of epilepsy amongst our community and ensuring those living with the condition can access the care they need.

We extend our sincerest thanks to John for his words of support and advocacy for people living with epilepsy 💜

Learn more about epilepsy and how you can access support at www.epilepsyfoundation.org.au

28/08/2026

North Melbourne star, Luke McDonald, is back supporting the Epilepsy Foundation in Walk for Epilepsy 2026, with a very personal reason for getting behind the cause.

Luke’s wife, Brooklyn, was diagnosed with epilepsy, giving Luke and his family firsthand experience of the impact epilepsy can have on the people living with it - and those around them.

Luke has supported Walk for Epilepsy before, including bringing together a team of Roos for our Treadmill Challenge in 2025.

This October, Luke will be Moving for the Moments that matter and standing alongside the 1 in 25 Australians diagnosed with epilepsy in their lifetime.

Join Luke and register at https://www.walkforepilepsy.org.au/04667E

27/08/2026

As a neurologist and researcher specialising in epilepsy, Dr Emma Foster spends her days working to better understand epilepsy, improve treatment and help people living with seizures 🧠

She’s also no stranger to the Epilepsy Foundation community, having previously supported us as an ambassador and used her expertise and voice to help raise awareness of epilepsy 💜

Now, Emma is back - ready to Move for the Moments that matter and stand alongside the 1 in 25 Australians diagnosed with epilepsy in their lifetime 👟

Because better understanding, better care and better support can make a real difference.

Join Dr Foster and register at https://www.walkforepilepsy.org.au/04667E

WE'RE HIRING 💜 We’re looking for a compassionate and motivated Epilepsy Advisor to join our Comprehensive Support Servic...
26/08/2026

WE'RE HIRING 💜 We’re looking for a compassionate and motivated Epilepsy Advisor to join our Comprehensive Support Services team.

In this rewarding role, you’ll work directly with people living with epilepsy and their families, providing practical support, education and guidance to help them navigate challenges, build self-management skills and participate more fully in everyday life.

No two days will look the same. You’ll support clients, contribute to our information line, facilitate workshops and deliver epilepsy education across schools, workplaces and families.

💼 Epilepsy Advisor
💜 Meaningful work with real community impact
🤝 Supportive and knowledgeable team
📚 Specialist learning and professional development
🏡 Flexible work options
💰 Salary packaging benefits

If you’re passionate about helping people thrive and want your professional skills to make a genuine difference, we’d love to hear from you.

👉 Learn more about the position and apply: https://bit.ly/4qWddv3
✉️ Contact our Practice Leader with any questions about the position: [email protected]

25/08/2026

For Brett Ratten, this is more than just a walk 👟 It’s personal 💜

An AFL legend and devoted dad, Brett knows firsthand the impact epilepsy can have on a family. His daughter Tilly was experiencing up to 30 seizures a day before she was diagnosed with epilepsy.

Since then, Brett has used his voice to help raise awareness, break down misconceptions and support others living with epilepsy and their families.

Now, he’s back supporting the Epilepsy Foundation in Walk for Epilepsy 2026 and helping us Move for the Moments that matter 🚶🏻

Because behind every statistic is a person, a family and a story.

Join Brett and register at https://www.walkforepilepsy.org.au/04667E

Every student deserves to be part of the action 🧑‍🎓💜Camps. Excursions. Sport. School trips. Extracurriculars.Having epil...
24/08/2026

Every student deserves to be part of the action 🧑‍🎓💜

Camps. Excursions. Sport. School trips. Extracurriculars.

Having epilepsy shouldn’t mean sitting on the sidelines.

At the Victorian School Nurses Association (VSNA) conference on Saturday, our team joined school nurses from across Victoria to talk about what it takes to create safe, inclusive school environments where students with epilepsy can participate fully.

Our Epilepsy Lead Educator, Matt, was invited to present and share his knowledge, as well as some of the work we do at the Epilepsy Foundation to support children and schools.

The key? Planning, preparation and knowing the student.

💬 Instead of asking “Can they participate?”, let’s ask:

💬 “What do we need to do so they can?”

A big thank you to VSNA for having us, and to the incredible school nurses who work every day to make participation possible for students with epilepsy.

Because epilepsy might need a plan - but it shouldn’t need to limit the plan.

🔗 Learn more about how we can support your school and register for one of our training courses: https://bit.ly/4la94Pg
📞 (03) 8809 0695 | 📧 [email protected]

Epilepsy is part of your story. But it isn’t the whole story 📖💜For some people, epilepsy can feel like it takes up a lot...
19/08/2026

Epilepsy is part of your story. But it isn’t the whole story 📖💜

For some people, epilepsy can feel like it takes up a lot of space - in plans, conversations, decisions and everyday life.

But there is so much more to you than epilepsy.

Your dreams. Your relationships. Your achievements. Your laughter. The little moments that make life yours.

Whatever chapter you’re in right now, remember: you’re still writing the story 📝

To everyone living with epilepsy - we’re with you 💜

For further information around epilepsy, please visit www.epilepsyfoundation.org.au or contact the National Epilepsy Support Service on 1300 761 487 or [email protected]
Face-to-face meetings are by appointment only.

18/08/2026

The 1 in 25 Challenge is back 👟

100km in 25 days - walk, run or ride your way through it at your own pace. A challenge designed to keep you moving and raise awareness for the 1 in 25 Australians who are diagnosed with epilepsy in their lifetime.

And if you’re ready to take it further... Introducing the 1 in 25 Legends Challenge 💪

1,000km in 25 days. Built for those who want to push distance, discipline and determination even further. Do you dare step it up a notch?

However you take part, every kilometre and every moment of your journey helps support people living with epilepsy and their families 💜

This is your challenge. Your pace. Your impact.

Register at https://www.walkforepilepsy.org.au/04667E

Thank you to John Pesutto for visiting our office to learn more about our work supporting people living with epilepsy 💜Y...
18/08/2026

Thank you to John Pesutto for visiting our office to learn more about our work supporting people living with epilepsy 💜

Your passion for creating change and bringing epilepsy into the conversation is truly appreciated.

Address

Level 1, Suite 3/210 Canterbury Road, Canterbury
Melbourne, VIC
3126

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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