Developed by Epilepsy ACT for Epilepsy Australia, this information and resource kit has been specifically designed for Aboriginal people diagnosed with epilepsy, their families and community, to assist them with basic information about epilepsy and where to find further information and assistance to help them manage their condition.
This kit it also designed for Aboriginal and Torres Strait Islander Health Workers and other health workers working with Aboriginal and Torres Strait Islander people in a range of health settings.
The resource kit consists of the following epilepsy information as Fact Sheets for Health Workers or brochures for clients:
To obtain a copy of this kit email
Epilepsy Australia National Help Line 1300 852 8653
Would you like to be included on our mailing list for The Epilepsy Report? Click subscribe below to email us.
More than 15,000 copies of a book that brings together global expertise
on SUDEP will have been distributed to epilepsy communities around the
world by the end of the 66th annual American Epilepsy Society conference.
Epilepsy Australia, in partnership with Flinders University is conducting an online survey exploring the experiences and needs of people who have been bereaved by epilepsy.
Top of Page
Privacy | Disclaimer | © Copyright Epilepsy Australia
Web Design and Development: Izilla | Web Content Management: Cognition