Epilepsy Association of Tasmania aims to improve the quality of life and community participation for those Tasmanians with and affected by epilepsy.
The Epilepsy Association of Tasmania was formed by a group of concerned parents in 1975 to provide support and information to all Tasmanians affected by epilepsy. The Association has worked for over 30 years to inform the people of this state about epilepsy and appropriate care for people who experience seizures. Working with limited resources and supported by volunteers, the Association has always aimed to provide services of the highest quality.
The Epilepsy Association of Tasmania also plays a significant role in facilitating communication between the various agencies dealing with epilepsy management and care. It is determined to keep the community generally up to date on these issues. From this position, it is well placed to provide an informed overview of the topic. We have assisted government by liaising with the relevant departments to ensure that policy reflects modern medical advances as well as the perspective of consumer needs. With the increasing awareness of epilepsy related deaths, our role is more important then ever.
