Connecticut Epilepsy Advocate Foundation

The Connecticut Epilepsy Advocate Foundation is a nonprofit organization dedicated to raising awareness about epilepsy, providing support, and advocating for individuals affected by the condition. Established as an alternative organization, its mission is to make more people aware about epilepsy and assist those living with it across the United States and locally in all 169 cities and towns in Connecticut.

Mission and Activities

The foundation offers various services aimed at enhancing the quality of life for people with epilepsy. Key initiatives include:

• Awareness and Education: Efforts to increase public understanding of epilepsy and its impact.
• Support Groups: The foundation has established support groups in several locations across Connecticut, with plans to expand further. Volunteers are encouraged to participate, and training is provided for those who wish to lead groups.
• Assistance Programs: The organization helps individuals obtain Medic Alert bracelets, which are crucial for emergency situations. It also provides financial assistance for prescriptions and groceries when needed.
• Advocacy: The foundation advocates for students with special needs and veterans with epilepsy-related disorders, addressing issues such as PTSD and access to healthcare.

Recognition and Outreach

As a recognized 501(c)(3) nonprofit organization, the Connecticut Epilepsy Advocate Foundation has been featured in various media outlets. It leverages platforms like television and newspapers to reach a broader audience and raise awareness about epilepsy.

Founding and History

The foundation was founded on November 11, 2009, with the goal of filling gaps in support and awareness for epilepsy in communities across the U.S. and Connecticut. Its approach is to be accessible and proactive in addressing the unique challenges faced by individuals with epilepsy.