The Connecticut Epilepsy Advocate was formed as an alternative organization to make more people “Aware About Epilepsy”.
As conventional as we may appear, we try to be a little different from other organizations. We have set as our goal, helping people living with Epilepsy in any way we can. Many things seen on our website may seem conventional, and might even be taken for granted. However, to the many living with Epilepsy, those same things are unconventional. How so, you ask? Well, many (but not all) people living with Epilepsy cannot work, they cannot drive and they do not know about public transportation available to them. Many cannot afford to pay for their medication. They even have trouble finding a neurologist.
The supply Medic Alert bracelets and wrist chains to help emergency personnel and the public better respond to emergencies. They’ve also connected an I.C.E form (In Case of Emergency) form so in the event of an emergency, the right people can be contacted.
Those are just a few of the many things you will find addressed on their website, and by this organization.
The Connecticut Epilepsy Advocate was founded on November 11, 2009. We encourage you to view the contents, and if you, your family or anyone you know is living with Epilepsy, we know you will find this to be a valuable resource.
Help be a part of their solution! Click the button above and join for free and start golfing at courses that supports the CT Epilepsy Advocate group.
To learn more, contact:
Connecticut Epilepsy Advocate, Inc.
20 Salem Walk
Milford, CT 06460-7132