The Epilepsy Foundation of Georgia is a non-profit organization dedicated to helping Georgians with epilepsy/seizure disorders. Based in Atlanta, the Foundation focuses on: educating the professional and general community about epilepsy through annual symposiums and programs held throughout the state; providing outreach through a statewide network of support groups; and assisting in quality of life issues through specialty camps for children/adults and medical referrals and advocacy on behalf of all Georgians living with epilepsy.
Epilepsy Foundation of Georgia
6065 Roswell Road #515
Atlanta, GA 30328-4011
Phone: (404) 527-7155 / (800) 527-7105

During the first six months of the 2007-2008 fiscal year the Epilepsy Foundation of Georgia provided

80 educational in-services reaching 7,203 people in 72 counties
Information and referral to 1,806 people
Summer camp scholarships for 52 children and adults w/seizures
Emergency medication assistance for 53 persons
Very successful educational seminars in Dalton and Atlanta
Certification of two more school districts in the Managing You Student With Seizures school nurse training

These programs were made possible by the following accomplishments

The Taste of Love dinner raising a net of $226,000
An successful Annual Campaign, raising $75,000
The Magnolia Run raising a net of $14,000
The renewal of our UCB corporate sponsorship for an additional three years
Transfer of the Endowment Fund to the full control of the Georgia Affiliate
Increased exposure through two Wine and Dine events and Advocacy activities

This website is filled with information and tools designed to help you "seize control." The tabs/links to the right and at the top of this page will allow you to explore specific topics and programs in more depth. We share a common goal with you: to improve the quality of life for persons with epilepsy/seizure disorders.

The information contained in this website is provided for information only. Such information does not constitute medical advice, and should not be relied upon as such. The Epilepsy Foundation of Georgia (EFGA) does not engage in the practice of medicine. EFGA, under no circumstances, recommends particular treatments for specific individuals, and in all cases, recommends that you consult with your physician before pursuing any course of treatment.

Upcoming Events:

June 15-21 - Camp Lakewood
June 15-20, 22-27 - Camp Big Heart
2008 Summer Camps
Swimming, arts and crafts, campfires, seeing old friends and making new friends. (see details)
Saturday, June 28; Registration begins at 6:30am
Perimeter Mall Parking Lot
4400 Ashford Dunwoody Road
Lace up your running shoes and get ready for the 25th Annual Magnolia Run and Walk to benefit the Epilepsy Foundation of Georgia. Registration opens at 6:30am with the 4 mile run, at 7:30pm and the 1 mile walk/run starting at 8:30am.
All participants will receive a Magnolia Run T-shirt! As always, there will be wonderful food available to everyone at the finish line. Awards will also be presented to winners in multiple age groups.
Tickets: To avoid the lines (and get a little extra sleep on Saturday morning!) you can pre-register online at www.active.com. Pre-registration is $20 and day of registration is $25 with ages 12 and under only $15. For more information on the 2008 Magnolia Run email Pam Murphy or call (800) 527-7105.

July 16, 2008 - Epilepsy Art Contest
Now, people with epilepsy can show their creative talents by participating in the 2008 Expressions of Courage Art Contest. The contest is sponsored by Ortho-McNeil Neurologics, with anyone diagnosed with epilepsy eligible to submit artwork for the contest. Artwork may be done in ink, pencil, crayon, or paint on paper or board. Participants must complete the contest entry form and submit it with their artwork. Deadline for submission of artwork is July 16, 2008. (see details)

November 1, 2008 Symposium Theme Selected
The 2008 Epilepsy, Speak Up, Speak Out, will focus on advocacy, and the many ways that you and your loved ones can become effective Epilepsy Advocates. One workshop you definitely don’t want to miss will be Medical Advocacy, which will explore ways you can become a more informed patient advocate in dealing with your physician or pharmacist. (see details)

What's New:

2008 Taste of Love Annual Gala
Sat February 9 - The Epilepsy Foundation of Georgia hosted its annual gala Taste of Love, an elegant black tie event held annually at the Ritz-Carlton, Atlanta. This year, Taste of Love raised a record breaking $260,000. Proceeds from Taste of Love are directed towards epilepsy research, education, advocacy, services, camperships and a medication fund. (learn more...)
UCB, Inc. (The Epilepsy Company) provides 30 one-time scholarships for people living with epilepsy or family members/caregivers who demonstrate academic and personal achievement. (learn more...)
Combined Federal Campaign
Do you work for the State or Federal Government in any way? We are getting into the time period when you will be asked by your employer representative to give to the Combined Federal Campaign. This year you will use the code number 45051 whether you live in Metro Atlanta or anywhere in the State of Georgia. No matter which division of the Federal Government or any state in the United States that you might work for, you can use the number 45051 and your contribution will come to the Epilepsy Foundation of Georgia. Please support our work in the State of Georgia.
Volunteer
It's the people of the Epilepsy Foundation of Georgia that make it work. We are led by a very active Board of Directors and also receive guidance from the members of our Professional Advisory Board. If you'd like to volunteer time helping us provide services and information on epilepsy or helping us with grant writing, obtaining corporate sponsorships, or with other fundraising projects, please let us know!
Donate
The Epilepsy Foundation of Georgia is committed to being a good steward of the gifts we receive by sensibly managing your donation. Please

join us in our efforts to help the thousands of people in Georgia who have epilepsy live a normal life.
Medicare for Persons With Epilepsy
The new changes to the Medicare prescription drug program can present some very difficult decision for persons with epilepsy. (details)