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SPRINTING FOR SEIZURES - FOR ANSLEY AND SCOTTIE

***Over a lifetime, 1 in 10 people will have a seizure, and one in 26 will be diagnosed with epilepsy***

Dear Friends and Family,

2020 marks our 8th year for participating in the Magnolia Run for The Epilepsy Foundation of Georgia, on behalf of Ansley and Scottie! So many of you reading this have been there, by our side, each and every year, We are so thankful for YOU!

As you are well aware, 2020 has been one heck of a ride. We are all battling the various challenges that COVID-19 has presented, in addition to the many social and political challenges we are facing as a country. Our hope is that The Magnolia Run will bring a bit of fun and happiness to our friends and family during these chaotic times...but it will look and feel a bit different this year!

To state the obvious, we cannot gather and run together, as we normally would to honor our amazing kids but we do still plan to participate and fundraise in a number of ways!

(1) It's Virtual, but we will still RUN (or walk)! What does that mean? On Saturday, November 7th -we'd like everyone to run or walk on behalf of Scottie and Ansley from wherever you are. For those that live in close vicinity, we encourage you to get a small group to run/walk together, showing our support across the country! I plan to host a group run from our neighborhood, Wateford Green, but hoping to see some small organized pods in other areas as well! November is actually Epilepsy awareness month, so this is a great way to kick it off and show your support (and the weather should be beautiful as well)!

(2) We will all wear the Magnolia Run shirts on the day of the run (v. our team specific shirts), as they will be mailed in advance of the race to all participants who raise $25 or more. You can select your size, etc. upon registration. There will also be various individual and team incentives along the way --so please tune into the EFGA social media platforms and read your emails for details on each! Rachel and I will also send some reminders along the way.

(3) Fundraising is important for the Foundation, but not necesarry to participate. We recognize that many of us have been impacted financially with the COVID situation this year, and our families would never expect you to give if faced with a financial hardship. If that's the case, please just sign up to paritipcate (no cost to do so) and join our team virtually on November 7th. The personal support is just as important for our kids!

For those of you new to this event, The Epilepsy Foundation of Georgia (EFGA) is the only health agency in Georgia dedicated to serving more than 110,000 Georgians living with active epilepsy statewide. The foundation seeks to improve the quality of life for people with epilepsy and their families through community education activities for all age levels and comprehensive set of client service programs. The foundation also reaches out to the community at large to reduce the stigma that is often attached to epilepsy and educate the public on seizure recognition and first aid. It has been a critical resource for families like ours over the years. Please consider donating, if you're able.

Much Love and Many Thanks,

Amber

 

 

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