I walk. . . because I can. I walk. . . for those that can't. I walk. . . to create awareness and one day find a cure for ALS. Not only do I have the privilege as serving as the Executive Director of The ALS Association of Georgia, I have the honor to know so many great people with this dreaded disease. Heartbreaking of all, is that there is no cure and there are no survivors. My hope is that those I meet and become friends with, will be lifelong friends, not short-time friends. Please join me by supporting my efforts, either by walking on October 17th (wherever you may be) or by making a donation to my walk team.
The Walk to Defeat ALS® is an exciting opportunity for us to work together to support those affected by Amyotrophic Lateral Sclerosis (ALS) and to spread awareness of the urgency to find treatments and a cure.
Due to COVID-19, this year's Walk will be a little different. We are saying "Walk Your Way!" So, you can join me on 10/17 and walk in my neighborhood or you can walk wherever you are! With your help, we will be able to make a difference in the lives of people affected by this disease. I invite you to join me and our team to get involved and walk, fundraise, or donate to make a difference for those living with ALS!
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Why We Need Your Help
Often referred to as Lou Gehrig's Disease, amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of an ALS patient averages 2 to 5 years from the time of diagnosis.
Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
This crippling disease can strike anyone. Presently there is no known cause of the disease yet it still costs loved ones an average of $200,000 a year to provide the care ALS patients need. Help make a difference and donate or join a walk today.
