When someone you love gets diagnosed with ALS, the first thing you ask is what can I do to help? For many people like me, the answer is to participate in Walk ALS Georgia, which raises awareness and money to support all Georgians living with ALS.  

Amyotrophic lateral sclerosis (ALS) is a progressive neuromuscular disease that slowly robs a person of the ability to walk, speak, swallow, and breathe. It can strike anyone and, although there has been a lot of advancements in ALS research, we still don’t know what causes it. An ALS diagnosis is fatal because there is no cure.

In 2022, I was diagnosed with ALS. Since then, my family and I have been facing this journey together—embracing each day with courage, love, and determination. We strive to live life to the fullest and smile through it all.
My greatest hope is to create lasting memories for Ella—moments she’ll carry with her forever..

We are going to be out of town on the day of the walk, but we invite you to donate and walk virtually with us.  Every donation—no matter the size—helps provide critical care and life-enhancing equipment for Georgians living with ALS. Our hope is that one day, when Georgians hear the words, “You have ALS,” it will no longer mean that they likely will die within two to five years. I am walking so that Georgians living with ALS today know that they are not alone. I’m walking to assure that when they need help, they will be able to get it from ALS United of Georgia. I am walking to give them hope. 

You may not know anyone with ALS, but you do know me, and I am asking for your support. Will you please consider joining me to make strides in the fight against ALS? You can join our team or make a gift to support our team. Either way, with your help, we can enhance the lives of people living with ALS, every day until we find a cure.