2025 Walk ALS Georgia: Mr. Ethan Hostetler

The recent diagnosis of ALS for my wife, Laurie, has profoundly affected not just her, but our entire family and community. As a mother and stepmother to Ryan, Cameron, Liam and Holden, Laurie has always been the heart of our household. She radiates with love, laughter, and warmth. Her quick wit and ability to bring people together have created countless cherished memories. Now, as we navigate this challenging journey, we find ourselves facing an emotional landscape that is both overwhelming and transformative.

Our boys, tender-hearted and resilient, are grappling with a mix of confusion, sadness, and an emerging sense of strength. They are learning to confront their feelings and support each other in ways they never anticipated. Each day presents a new challenge, but we are committed to fostering an environment where they can express their emotions freely and find solace in one another. The impact of this diagnosis extends beyond our immediate family; it ripples through our friends and extended family, who are equally affected by Laurie’s diagnosis. They have always looked to her for guidance and joy, and now they find themselves rallying around us, offering love and support in ways that are both heartwarming and humbling.

We believe that raising awareness about ALS is crucial—not just for those diagnosed, but for everyone connected to them. It’s important for people to understand the emotional struggles faced by families navigating this disease, as well as the unseen battles those with ALS endure. By participating in Walk ALS Georgia, we hope to unite our community and shed light on the realities of living with ALS. This event is more than just a walk; it is a chance to honor Laurie and all those affected by ALS, while fostering understanding and compassion within our community.

Together, we can amplify our voices and share our story, ensuring that the struggles and triumphs of those living with ALS are recognized and addressed. We invite everyone to join us in this mission, to raise awareness, and to support one another through the challenges that lie ahead.

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 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.

I am walking so 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.