As many of you know, my wonderful daughter-in-law, Melissa Korn was diagnosed with ALS just over 2 years ago. Words cannot describe either the heartbreak this brought on, nor the absolute warrior spirit Melissa and her family (Her husband, Garrett, and her two boys Theo, 4 and Weston, 2) have embraced in fighting this debilitating  condition. They truly are an inspiration. 

As many of you also know, public funding for treatment, research, and other aid has almost completely dried up in the wake of Doge and the current administration's policies. That's why we are asking you to all help out, if you can, to the extent that you can. I understand if you can't, times are tough, but please think about it, and click that "Donate" button. 

And, if you're feeling frisky, come on down to the Field formerly known as Turner (now Center Parc  Stadium) on September 20th, and come on the walk with Team Melissa!!!

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.