Dana Fichera

Aug 10, 2024

It is a horrible horrible disease to watch someone go through. ALS is a horrible and debilitating disease. I lost my grandmother to it. To watch someone that has their brain 100% intact and everything else just go it’s so sad. It is a horrible horrible disease to...

Joyce Williamson

Aug 10, 2024

Our decision was to live with ALS not die with it. My husband was diagnosed October 26, 2018 and passed September 27, 2020. I thank God that he did not have to suffer longer with this disease. It all started after a hip replacement on his right hip in Feb 2018. A...

Minna Dillard-Brown

Aug 10, 2024

My Clifford was diagnosed 5 months before he left us on Valentine’s day 2016. My Clifford was diagnosed 5 months before he left us on Valentine’s day 2016. This is why I advocate for the ALS community. I’ll be in Atlanta with the Braves June 2...

Andrea Denhart

Aug 10, 2024

Jeff was the person who smiled at everyone. His greatest joy was making others happy. He had a gift of making others feel loved. He made our world a better place. My big brother, Jeff was my best friend. He has played baseball and loved baseball all of his life. Our...

Mandy Henry

Aug 10, 2024

Prior to my Dad being diagnosed with ALS in May 2017, the only thing I knew about ALS was it was named after a famous Yankee baseball player Two different stories from two daughters who had to watch their Dad die of this horrific disease: my sister, who was our Dad’s...