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Amy Wilson

Amy Wilson

His faith is sustaining and watching him battle this disease is teaching my boys endurance and perseverance. The photo is my dad! To me he is a Superhero. He is battling Bulbar ALS and has not eaten or drank anything in over a year and nonverbal. He fights everyday...
Alicia Hartsell

Alicia Hartsell

Our greatest fear lived out that day. We lost our precious Dad August 2022 to this cruel disease. He was officially diagnosed just 6 months prior, but his journey began a few years before. It was March 2019 and he began to slur his words then lose his voice… we were...

Kaitlin Wilcox

Throughout my father’s entire journey- struggle with diagnosis, denial, anger- my Mom’s health took a significant decline. We have no family history of ALS. In 2018 my father started experiencing a strange set of symptoms such as shortness of breath and...
James Clingman

James Clingman

Let’s hope and pray ALS will one day soon get the respect it certainly deserves, in the forms of financial support for its victims, legislative support, FDA approval, research grants, and education. ALS is the Rodney Dangerfield of diseases. It gets no respect....