This is for my husband Donald Caperton.  We noticed first symptoms in March 2022 and he was diagnosed in July 2022. He sadly passed away in November 2022.  His ALS progressed rapidly and praying that someday soon there will be a cure for this devastating disease.  

Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of a person with ALS averages 2 to 5 years from the time of diagnosis. ALS can strike anyone, and presently there is no known cause or cure.

That’s why I’m walking. To change the statistics. To bring help and hope to those living with the disease. To ensure that no one ever hears the words: “You Have ALS” again.

The past two years have brought incredible advancements in ALS research, expanded access to care for people living with ALS, and enabled legislation that impacts the quality of life of people with ALS and their families.

But, we can’t stop now. The key to a cure begins with you.

Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.