Our beloved Art was hoping to see a cure for ALS during his lifetime. His desire was to be part of all clinical trials that were available to him. Although he did not get to see a cure, he is whole, healed and free now in Heaven! For those of us who remain, perhaps we can help see this cure happen as we march in his honor and memory. Our deepest prayer is for no one else to ever endure this devastating disease again.
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 we are 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.
We have chosen to make this walk an annual tradition in our family. We would love it if you might join us as part of Art's Amazing Army and walk with us along the Columbia River. With your help, we will be able to make a difference in the lives of people affected by this disease. Art would be so proud!