We are walking this year in honor of my incredible Aunt Diane, who faced ALS with grit and courage, all with a smile on her face. We miss her more than words but we hope to honor her memory by raising funds for resources to help those affected by ALS and to support new and ongoing ALS research. Join us on September 22nd to walk or donate to our team!
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 joining me or making a donation. With your help, we will be able to make a difference in the lives of people affected by this disease.
