It's been 8 years since Leo was diagnosed with ALS. He's been gone five and a half years now. On Sept. 27, I'll be participating in Walk ALS Utah to support those affected by ALS and to spread awareness of the urgency to find treatments and a cure, and to raise funds to support those affected by ALS.

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.

By walking I'm aiming to help 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.

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.  

Thank you for helping me reach my Walk ALS Utah fundraising goal.  ~Carol

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