My friend (Kathryn Dieck-Walton) and colleague when I was teaching was diagnosed with a form of ALS.  The affects of ALS are dramatic, painful and life changing in so many ways.  Instead of immersing herself in self pity she is a bright light to all....never complaining.  Please support me as a team member when Kathryn uses special equipment to sit ski In Breckenridge the end of March.  More information is below.

Thank you for helping me reach my Ski ALS fundraising goal! Ski ALS raises funds to support those affected by ALS and to spread awareness of the urgency to find treatments and a cure.

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 skiing. 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 three 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 skiing 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.