Thank you for all of your support with the past walks.  Many of you know that my family has a long history with ALS. April 2022 my other older brother was diagnosed with ALS-FTD making him the 9th person in our family's tree to have this horrible disease.  Making this years walk even more important to me. Together we can fight this disease!!!  Please join my team by clicking the "Join Team" link at the top of the page and walk with us on September 28th at Sugar House Park.  With your DONATION we change the lives of people living with ALS and their care givers, while bringing about advancements in ALS research to end to ALS.  BY JOINING MY TEAM AND DONATING 90.00 OR MORE YOU WILL RECEIVE A 2024 WALK TO CURE ALS TEE SHIRT.  All donations are so appreciated.

Even if you can't join us on September 28th please use the  "Donate now" link at the top of the page to make a donation.  ALL donations stay here locally or go directly to fund research.   

Always remember to get out and walk, run, or cycle and remember those that cannot.  

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.