Thank you for visiting our page! Many of you know that Jesse's mom, Sue, was diagnosed with ALS in 2024. We are joining "Walk to End ALS" in her honor hosted at Salt River Fields on November 8, 2025. We hope that you will join us in supporting Sue and all of those affected by ALS. We want to spread awareness of the urgency to find treatments and a cure. By donating and helping us reach our ALS Walk fundraising goal ($1000), you will be joining in the fight to end ALS. 

WHY WE NEED YOUR HELP? 

Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.? 

That?s why we?re participating in the Walk to End ALS. To bring hope. To raise awareness. To provide resources and services to families free of charge. To help unlock the mystery of ALS and find the key to treatments a cure. Please join us.  

ABOUT 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. Presently there is no known cause of the disease, yet it still costs loved ones an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to provide help and hope today! 

Thank you for your support,

Jesse, Trisha, Brock & Brinley Wright