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. 

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. We have witnessed first-hand the toll ALS has taken on Sue's body and her daily living. While just a year ago she was independent with self-care and walking, today she requires assistance with mobility and will soon need a speech device to assist with her communication. This has been heartbreaking for Sue and her loved ones.

That is why we are walking. To change the statistics. To bring help and hope to Sue and all of those living with the disease. To support the caregivers, who help their loved one fight this disease. To ensure that there is a cure.  

The past few 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. 

We cannot stop now, the key to a cure starts with all of us! Please consider walking with our family or making a donation to our team. With your help, we will be able to make a difference in the lives of people affected by this disease.

Sincerely,

Jesse, Trisha, Brock & Brinley Wright