Why I'm Walking ❤

On November 7th, I'll be participating in the 2026 Walk to End ALS in Scottsdale. I'm walking for Leah, the mother of my dear friend, and for a family that means so much to me.

Leah was officially diagnosed with ALS in February of this year. Sadly, this isn't the first time her family has faced this devastating disease. Leah's mother also had ALS.

Leah is an incredibly strong woman who loves her family deeply. She’s a mother of four and grandmother of five.  Now, the very people she has spent her life loving and caring for are rallying around her as she faces this unimaginable journey. We'll walk to honor her strength, support her family, and raise awareness for a disease that desperately needs a cure.

If you're able, please consider making a donation or joining us for the walk. Every contribution, no matter the size, makes a difference.

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, and presently there is no known cause or 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. 

But, we can’t stop now! The key to a cure starts with all of US. Please consider walking with me or making a donation to my team. With your help, we will be able to make a difference in the lives of people affected by this disease.