Dear family and friends,
I'm reaching out to you to help me raise money to defeat ALS. As you know, Jake recently married Taylor Capener on April 10th. It was such a joyous occasion, especially since Taylor's dad, Art, was able to attend and escort her down the aisle.

Unfortunately, Art was diagnosed with ALS in September 2020 and passed away two weeks after the wedding on April 23rd.

Jake and Taylor spent 5 months caring for Art and wouldn't have wanted to be anywhere else. Their devotion to him and his care was beyond selfless.

Art's ALS was 'familial'; his father and brother also succumbed to this devastating disease which currently has no cure. There is a possibility that Taylor is a carrier too. I am determined to do everything I can to bring awareness to ALS and to contribute to finding a cure.

I will be walking in the Central Oregon ALS walk on May 15th.  Please pray for Art and the family he left behind on the 15th and if you can, help me raise money for research to eradicate this awful disease.

Thank you,
Cathy

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 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.

With your help, we will be able to make a difference in the lives of people affected by this disease.