HD Advocates

Trey Gray An Inspiration

The following Article was written March 2020 before the Pandemic.

Author Therese Crutcher-Marin

“Trey Gray is on tour right now with some of the biggest names in country music. His personal struggles with a debilitating disease are also taking up a lot of his time.

He suffers from Huntington’s Disease . He was diagnosed back in 2003. From the onset of symptoms, the life expectancy of Huntington’s is about 10 to 15 years. It’s been 17 years since Gray started having symptoms. It’s why Gray is enjoying doing what he loves and spreading awareness about his challenges.”
To watch Trey’s video, Beating the Odds of Huntington’s Disease, click here:  https://youtu.be/aJlLD-EvT1Y

Trey has four (4) children who are at risk for the mutated huntingtin gene.  He was instrumental in creating the Huntington’s Disease Foundation  another Huntington’s disease organization raising awareness, supporting families, funding research and finding a cure.

Trey wrote a blurb after reading my book, Watching Their Dance, and it appears on the back cover above Kate Miner’s blurb.  

We Can Never Lose HOPE….

I’m an Huntington’s disease advocate, Chair for the HDSA San Francisco Bay Area Affiliate, author and a blogger.  Visit my  Author/HD Advocate Website

Please donate to the nonprofit, Huntington’sDisease Society of America, and help us eradicate this incurable brain disorder.



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