Michael Noyes was born without arms. But he has lived, and accomplished, far more than most people with all of their limbs. From his childhood of splitting wood on his family’s farm in a small Maine town of 500 people to playing pitcher for his local softball team to riding snowmobiles and driving Kyle around town during his visit to Maine, Michael has adapted and overcome the challenges of life with a humble and grateful attitude. 

Michael’s journey has also been one of service. He has committed his life to helping others through summer camps that help disabled children, veterans in need, adopting and fostering many children and 30 years of working for two U.S. Senators - all while typing with pencils held between his toes.

Join Kyle and Michael for an amazing conversation as he shares his inspirational and unbelievable journey.

 
You have probably never heard of Michael Noyes. After you listen to this episode, you will never forget him. 

Charlotte Jones is the Executive Vice President and Chief Brand Officer for the Dallas Cowboys. She is responsible for overseeing all of the business operations, including entertainment, community relations, cause marketing, stadium design, apparel licensing and brand marketing as it is presented to fans worldwide.

Jones has worked in the Cowboy's Executive Offices since 1989, following the purchase of the team by her father, football and business legend Jerry Jones. She has played an instrumental role in propelling the organization to where it is today, the NFL's most valuable franchise. 

Along with her many philanthropic endeavors, she currently serves as the Chairman of the National Medal of Honor Museum Foundation. The National Medal of Honor Museum is currently being built in Arlington, TX and will open Spring of 2025.

Charlotte Jones is a Stanford graduate, an advocate for women, especially those in business, and a loving mother of three children. 

https://www.dallascowboys.com/team/front-office-roster/charlotte-jones

https://mohmuseum.org/

After being diagnosed with ALS and two and a half years left to live, Lorri Carey has, now, been living life to the fullest for 19 years. Through her profound perspective and appreciation for life, Lorri shares her inspirational journey with the complex and fatal disease of ALS.

Lorri has devoted the time she has left to her podcast, I’m Dying To Tell You, where she shares the stories of people who inspire her.

ALS (Amyotrophic Lateral Sclerosis), also know as “Lou Gehrig’s disease”, is a progressive neurodegenerative disease that, over time, affects the nerve cells in the brain and spine. These nerves affect everything from breathing to eating to the usage of muscles and limbs. Currently, there is no cure for ALS.

Podcast: https://podcasts.apple.com/us/podcast/im-dying-to-tell-you/id1500657074

Website: https://imdyingtotellyoupodcast.com/

Instagram: https://www.instagram.com/imdyingtotellyoupodcast/?hl=en