POV: My Life with a Rare Muscle Disorder | PEOPLE

"I really wish that there was a way for everyone to spend just one day of their life in a wheelchair," says Kevin Sullivan who was born with Arthrogryposis Multiplex Congenita (AMC), a rare muscle and joint disorder that limits mobility in his arms and legs. The 34-year-old motivational speaker and disability rights advocate invites viewers to follow his full day — from morning to night — to see the challenges he faces and the creative ways he adapts. With the help of three caregivers and assistive technology, Kevin moves through his routines with patience and determination, whether it's eating with an adaptive feeding device, playing his favorite sport of baseball or using the restroom: “You’ve got to be comfortable with being uncomfortable," he reflects. Through his quiet strength and humor, Kevin shows how much thought and effort go into maintaining independence and keeps a positive attitude through it all: "I'm forced to stop and smell the roses." Keep up with Kevin's journey here: Instagram: https://www.instagram.com/kevsullytalks TikTok: https://www.tiktok.com/@kevsullytalks YouTube: https://www.youtube.com/@kevsullytalks Facebook: https://facebook.com/kevsullytalks LinkedIn: https://linkedin.com/in/kevsullytalks Subscribe to People ►► http://bit.ly/SubscribetoPeople *CONNECT* Web: 💻 https://people.com Facebook: http://facebook.com/peoplemag Instagram: https://www.instagram.com/people/ TikTok: https://www.tiktok.com/@people PEOPLE App: 📱 https://bit.ly/3H0bthA *PEOPLE* remains the trusted authority at the center of pop culture. The PEOPLE brand features a unique mix of breaking entertainment news, exclusive photos, video, unparalleled access to the red carpet, celebrities, and in-depth reporting on the most compelling newsmakers of our time. POV: My Life with a Rare Muscle Disorder | PEOPLE https://www.youtube.com/user/people