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Colts RB Nyheim Hines named national spokesperson for MDA

It's personal for the 24-year-old, who lost his grandmother to the disease and watches his mother and uncle battle it daily.
Credit: AP
Indianapolis Colts running back Nyheim Hines catches during pregame of an NFL football game against the Detroit Lions, Sunday, Nov. 1, 2020, in Detroit. (AP Photo/Duane Burleson)

INDIANAPOLIS — We’ve all seen what Indianapolis Colts running back Nyheim Hines can do on the field, from his shifty moves to those acrobatic performances in the end zone. As much as Hines gives to the game, he’s now using it to give back and shine a light on an important cause.

“Things were planned a long time ago, when I first told my agent, ‘This is something that’s going to be important to me. I told him one day, hopefully I make a lot of plays and become something of myself, I knew for sure I would use my platform to give back in any type of way I could to muscular dystrophy, for MDA," Hines said.

If you looked at Hines’ feet during the December game when he scored against the Texans, you may have noticed the custom black and green cleats with the words "Muscular Dystrophy Association" on the side. Every year since entering the league, Hines has chosen to highlight MDA for My Cause, My Cleats.

Credit: AP Photo/David J. Phillip
Indianapolis Colts running back Nyheim Hines (21) celebrates his touchdown against the Houston Texans during the first half of an NFL football game Sunday, Dec. 6, 2020, in Houston. (AP Photo/David J. Phillip)

It’s personal for the 24-year-old. He lost his grandmother to muscular dystrophy and he watches his mom and uncle fight the disease daily.

“I’ve actually just sat there about to cry," said Hines. "It’s hard to watch one of your loved ones fight every day. But then as I cry, I kind of stiffen my lip up a little bit and hold up my head like a nosebleed and I keep pushing because I know my mom and my grandmother and my uncle wouldn’t want me to cry. They would want me to do exactly what I’m doing now, fight for not only muscular dystrophy, but ALS and all the other 33 neuromuscular diseases that occur."

This year, Hines is taking that fight to a new level. He’s been named the 2021 national spokesperson for the Muscular Dystrophy Association. It’s ideal role for him.

“I’ve seen people talk about breast cancer, all sorts of things, but nobody ever said anything about muscular dystrophy. It’s kind of cool that I can be that person. I’m happy that it’s me," he said.

Through this new partnership, Hines wants to keep pushing neuromuscular diseases to the forefront.

“Just raise awareness, raise money for it,” Hines said. "I’m going to donate personally, and if people don’t give money, that’s fine. Just know what it is. There might be somebody around that is affected. If you just go over there and help them every day, that’s fine. And help people know what it is and help others."