![]() ![]() “He’s just really a good fan to have there, and he’s always got a smile on his face. ![]() Just seeing him up in the stands and coming out for every game and practices, it just makes my heart feel good,” Ernst said. “It’s really an inspirational aspect to my play. We just really like having him around.”įor the players, Carter’s support even inspires their game. We’ll look at Carter, and he’s dabbing and dancing, he’s all over the place and waits for us after our games, and he’s knocking on the door. “We love having Carter at our games,” said Kirsten Martin, a forward on the women’s ice hockey team. “It’s become a place where it’s big enough to be significant, but small enough to be intimate, and he has the ability to come in here and have some individual time where if Dad walks away he doesn’t have to worry about it going wrong or someone not understanding his communication.”īut when he’s not practicing for his own hockey games or skating at a stick and puck, Carter and his father are busy supporting the Lindenwood ice hockey programs at practices and games. “The rink, in general, is Carter’s safe haven,” Prewitt said. Ladd Drummond is the perfect example of this. Photo by Brad Prewitt.Īdditionally, Carter plays for the Blues Special hockey team, meaning that he and his father sometimes spend more than five days at the ice rink. Every family dynamic is one of a kind, but the relationship between a dad and his son goes unmatched (and the same can be said of a mother-son duo, too). 26, against the University of Illinois at the Wentzville Ice Arena. While he often communicates non-verbally and uses specific signs to indicate his favorite players on the ice, including tapping his right shoulder to talk about sophomore forward Caleb Ernst, after Ernst once injured his shoulder, Carter can walk, unlike many with Angelman syndrome.Ĭarter poses with the men’s ice hockey team after their game on Friday, Oct. The rare and complex neuro-genetic disorder characteristically includes developmental delays, lack of speech, seizures and walking and balancing disorders, according to the Angelman Syndrome Foundation. “It’s normal, in a life that isn’t always normal, so we love this rink, and we love these teams because it gives us a chance to be a part of something that we have a huge interest in,” Brad Prewitt said.Ĭarter is one of nearly 15,000 people living with Angelman syndrome. Carter poses happily for a picture while watching the men’s team face off against the University of Illinois Illini at the game on Oct. He returns to that same position at the end of every period, showing support even if his team is losing.įor Carter and his father, hockey is more than just a sport they enjoy watching. As the players emerge from the tunnel, Carter reaches out to touch a stick or grab a gloved hand before the skaters step onto the ice. He leans over the railing, peeking into the hallway below, with his father close beside him. At the start of every game for both the men’s and women’s ice hockey teams, 12-year-old Carter Prewitt waits for his favorite players to hit the ice. ![]()
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