Of courage, basketball and conquering the obstacles in his way: The Justin Williams story
OCOEE, Florida – Justin Williams was 8 when he underwent surgery to allow more room for his brain to grow. For two months he wore a halo brace and a plate on the roof of his mouth to push the bones in his face forward one agonizing millimeter at a time.
At one point, Justin told his dad, John, that he’d rather die than live through that again.
“At the time, I was probably exaggerating,” Justin said, “but it was the worst eight weeks of my life.”
Justin, 18, was born with Apert syndrome, a rare condition where the joints in a baby’s head, face, feet, and hands close while in the womb. He’s undergone surgeries on his feet, hands, face and head – 15 in all. The first was when he was 9 months old. He learned to walk with both feet and hands in casts.
While Justin has endured some difficult moments in his life, he will be the last to say he’s had a difficult life.
“I’ve gone through a lot,” he said, “and it hasn’t affected me.”
Justin grew up on Ocoee, just a short walk from his family’s blueberry farm, where he helps direct the parking during picking season.
He graduated in the spring from Foundation Academy in nearby Winter Garden. He attended the private Christian school since pre-K on a McKay Scholarship for Students with Disabilities (now the Family Empowerment Scholarship for Students with Unique Abilities, administered by Step Up For Students). He begins classes at Valencia College in August.
Justin was one of the most popular students on campus and certainly the most popular player on the basketball team. His classmates would fill the stands and chant his name until Coach Nathaniel Hughes sent Justin into the game. Then Justin would reward his fans by hitting long-range 3-point shots.
“It’s so much fun to watch him play,” Justin’s mom, Stacy, said. “It blows me away, the support of all the people.”
Justin’s efforts on the court led to his receiving the Jersey Mike's Naismith High School Basketball Courage Award. The honor is given annually to a male and female high school basketball player who has “gone above and beyond throughout the basketball season and has demonstrated courage in their approach to their team, school, and community.”
“I don’t think I’ve ever heard him complain, say something was too hard or he couldn’t do it,” Hughes said. “I never heard that, and he has way more reason to complain than I do.”
HE CAN DO IT!
“What is a normal life?” John Williams asked on a recent afternoon at the blueberry farm.
While pregnant with Justin, Stacy said she wondered what type of life he would lead. Would he excel in sports? In school? What would his interests be? His talents? What would he choose for a career?
Justin was born in September 2003 with a craniofacial disorder so rare it is found in 1 in 65,000 to 88,000 babies. Now Stacy and John had entirely different questions: What would Justin’s quality of life be? Could he even go to school?
“When you have a child with special needs, your whole outlook is different because everything changes,” Stacy said, “so you have to find your new normal.”
The new normal included flights to the Craniofacial Center at Medical City Children's Hospital in Dallas for those surgeries, and what John said seemed like endless months in hotels, as well as nights where he and Stacy tried to sleep on the couch in Justin’s hospital room.
It also included Little League baseball and youth basketball, soccer and golf, and plenty of roughhousing with his cousins around the blueberry farm.
Stacy and John were determined to meet Apert syndrome head on.
Justin would do everything every other kid his age did. They signed him up for baseball when he was 4 even though he had trouble holding a bat because he doesn’t have knuckles in his fingers.
So what if he couldn’t hit the ball? Neither could the other 4-year-olds, John said.
It was the same way in school.
“Do not help him,” Stacy sternly told Justin’s teacher on her son’s first day of kindergarten. “He can do it.”
“I think I scared her,” Stacy said. “I just wanted to give him a chance. You have to give people a chance to be who they can be.”
Maybe people outside of school stared at Justin and made rude comments to Stacy, but at Foundation Academy, Justin was just one of the kids. His popularity grew as he moved up through the grades.
“There is something about Justin that makes everyone love him,” Foundation Principal Sarah Reynolds said. “He is so friendly, so kind. No one sees his disability. No one. It’s just a non-issue.”
With the education choice option that came with the McKay Scholarship, Stacy and John settled on Foundation Academy because they wanted a smaller scholastic setting for Justin, one where his teachers would know and understand his needs and where he could spend the years with the same classmates.
Having the scholarship pay his tuition was huge when Justin was undergoing his surgeries and treatments.
“We, honestly, would not have been able to keep him at the same school had we not had the scholarship,” Stacy said.
John put up a basketball hoop in the family’s driveway because he thought it was a game Justin could play. He was right. Justin was hooked at an early age.
Justin’s ability score on long-range jump shots earned him the nickname “J-Money” from his teammates because, as Hughes said, “He makes his money on the 3-point line.”
Justin was not the most talented player on the team, but Hughes said he made the most of his skills. He also understands the game, the way the offense and defense work. Hughes often asked Justin what he thought of something that occurred during a game, and Justin would offer an honest and accurate assessment.
He was also the teammate who kept everyone loose and focused.
“A glue guy you can’t live without as a team,” Hughes said.
As he walked out of the gym after every practice and game, Justin would always find Hughes and say, “Thanks, Coach. See you tomorrow.”
It was Hughes who nominated Justin for the Naismith award, and the school celebrated the announcement of Justin winning with a pep rally in front of the entire student body. They chanted his name and Justin took a shot, though opting for a high-percentage layup. The crowd went wild as the ball dropped through the net.
There were TV crews from Orlando-area news stations and one shooting a video for the award.
“I like sharing my story and having an impact,” Justin said.
“You need to lean on your family and friends because they are always there for you, no matter what you’re going through,” he said. “If you’re having a rough day or a hard time, always trust in God. He will make your path straight. I think people get down on themselves because they think they are not normal or not as good as someone else, but I think if they pray and follow God, they will be fine.”
College classes begin soon for Justin. He’s thinking of studying business. He will help Hughes coach this season and wants to someday coach high school basketball.
“He has totally superseded anything I envisioned for him,” Stacy said. “I never thought he would be as awesome as he is. He surprises you all the time. He has the best sense of humor. He never complains about anything. He’s always a try-hard kid, which blows me away.”
As for what she now envisions for Justin’s future, Stacy said, “I think it’s up to him. The sky is the limit. I can’t wait to see in five years where he’s at.”
Roger Mooney, manager, communications, can be reached at firstname.lastname@example.org.