Twin brothers Luke and Brett Hanson are an unmistakable one-two punch for one of the basketball team from Special Opportunities Available in Recreation, or SOAR, the team that participates in numerous Special Olympics competitions, and is jointly funded by the Parks and Recreation Departments of the Town of Normal and City of Bloomington.
The 14-year-old twins are students at Evans Junior High School and are part of the SOAR Supermen team, coached by Miranda Henson and Spencer Reed. The guys and their teammates had their hands full when they participated in the Ron Knisley Memorial Shootout at Shirk Center at Illinois Wesleyan University on Dec. 31.
The Ron Knisley Memorial Shootout is a two-day event woven into the annual State Farm Bloomington-Normal “Classic†Holiday Tournament. When he died after battling cancer in the fall of 2005, Knisley served as Director of Sports and Competition at Special Olympics Illinois, headquartered in Normal. He also was a 10-year member of the committee that helped put together the Bloomington-Normal State Farm Holiday Tournament. As the planning for the “Classic†grew, Knisley gave his fellow committee members something to consider: A tournament within the tournament, consisting of Special Olympics basketball teams. It was embraced whole-heartily Knisley’s fellow committee members.
The Hanson brothers have been active in Special Olympics for seven years, including being part of SOAR’s basketball program, explained their parents, Greg and Lori Hanson, Bloomington, where the boys attend George L. Evans Junior High School.
With individual personal trademarks clearly visible to the crowd that came to see teams compete – Luke’s red socks and Brett’s blue bandana – the brothers clearly want opponents to know they will have a battle on their hands on the court. And even off the court, the 14-year-olds have come a long way, their parents say.
The eighth grade duo don’t just participate in Special Olympics, but were also part of EJHS’ Cross Country team, running two miles. “Our teacher lets us leave school early so we can go to meets,†Luke said. The boys even get a little running time in as members of EJHS’ “Run Club†in the summer, he added.
They both enjoy basketball and trying to keep their team in a game. But, with an average height of 5 feet, against the Pink Panthers from Pekin Park District-managed Illinois River Valley Special Recreation Association, a team with players averaging 6 foot or taller, the Hanson brothers and their teammates had their hands full, losing the opening game of the day, 38-12, in a valiant effort.
Greg and Lori Hanson wanted their sons to make more than a valiant effort as far as their lives are concerned, especially after they turned 6 and each of the boys had been diagnosed by doctors with Cardiofaciocutaneous Syndrome, or CFC, a rare genetic condition that typically affects the heart, facial features, and skin. It affects 1 in every 810,000 births, Lori Hanson told me.
Born prematurely and not meeting all the little milestones of growing children, doctors weren’t real positive when giving an outlook to the Hansons for the boys, Lori Hanson explained. Despite that, Greg Hanson said, “We didn’t treat the boys like a syndrome.â€
“They’ve always had high energy, and Special Olympics and basketball is a good outlet for that energy,†Lori Hanson explained.
“We play a lot of basketball together,†Greg Hanson added. “We work on shooting and passing.â€
When they aren’t playing basketball or active in Track and Field at EJHS, the boys bike, something Brett said he enjoys. In fact, they’ve been known to do 25 miles going north to south along Constitution Trail. But they have to bike five miles from their home to reach an artery of the Trail to do that, Greg Hanson said. So, they get a workout in to be sure.
In fact, all the biking the boys get in gave Greg Hanson an idea. He would like to have his family enter this year’s Ragbrai event in Iowa in July. Ragbrai, or Register’s Annual Great Bicycle Ride Across Iowa, is a non-competitive bicycle ride organized by The Des Moines Register, going across our neighboring state from west to east. Along that proposed journey, Hanson said, he would like to try to educate folks about CFC.
The Hansons’ hopes for their boys’ futures are to see them take courses in high school and move on to college. Doing that will make Luke and Brett able to join the rest of the world’s productive adults when that time comes, their parents believe.
Lori Hanson said, “We want to see our boys treated as anyone else would be.†She said she and her husband don’t want the boys to grow up feeling they need special treatment due to their medical circumstances.
That means the Hansons want their sons to be granted a chance to be treated like everybody else in this life. That all any parent with a child with a disability wants. And from what I learned from the Hansons, it’s a chance guys like Brett and Luke, and girls, too, all deserve.