Anyone taking their eyes off the Target Center court one day last winter might have spotted two basketball junkies in the expensive seats, talking with their hands, rating players, comparing ambitions and ailments.
The man wore the mien and wardrobe of an executive. The boy wearing the Timberwolves jersey could have been his son, but this wasn't just another night of male bonding.
The man was Timberwolves assistant general manager Fred Hoiberg, who was forced to retire from the NBA because of a heart condition. The boy was Matthew Gamber, 12, a sixth-grader from Brooklyn Park who has clung to life since being born with a variety of life-threatening illnesses, including a growth around his heart. A network of mutual friends brought them together, leading to a few of the best days of Gamber's life. For all of the corruption in big-time athletics, you don't have to look far to find someone as giving as Hoiberg, or as buoyed by sports as Gamber. The night he spent next to Hoiberg in the stands gave them a chance to talk about the intricacies of basketball and the fragility of life.
"But all Matthew wants to talk about is basketball," Hoiberg said. "I think when anybody has something involving their heart, you do create a bond with that person. What he's gone through is a lot tougher than what I had to go through.
"He's had 100 surgeries already. I had one, at 32 years of age. He's just a kid. If we can bring him to a game like this and put a smile on his face, that's the important thing."
Gamber's family and support system at Monroe Elementary in Brooklyn Park, where this story started, would agree.
"There are really two heroes here," said Gregg Scherer, a teacher at Monroe and usher at Wolves games who helped bring everyone together. "Fred is someone for Matthew to look up to, but Matthew is someone Fred can look up to, too.
"This is a miracle child."
A fragile beginning
When Gamber was born, doctors questioned whether he'd ever be able to sit up, speak or walk, much less become an aspiring athlete and devoted sports fan.
When he was 3 days old, Matthew stopped breathing. Pediatricians at Fairview-University Medical Center saved him and diagnosed his condition as a rare inborn metabolic disorder known as ornithine transcarbamylase deficiency.