Stories about: Dr. Peter Waters

Jenna’s story: How two surgeons changed her path in life

Inspired by her own surgeries, Jenna dresses up as doctor

“Your daughter was a very sick little girl.” Those were the first words that came out of Dr. Peter Waters’ mouth as he addressed my parents in the waiting room of Boston Children’s Hospital, back in 1999. They had been anxiously waiting, wondering and worrying about my condition.

“Will they get it all?”

“Will she be the same?”

“Will she survive?”

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Breaking down the facts about fractures

Learn all about fractures in children.

Thousands of children, adolescents and young adults come through the doors of Boston Children’s Hospital’s Orthopedic Center every year with the same diagnosis – fracture. Whether on the wrist or the ankle or anywhere in between, a fracture can be painful and restricting to an active child or teen.

What is a fracture?

A fracture is a bone that is partially or completely broken. There are two types of fractures:

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Grabbing the reins her own way

Chloe, a roder rider with brachial plexus, rides a horse during a barrel race.
Chloe Neff, a rodeo rider with brachial plexus birth palsy, will compete in barrel racing world championships. 

Barrel racing isn’t for the faint-hearted, that’s for sure.

In this rodeo event, horses and riders whip around barrels at lightning speeds. Tails flourish in the air and muscles ripple. Powerful horses are coaxed by their riders to spin around each barrel as quickly as possible.

One such duo, 16-year-old Chloe Neff and her horse, Raise a Glass Dancer, will soon be on their way to barrel racing’s world championships.

“If you keep trying and working at it, you can do anything you want to,” says Chloe. Her record for completing a barrel course is 16.6 seconds. “Right now, Glass and I are working toward a 15.”

In the Perry, Georgia, stadium where barrel racing world championships will be held later this year, Chloe’s parents may be the only people to notice anything seemingly different about Chloe, as she and Glass flash past the stands. That’s because Chloe, who has received care from the Brachial Plexus Program at Boston Children’s Hospital since she was 5 months old, sustained damage to her left brachial plexus nerve when she was born. The injury jeopardized Chloe’s use of her left shoulder, elbow, wrist and hand.

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Celebrating Aiden and Aiden: Making a difference for kids with limb differences

radial ray deficiencyFour-year-old Aiden Quinn is looking forward to his birthday celebration on Nov. 22. There will be plenty of cake, treats and friends. One friend sure to be right by his side is Aiden’s sidekick, namesake, best friend and travelling companion — his Aiden doll.

Aiden the boy was born with a radial longitudinal deficiency of his forearm and hand. He had no radial bone — one of the forearm bones in his left arm. The ulna — his other forearm bone — didn’t grow properly either, and his left thumb had no muscles or bones.

Aiden the doll is a hand-crocheted toy that sprung to life on April 18. The boy and doll share a name and a mission: raising awareness about limb differences.

“I wanted to find a way to connect kids with limb differences,” explains Aiden’s mother Jennifer.

Aiden the baby

Though Aiden the doll is just a few months old, the idea of connecting families of children with limb differences stretches back several years to when Jennifer was pregnant with Aiden.limb difference

A prenatal ultrasound showed the deformity in Aiden’s left arm. “I was scared and helpless and alone, and I needed answers,” recalls Jennifer.

The Long Island, New York mom started looking for specialty care for her unborn son. “The deformity is rare enough that doctors didn’t know about it, or they were intimidated by babies,” she says.

Then she and her husband Dan found Dr. Peter Waters, Orthopedic-Surgeon-in-Chief and director of the Hand and Upper Extremity Program, and met with him prior to Aiden’s birth.

“It gave us peace of mind. He answered our questions, and we felt more secure,” Jennifer says.

Aiden the boy

radial ray deficiency
Aiden showing off his banana-peeling skills

In the last five years, Aiden has undergone six surgeries with Waters. The surgical goal for kids with radial ray deficiencies, says Waters, is to improve both function and appearance.

Those surgeries have not only repaired Aiden’s left arm and hand, they also have strengthened his character and inspired Jennifer to raise awareness about limb differences and provide support for families like hers. She created the Aiden doll to help her achieve that goal.

“Our son Aiden is happy, creative and goofy. He wears his heart on his sleeve and loves to sing and dance. He might be a bit headstrong, but that determination gets him through,” says Jennifer.

Jennifer hopes that Aiden the doll can help infuse a similar spirit of determination, strength and pride in other children with limb differences.

“I’m astonished by how Aiden manages to do things,” Jennifer continues. Aiden has found a way to peel a banana using his pinky and can even out-peel his 3-year-old brother.

Aiden the escape artist

Jennifer may not be the only one astonished by her son.

“Dr. Waters calls him his most trying patient,” jokes Jennifer.

Aiden managed to wriggle out of two casts placed after wrist centralization (correcting the significant deviation of the wrist) and thumb pollicization (making a thumb out of his index finger).

limb difference
Dr. Waters with Aiden the doll and Aiden the boy

“One or two out of every 500 kids can figure out how to get out of a cast. Aiden is one of those kids,” says Waters. “It can be quite a burden for families like the Quinns, who aren’t close to Boston.”

Waters works a local orthopedic surgeon closer to the Quinn’s home in Long Island. The local physician manages some aspects of Aiden’s care, which helps the family minimize the number of trips to Boston for Aiden’s treatment.

Aiden the doll

As the Quinn family brainstormed ways to raise awareness about limb differences, Jennifer reached out to Tani Correia, a crochet artist who designed and donated two dolls to Limbtastic, the limb-differences awareness, support and advocacy organization Jennifer founded.

Tani mailed the dolls to the Quinn family, and Aiden promptly named the dolls after himself.

One doll hangs out with Aiden. They go to the playground and preschool together, and the doll even traveled with Aiden and his parents to his most recent appointment with Waters.

The other Aiden doll is a jet setter and travels across the U.S., visiting children with limb differences, spending a week with each family, who then record the visit in a notebook that travels with the doll.

“It’s amazing to see how many lives the doll has touched,” says Jennifer. In the summer of 2015, Aiden the doll traveled to Camp Joy, which is sponsored by Amputee Coalition, and met 115 campers and 33 counselors with a limb loss or limb difference.

“These kind of organizations and networks, with families supporting each other and working together to raise awareness, can really help children reach their potential and families realize they aren’t alone,” says Waters.

Learn more about the Boston Children’s Hand and Orthopedic Upper Extremity Program.

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