Southern Maryland News

Pomfret family encourages people to see beyond facial difference­s

Pomfret family encourages people to see beyond facial difference­s

- By SARA NEWMAN snewman@somdnews.com Twitter: @indy_community

Anti-bullying messages are prevalent in today’s schools, but some kids still may not understand how mocking someone for their difference­s can have profound effects that last well beyond the school day.

“It breaks my heart,” Michelle Atfimos of Pomfret said of the bullying her son, Kyle, 8, has received at school.

Kyle Atfimos was born with a cleft lip and palate which left a visible gap on the right side of his upper lip. He recently had surgery to eliminate the gap — a bone graft process that took bone from his hip and added it to the gap in his mouth — which made the cleft lip less visible, but left Kyle with a slight limp and out of school for three weeks.

With help from individual­s from the Children’s Craniofaci­al Associatio­n (CCA), the Atfimos family has breathed a sigh of relief and helped Kyle realize he is not so different in the world as he often feels at school.

Cleft lip, with or without cleft palate, affects one in 700 babies annually, and is the fourth most common birth defect in the U.S., according to the associatio­n. Despite this, Michelle and Kyle said they knew virtually no one else that had it.

After a few instances when Kyle came home from school crying after bullying on the bus, Michelle said she and her husband, Nick, considered private school for him but realized they couldn’t afford it.

“That hurt me as a parent to see that and I can’t imagine how it is for him when he’s not there,” Michelle said.

“Especially because you can’t buy me a new face,” Kyle added.

During a yearly clinic visit when Kyle was 8 years old, Michelle said she realized how serious the bullying was affecting her son when a psychologi­st said Kyle should attend counseling. Michelle said she began to see how much this issue could grow for Kyle as he got older.

“I spoke with others and they said, ‘Kids will be kids,’” Michelle said in response to the bullying. “He’s kinda shy and he’s a kind kid and I’ve told him to stand up for himself, but he also doesn’t want to be a bully.”

Michelle set out to find support through the clinic and social networks with no luck until she contacted CCA. The organizati­on sent brochures and informatio­n on Kyle’s condition and its yearly retreat. It wasn’t until Michelle and Kyle read the book “Wonder,” by R. J. Palacio, now being made into a movie, that Kyle’s eyes opened to discover he was not the only one with this condition.

The book depicts the tale of a young boy, Auggie, born with a facial deformity and is about to begin fifth grade at a mainstream school. As the new kid, the book follows Auggie’s quest to show his classmates how he is just like them despite appearance­s.

“It made me feel like I wasn’t the only one and that some people have it even worse than I do,” Kyle said of the book. “It made me feel good and I’m sure it made other kids feel good, too.”

The family was also able to pull together resources to travel to Ft. Lauderdale, Fla., to attend the associatio­n’s annual Cher’s Family Retreat. Held in June, the event aims to provide individual­s affected by a facial difference, their siblings and parents an opportunit­y to interact with others who have endured similar experience­s. Again, Kyle found himself among children and families just like his, including a local family from Bel Alton.

“The retreat was so heartwarmi­ng because these kids would just come up to us and hug us, like they knew we were safe to come up to. We weren’t going to be afraid of their facial difference,” Michelle said.

“My favorite part of the retreat was when I made new friends and found a friend that lives nearby,” Kyle said.

Now that Kyle has had his surgery, Michelle hopes the bullying will subside and the confidence Kyle built up over that summer will not diminish during the school year. She aims to encourage local schools to add the book, “Wonder,” to their curriculum — she says it encourages kids to “choose kind” — and take advantage of a field trip grant for Kyle and his classmates to attend the movie premier of “Wonder,” in theaters April 7, 2017.

Above all, she said she wants her son to be happy.

“I just want to know that he’s OK and is happy and isn’t worried about going back to school,” Michelle said.

 ??  ?? Kyle Atfimos, 8, smiles with “Wonder,” a book that is now being made into a movie. The book helped him realize his difference­s — being born with a cleft lip and palate — did not warrant bullying. His mother, Michelle, hopes local schools will...
Kyle Atfimos, 8, smiles with “Wonder,” a book that is now being made into a movie. The book helped him realize his difference­s — being born with a cleft lip and palate — did not warrant bullying. His mother, Michelle, hopes local schools will...
 ?? STAFF PHOTOS BY SARA NEWMAN ?? Kyle Atfimos and his mother, Michelle, smile with various gifts they’ve received from friends and strangers after attending the Children’s Craniofaci­al Associatio­n annual retreat. Kyle was born with a cleft lip and palate that has made him the subject...
STAFF PHOTOS BY SARA NEWMAN Kyle Atfimos and his mother, Michelle, smile with various gifts they’ve received from friends and strangers after attending the Children’s Craniofaci­al Associatio­n annual retreat. Kyle was born with a cleft lip and palate that has made him the subject...

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