Published on in Community Impact Report
Every summer since 2010, Catherine Hamilton, BSN, RN, an inpatient nurse on the 7 West unit at Children’s Hospital of Philadelphia, packs her bug spray and sunblock and heads to Dragonfly Forest, an overnight summer camp for kids with special medical needs.
“I love it,” she says, “because we get to see kids outdoors, being healthy, doing everything any other kid would do at an overnight camp. I appreciate the children as children — not as patients. I’m in awe of them.”
Hematology week is one of five camp weeks at Dragonfly Forest. Other sessions are set aside for kids with persistent asthma, autism and 22q deletion syndrome. And one week is designed to help teens transition to adulthood. For the three summers since the Greater Philadelphia YMCA assumed leadership of the program, camp has been held at YMCA Camp Speers in the Poconos.
Every day of each week, a minimum of one physician and three nurses — plus respiratory therapists for the asthma week — are needed to staff the “Getaway,” aka the infirmary. “But we aren’t stuck in there,” Hamilton says. “We go with the kids for their activities, participate in the talent show, immerse ourselves in the fun.”
She has fond memories of taking a young boy with sickle cell on his first canoe ride across the lake and watching a teen with hemophilia disease zip lining. “These are things they’ve never done before, but with extra precautions, we made it happen,” she says. “It’s wonderful to experience it with them.”
Instead of being the “different” kid, at Dragonfly Forest, the kids are just like everyone else. “Everyone understands what they go through,” Hamilton says. “For once, they’re in the majority.”
“I get such joy seeing the kids doing some of the things that they might not ever have the chance to,” says Jennifer Hill RN, BSN, CPN, a nurse in the Apheresis Center who’s volunteered for nine years at Dragonfly Forest and for 12 years at a similar camp before that. “I also enjoy seeing them when they are well rather than only seeing them when they are sick. They can be completely different children when they are not in the hospital.”
Caylin Bolden, now 13 and a six-time camper, looks forward to camp every summer so she can reconnect with other kids with sickle cell disease she's become friends with over the years.
“I’ve met so many people at camp, and it’s really great to see my friends each year,” she says. “There, people understand you. It’s not like at my school, where not many kids know about sickle cell disease.”
It was hard for Caylin to pick her favorite part of Dragonfly Forest, “because everything is so much fun. If I have to pick, I’d say the lake and beach. There are canoes and hammocks. It’s really pretty there.”
Knowing that CHOP staff are on hand, taking care of medical needs as they arise, “gives parents peace of mind,” Hamilton says.
That was certainly the case for Melissa Bolden, Caylin’s mom. “The first year I was nervous,” Melissa says, “but I trusted other parents who told me, ‘Send her. She’ll be fine, and you’ll be happy.’ She hasn’t missed a year since. She loves it so much we had to change our vacation week so she could still go to camp.”
“There’s something magical about being there,” Hamilton says.
Categories: In the Community