A family’s journey with developmental dysplasia of the hip (DDH) typically starts when a baby’s pediatrician hears a click in her hips. The next steps often include an ultrasound and a follow-up with an orthopedic surgeon, perhaps a pediatric hip specialist.
College friends Tosha LoSurdo and Jessica Rohrick recently re-connected after their babies were both diagnosed with and treated for DDH at the Boston Children’s Hospital Child and Young Adult Hip Preservation Program.
Tosha’s daughter, Carmela, and Jessica’s daughter, Phallon, were treated with a Pavlik harness and are on a regular follow-up schedule with their pediatric orthopedic surgeons — Drs. Eduardo Novais and Travis Matheney.
The new parents offer advice for other parents whose babies are diagnosed with DDH. …
A few months ago, Hunter VanBrocklin was barely managing a 1 mile-per-hour pace on the treadmill. That was before his surgery to treat hip dysplasia.
“I went past 1 mph already. Say good-bye,” brags Hunter, who’s not only managing a brisk 3 miles-per-hour pace, but also recently returned from a trip to Washington D.C. for Family Advocacy Day. The annual event brings families from children’s hospitals across the U.S. to the capital to meet with their senators and representatives to share their medical stories and encourage lawmakers to improve access to high-quality pediatric care.
This year, Boston Children’s staff and families sought to secure sponsorship for the Advancing Care for Exceptional (ACE) Kids Act of 2015, a bill that makes it easier for children with medically complex conditions who rely on Medicaid to get the care they need at children’s hospitals, especially when they have to cross state lines. …
For the women’s crew team at College of the Holy Cross and rowers everywhere, all eyes are on the Head of the Charles Regatta. It’s a long journey for every rower participating in the sport’s ultimate competition. But few have come so far as Caroline Laurendeau, the 4’11” coxswain for the Holy Cross Crusaders women’s rowing team.
Caroline, who was born weighing just 1 lb. 11 oz., spent the first four-and-a-half months of her life in Neonatal Intensive Care Units (NICUs) at Boston Children’s Hospital and Beth Israel Deaconess Medical Center.
Those first few months were hectic and scary for Caroline’s family. At one point, she suffered a pericardial effusion — fluid had accumulated around her heart. “The mortality rate from that can be really high,” explains Dr. Jane Stewart, director of the Boston Children’s Infant Follow-up Program. Physicians at Boston Children’s tapped the effusion to release the fluid and save her life.
Boston Children’s Hospital strives to create a comfortable, supportive environment for all of its patients. Still, most can’t wait to leave the sterile hospital halls and return to the comfort of their own homes. Anna, a 20-year-old college student from N.H., has other thoughts.
“I can’t wait to come back to Boston Children’s.”