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Friday, August 11, 2017
At Signature Flight Support at Logan Airport, April Lanord waited for a visitor to arrive. Her son, Alec Bruneau, 14, stood by with mixed emotions – excitement, curiosity and just a touch of nerves. Up to this point, they had never met another person with Myhre syndrome – an extremely rare genetic condition that Alec was diagnosed with less than a year before. They were anxious to share pizza in the North End before their visitor’s appointment at the Myhre Syndrome Clinic at MassGeneral Hospital for Children (MGHfC) and Massachusetts General Hospital.
Since opening in January 2017, Lanord, of Plymouth, Mass., has been an unofficial ambassador for the clinic, helping to get patients and families oriented to the hospital and to the city. Before families arrive, she gives them suggestions on where to go, what to do and where to stay. “Families don’t have a whole lot of time here in Boston because they’re here for an appointment, not for a vacation,” said Lanord. “I’ll help them find things to do that are local and fun because I know how scary it can be to be far away from home and to be dealing with a rare condition that has a lot of unknowns.”
Myhre syndrome causes a wide variety of symptoms that range in severity, including a distinctive facial appearance and posture, short stature, learning challenges and heart problems. Since the first reported case in 1981 and the initial 60 cases reported in the literature, there at least 50-100 people estimated to have Myhre syndrome in the United States.
At around 18 months old, Bruneau began to show signs of significant medical issues. He had chronic ear infections and was consistently falling off the growth chart at his pediatrician’s office. As he grew up, Bruneau had seven sets of ear tubes, bi-lateral hearing aids, a tumor in his shoulder and distinctive facial features. An earlier diagnosis of mild aortic stenosis also led doctors to believe he was a medical mystery.
After being diagnosed at another Boston hospital, Lanord brought her son to MGHfC to see Angela Lin, MD, co-director of the Myhre Syndrome Clinic and a medical geneticist who is already familiar with the condition. The multispecialty clinic includes a core of providers from Medical Genetics, Pediatric Cardiology, Cardiovascular Imaging, the Airway, Voice and Swallowing Center, Pediatric Pulmonary Medicine and Pediatric Rheumatology. She had learned about Lin on a social media group for families whose children have Myhre syndrome.
“The key to caring for any patient with a rare disorder is creating a partnership between the patient, their family, primary care provider and the specialists. It helps to have one person as the coach or coordinator, which is how I try to help,” said Lin. “We work with each family to create a plan that works for them based on the family and patient’s unique needs. I call it their MGHfC and Mass General genetic medical home, although their primary care is always ‘home base.’ MGHfC is ideal for that because we have more than 50 medical and surgical specialties and we provide care across a person’s lifespan, giving attention to the transition years.”
Coming to the Myhre Syndrome Clinic was life-changing for both Bruneau and Lanord. The care he received helped Bruneau cope with and understand his diagnosis, leading him to flourish socially, emotionally and physically. In addition to receiving care from Medical Genetics, Bruneau also sees providers from Pediatric Cardiology, the Airway, Voice and Swallowing Center, Pediatric Pulmonary Medicine and Pediatric Surgery.
“Before our first appointment with Dr. Lin, I told Alec that we were going to a clinic for special children just like him, which was amazing to hear because both he and I had never met anyone else with Myhre syndrome,” said Lanord. “After that, it was like he found a sense of comfort knowing that he isn’t alone and that there is an answer to his medical issues. He became more confident knowing that there is a place for him and children like him.”
Having people like Lanord plays an important role in the care that the Myhre Syndrome Clinic provides. “A specialty clinic could not begin to do its work without the energy and support of caregivers like April,” said Lin. “I think of her as our ‘Massachusetts Ambassador!’”
It’s that sense of community and belonging that drives Lanord to continue to meet with patients and families in the Myhre Syndrome Clinic. “When we were at dinner with our visitor, they looked at me and said ‘You get it. You understand what it’s like to live with this condition,’” said Lanord. “I’m a mom and I know what Myhre syndrome is. I know how lonely and scary it can be. Knowing someone who’s been through a similar situation makes it just a little easier.”
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