Some people spend years trying to find their mission in life. For sweet Piper Grace Hoefler, it took just 27 days. Piper passed away from the effects of Spinal Muscular Atrophy (SMA) Type 0, but her legacy lives on in books about inclusion donated by her family’s charitable organization, Piper’s Key. “I didn’t want to […]
As with mostly everything else, siblings embark on their weight loss journey – together
It would be difficult to find a brother and sister closer than Lorenzo and Zaryiah Haynes. Just 19 months apart in age, they have always been each other’s best friend. They attend the same Akron high school and share the same interests in entertainment and sports. They laugh at the same jokes and like the […]
Healthy Roster App helps athletic trainers manage athletes’ injuries
As a mom of a multi-sport athlete, Amy Hitchcock is no stranger to sports injuries. But what she wasn’t used to was a streamlined approach to communicating her child’s injury and plan of care between herself and his provider, coach, school and athletic trainer – that is, until recently. Hudson Middle School, where her 13-year-old […]
Care at Akron Children’s Special Care Nursery helps Lorain family through difficult time
When Stacey Dickson started feeling unwell, she didn’t think it would result in the early birth of her son. What began as a nagging pain in her back between her shoulder blades progressed into life threatening high blood pressure. After consulting with her obstetrician, Stacey went to Mercy Health – Lorain’s labor and delivery triage […]
Evan Wooldredge cooks up his next stage of life after beating rare genetic disease
Evan Wooldredge, age 18, is the kind of person who is always up for a challenge. Whether he’s creating a new menu item at work, learning to golf or managing a rare disease that affected his kidneys, Evan doesn’t let restrictions hold him back. One of Evan’s biggest challenges happened when he turned 10. After […]
Medical genetics journey leads East Liverpool family to a surprise and a diagnosis for their son
It took Heather McCune and her fiancé, John Scott, three years to get a diagnosis for their son and learned something quite remarkable. He is the third-known child to be diagnosed in the world with a genetic condition so new it does not have an official name. Heather, who lives in East Liverpool, recognized almost […]