Nemours Blog Posts | Expert Advice on Child Health & Wellness

Osteogenesis Imperfecta Awareness Week: Mackenzie’s Story

In the world of healthcare, finding a place that feels like home can be a challenge. For Amanda, mother of 4-year-old Mackenzie, that home is Nemours Children’s Hospital, Delaware. Mackenzie’s journey with osteogenesis imperfecta (OI) began even before she took her first breath. At just 25 weeks, Amanda learned of her daughter’s diagnosis. “I went for a routine anatomy scan while pregnant. Significant bowing in Mackenzie’s legs and long limb measurements indicated that she would need more testing. I received an amnio and was sent to another hospital where she was diagnosed,” Amanda recalls. Transitioning Mackenzie’s care to Nemours Children’s was a pivotal moment for their family. They discovered the facility after finding recommendations on social media. “We are part of a group on Facebook for parents of children with OI,” says Amanda. “I was asking questions when Mackenzie broke her arm at 10 days old and someone recommended we […]

Compassionate Care: Cruz’s Story

“At the 20-week ultrasound, I learned about his skeletal dysplasia,” Brittany recalls. “And at the 33-week Vistara blood test, I learned about his OI diagnosis.” These moments marked the beginning of Cruz’s journey, but they also sparked Brittany’s search for the best care possible for her son. It was during her 35th week of pregnancy that Brittany discovered the Advanced Delivery Program (ADP) at Nemours Children’s Hospital, Delaware, thanks to a recommendation on the Osteogenesis Imperfecta Community Facebook page. “Their care, communication, and knowledge gave us extreme confidence in the ADP Team,” says Brittany. “They had a plan, relayed it to us, listened to our concerns, and had experience delivering OI babies.” The support Brittany received from the medical staff at Nemours Children’s during the delivery process was nothing short of extraordinary. “They showed compassion during every step,” Brittany emphasizes. “They helped keep me calm by talking about my 2-year-old […]

From Pitch to Progress: Jarnum’s Story

In the world of sports, injuries are often seen as setbacks, hurdles that athletes must overcome to get back to doing what they love. For Jarnum, a 15-year-old elite soccer player, a left knee lateral meniscus tear threatened to impact his game. Jarnum is the youngest player in a semi-professional USL2 academy league for Swan City Soccer Club in Lakeland. He holds the distinction of being the youngest player ever to score a goal in the USL2, helping his team secure their sole victory of the season. Unfortunately, it was during his time with this team that Jarnum sustained his injury. While engaged in a defensive play, he collided with another player, resulting in the tear to his left knee. Jarnum’s mother, Authrine, recalls the moment when their journey with Nemours began. “Dr. Julia Fink could tell that it was a meniscus tear right away,” she says. “But she wanted […]

Axel’s Pectus Excavatum

From a young age, Axel’s family had noticed the unusual appearance of his chest. They took him to see a few different providers, but they were told that his chest was not responsible for his symptoms, and it was only a cosmetic defect. It wasn’t until Axel needed a checkup and couldn’t get into his regular pediatrician that his mom searched for another pediatrician. At that appointment, Axel asked his mom once again to mention his chest, and although hesitant due to their past experiences, she brought it up. This pediatrician immediately noticed that something was wrong and referred them to Dr. Kellianne Kleeman, a pediatric cardiothoracic surgeon at Nemours Children’s Hospital, Florida. Dr. Kleeman mapped out a detailed care plan that included a minimally invasive surgery to repair his pectus excavatum. Axel says, “When Dr. Kleeman showed us the picture in clinic—that was the first time I saw my […]

From Patient to Pre-Med: Maddie’s Story

At 13 years old, Maddie Walsh was diagnosed with melanoma. This unexpected turn led her to Nemours Children’s Hospital, Florida, where she found a supportive community that became like family. Maddie’s journey began with the discovery of a change in a mole she had since childhood. A dermatologist family member recognized the signs and urged her to seek medical attention. Following a biopsy and consultations with various pathologists, Maddie received the diagnosis of malignant melanoma from Chief of the Division of Plastic and Craniofacial Surgery, Dr. Brian Kellogg. “I was 13 when I first heard I was going to see a plastic surgeon. I was very confused because I only knew them by the stereotypes on TV,” says Maddie. “However, I quickly learned that was far from what Dr. Kellogg and his team does. When I first heard the word ‘cancer,’ my mind jumped to the worst. I was terrified. […]

Donate Life Month: Jamaica Pediatric Living Related Donor Liver Transplant Program

Growing up in rural Jamaica, Dr. Judith A. Jones was inspired by the idea of helping others. In a community where the only female healthcare professionals she saw were nurses, her older brother’s encouragement sparked the realization that she, too, could become a doctor. “It reinforces for me to this day how a casual comment can change the trajectory of a child’s life, making things possible that were not previously dreamt of,” says Dr. Jones. “My big brother told me I could be a doctor, and so I did, because it was the way in which I believed I could help people. As a young girl, I had an overwhelming sense that I should help people when I grew up. My parents were incredibly hard-working and were professionals despite coming from humble beginnings. Their example and encouragement also led me to pursue medicine as my life’s work.” Her career led […]

Limb Loss & Limb Differences Awareness Month: Jaiden’s Story

Jaiden’s medical journey began with a diagnosis of Fibular Hemimelia during a routine anatomy scan at just 20 weeks into his mother, Megan’s, pregnancy. Little did they know, this diagnosis would lead them to Nemours Children’s Hospital, Delaware. Upon learning about her son’s condition, Megan was very shocked. “It was unexpected, but we knew we had to do everything we could to give Jaiden the best chance at a fulfilling life,” she shares. “Though Jaiden always got around fine, if he didn’t have surgery, his legs would be drastically uneven and would not be able to walk.” Their journey with Nemours Children’s began in 2012 when Megan sought a second opinion on Jaiden’s condition. “A family friend suggested Nemours, and from the moment we walked through the doors, we knew we were in good hands,” Megan reflects. Dr. L. Reid Nichols, a renowned pediatric orthopedic surgeon, became an integral part […]

Donate Life Month: Luca’s Story

From the moment he was born, Luca has been full of surprises. He entered the world in February 2022, a month earlier than expected. Anticipating a baby girl, complete with a gender reveal celebration, Luca’s parents were surprised by his arrival. Their anatomy scan’s mistaken prediction left them pleasantly surprised by their baby boy. Shortly thereafter, concerns arose regarding Luca’s kidney health, along with some unfavorable lab results. Luca was transported to the NICU and later taken to Nemours Children’s Hospital, Delaware. “When the doctors at Inspira Mullica Hill started to get an inkling that Luca had serious kidney issues, they recommended right away that we be transferred to Nemours Children’s,” says his mother, Cory. “We appreciated their honesty so much, as they explained to us that they didn’t have the capability to deal with Luca appropriately. One doctor even said that if this was his child, he would have […]

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