childrens hospital Archives - Nemours Blog

ARTICLES RELATED TO:
childrens hospital

Doctors’ Day Spotlight: R. Lawrence Moss, MD, FACS, FAAP

Nemours Children’s takes pride in spotlighting the remarkable individuals who go beyond their roles as physicians. R. Lawrence Moss, MD, FACS, FAAP, is president and CEO of Nemours. In addition to leading Nemours and advocating to redefine children’s health, Dr. Moss is an avid outdoorsman who loves the personal challenge of extreme sports. A pediatric surgeon of more than 25 years, Dr. Moss joined Nemours in 2018. On his office wall is a large frame full of thank you cards from families. Photos of four infants at the top of this catch his eye. “Those four babies are kids that I put on ECMO in the very early days of ECMO,” says Dr. Moss. “In each case, the family was told by the referring hospital that their newborn was going to die unless we tried a last-ditch, Hail Mary therapy called ECMO. All of those babies lived. They have all […]

Child Life Month: Laurel’s Associate Highlight

Laurel’s path to a career in Child Life began during her childhood. At just 3 years old, she experienced the passing of her younger brother due to SIDS, setting the foundation for her comprehension of grief. “I think that experience planted an empathy seed within me,” says Laurel. “It’s really special how I am able to use my experiences to support families here at Nemours Children’s. I’m able to understand grief within a family dynamic, including the sibling perspective, and share my insights, along with my training, into its effects on daily life and a family’s ability to cope.” In fifth grade, Laurel encountered child life firsthand during a hospitalization for a urethral reimplantation. From preparation for surgery to post-operative support, she found peace in the playroom activities and therapeutic interventions facilitated by her Certified Child Life Specialists. It was during these years that she discovered the importance of psychosocial […]

Dillan’s Hearing Loss Journey

Dillan’s hearing loss was discovered during a routine hearing scan, revealing that she was deaf in her left ear. While Dillan’s family had noticed some challenges with communicating before seeking treatment at Nemours Children’s Hospital, Florida, they were shocked to learn this news. Her family was very eager to find answers and solutions. Having been involved with the groundbreaking of Nemours Children’s Hospital, Florida 10 years ago, Dillan’s family was drawn to the comprehensive care provided under one roof. “Nemours provided seamless care. I love being able to communicate with her doctors in real time,” says Dillan’s mom. With the help of Dr. Morgan Wilcox, Dillan now has a hearing aid for her left ear, making an incredible difference in her hearing. “From the first day I met her, Dillan is always smiling and just has this contagious, feel-good attitude that you can’t help but smile and laugh along with […]

Jade’s Scoliosis Story

Jade has always been passionate about dance and yoga. One of her favorite hobbies is practicing yoga with her aunt. When Jade was 11 years old, her aunt noticed that her left rib was bulging out during one of their yoga stretches. This realization, along with Jade’s complaints of back and rib pain, raised concerns for her parents, especially since her mother was diagnosed with severe scoliosis at a young age. Based on her experience, Jade’s mom knew she had to act quickly so she immediately scheduled an appointment with their pediatrician to get a back check. At age 11, Jade was diagnosed with scoliosis and recommended to Nemours Children’s Health, Jacksonville. Jade and her family met with Anna Rambo, MD, an orthopedic surgeon at Nemours Children’s Health, Jacksonville. After their first appointment, they knew they made the right decision in choosing Nemours. They immediately loved everything about Dr. Rambo. […]

Lulu’s Cancer Story

In May 2021, the Italiano family was faced with news that would forever alter their lives. Luciana Italiano, affectionately known as “Lulu,” was diagnosed with Stage L2 Neuroblastoma at just three days old. Luciana’s diagnosis came unexpectedly when a tumor was discovered on her neck shortly after birth. “May 19 was a great and exciting day that turned into nightmare,” says, Lulu’s mother, Carey. “It is an intimidating experience when a newborn baby receives a cancer diagnosis,” says Nemours Children’s Health Hematologist/Oncologist, Dr. Andrew Walter. “Instead of simply celebrating the joy of welcoming a new, healthy child into the world, family members must quickly meet with pediatric specialists and consultants to discuss diagnosis and treatment options and undergo a series of test and procedures. The family doesn’t even have the time to go home and rest.” After being transported to Nemours Children’s Hospital, Delaware shortly after Lulu’s birth, the hospital became the […]

A Calling for Care: Timothy’s Associate Highlight

Critical Care Flight Nurse Timothy McCormick grew up in a family of medical professionals. In fact, his mother is a critical care nurse. His parents instilled in him the values of faith, community, education, and helping others. “I decided early on in my education to pursue a career in nursing and gravitated to critical care medicine,” says Timothy. “Its challenging environment and unique clinical cases provide the immense reward of aiding in the recovery of critically ill patients. I consider my profession as a registered nurse a calling.” Timothy began his nursing career in the Adult Critical Care setting. During this time, he worked both inpatient and in interfacility EMS as a Critical Care Transport RN. He cared for critically ill adults, obstetric patients, and pediatrics for the first 11 years of his career. Eventually, Timothy made his way to Nemours Children’s Hospital, Florida while seeking an opportunity to expand […]

Overcoming Hip Dysplasia: Julieth’s Journey

Discover the inspiring story of Julieth, who was diagnosed with hip dysplasia at a young age. Learn about her treatment at Nemours Children’s Health and the impact it had on her life.

Cerebral Palsy Awareness Month: Logan’s Story

During the first trimester of her pregnancy, Christine Miller learned her son, Logan, was diagnosed with congenital cytomegalovirus infection (CCMV). Christine was told that her son was dying in utero and would likely not survive the birth. Since the CCMV diagnosis, the Miller family has been in constant contact with the infectious disease department at Nemours Children’s Health. At 32 weeks pregnant, Christine underwent an emergency C-section and Logan was born, weighing just 3 pounds. Immediately following birth, multiple calcifications were discovered on Logan’s brain. At this time, Logan was also diagnosed with Cerebral Palsy. Fast forward 18 years, Logan and the Miller family still have a very close relationship with Nemours. In 2021, Logan had his first appointment with Dr. Shrader (Dr. Dabney followed Logan since birth). At first, Dr. Shrader was very pleased with Logan’s movement and progress from his previous hip surgeries. “But after talking with him […]

Page 1 of 1

Page 1 of 1

Page 1 of 1