Guest Contributor, Author at Nemours Blog - Page 19 of 28

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Meet Dr. Corrine Bria and Dr. Peace Madueme

Say hello to Dr. Corrine Bria and Dr. Peace Madueme! This dynamic duo from Nemours Children’s Hospital, Florida, is another one of the amazing couples on our team. Dr. Bria attended medical school at the Lewis Katz School of Medicine at Temple University in Philadelphia, Pennsylvania, and Dr. Madueme attended medical school at the Eastern Virginia Medical School in Norfolk, Virginia. The couple met during their pediatric residency at Cincinnati Children’s Hospital in 2017. Immediately following their residency, Dr. Bria and Dr. Madueme made the big move to Nemours Children’s Hospital, Florida. Today, Dr. Bria works in the Pediatric Emergency Medicine and Graduate Medical Education departments and Dr. Madueme in the Pediatric Heart Institute. Dr. Bria also served as one of the inaugural associate program directors of the pediatric residency program and is now the interim program director.  Dr. Madueme serves as the medical director of cardiac imaging and provides […]

Meet Dr. Gary Josephson and Dr. Patricia Solo-Josephson

In the world of medicine, it’s not uncommon for doctors to meet for the first time while in school, during their residencies, or even at a hospital! That’s how Dr. Gary Josephson and Dr. Patricia Solo-Josephson first met—in Miami, Florida at Jackson Memorial Hospital. Later, in the year 2000, Gary was offered an ENT position at Nemours Children’s Health, Jacksonville. The pair decided to make the move to Jacksonville from Miami and the rest is history! In 2016, Patricia also joined the Nemours Children’s team when she was offered to work as a pediatrician in the telemedicine division in Jacksonville. Today, Gary is the Chief Medical Officer of Nemours Children’s Health, Jacksonville and Patricia works in the Telemedicine Division of the Center for Health Delivery Innovation. Dr. Josephson and Dr. Solo-Josephson love the vision and mission of Nemours. They both cherish the opportunity to work for an organization who cares […]

Meet Dr. Maria Petrini and Dr. Francisco Vranic

Let us introduce Dr. Maria Petrini and Dr. Francisco Vranic, one of our many pairs of married doctors that work for Nemours Children’s Health! Dr. Petrini and Dr. Vranic met during their first pediatric residency program at a children’s hospital in Buenos Aires, Argentina. Dr. Vranic was a senior resident and Dr. Petrini was an intern. They bonded over their shared passion for pediatric medicine and the joy they found in caring for children. Upon their decision to move to the United States, Dr. Petrini was accepted to train in pediatrics at the Nemours Children’s/Thomas Jefferson University program and she stayed working at Nemours after graduation. A few years later, Dr. Vranic started his second training in pediatrics at the same program and took a position at the Saint Francis Primary Care office after graduation. Today, Dr. Petrini works as a primary care pediatrician at the Rockland Road Primary Care Office (Green Module) […]

Nothing If Not Resilient – Kate’s Story

During her senior season of high school wresting, Kate felt something was off. When Kate’s right shoulder dislocated from her socket during a wrestling practice, pain started to occur. Kate dismissed it at first but soon, this pain became persistent during every practice and started to impact her everyday life.  Her shoulder constantly dislocated while out on the mat and it held her back from taking good shots against opponents. Kate continued to persist through the pain until she could no longer reach for something or close a car door without discomfort. “When I walked through the halls at school, I felt my shoulder being separated from the socket. It felt loose – that’s the only way I can describe it. It is a scary feeling when you know that your arm is not properly attached to your body, let alone wrestling with it,” says Kate. This injury had a […]

A Few Months of Hard, For a Lifetime of Walking

At 18 months old, my physical therapist noticed I was showing early signs of a condition that needed attention as soon as possible. When my physical therapist suggested my family schedule an appointment with an orthopedic team, my family came to Nemours Children’s Hospital, Delaware; I was diagnosed with diplegic cerebral palsy. I’m now 12 years old and love my care team at Nemours. Dr. Peter Gabos and Dr. Jason Howard mapped out a plan for muscle lengthening and surgical femur/tibia reconstruction. The road to recovery was both a mental and physical battle that I will never forget. Some days it’s a challenge getting around with leg braces and very tiring, but I’m determined. All the doctors and physical therapists are so nice and helpful. They push you to do more than you thought you could, and I wouldn’t be where I am today without them. I’m hoping that I […]

Just Keep Dancing — Summer’s Story

Tammy noticed her daughter’s size difference from a young age. Summer was consistently smaller than her peers growing up, but her parents and pediatrician never suspected a serious issue. When Summer was about 7 years old, the family took a trip to Disney. Unlike their previous vacations, Tammy and Erik realized that Summer was struggling to keep up. This behavior was concerning because it was not the norm for their bubbly, energetic daughter. Unfortunately, Summer’s limp worsened, she experienced immense stiffness and hip pain, and she struggled to do what she loves most: dance. After an attempt at physical therapy, many x-rays and testing, Summer was diagnosed with Multiple Epiphyseal Dysplasia (MED) in August 2020. MED is a rare genetic disorder that effects the development of the joints in the legs. Her doctors recommended Nemours Children’s Hospital, Delaware to see orthopedic surgeon Dr. Will Mackenzie and orthogeneticist Dr. Mike Bober. […]

Olivia’s Story – Trisomy 18 Awareness Day

Brooke Renton’s life changed substantially when her daughter, Olivia, was born in March 2021, both in the physical sense (the family permanently relocated from Tallahassee to an Orlando suburb to be closer to Nemours Children’s Hospital, Florida) and in the emotional sense when she knew she would do anything for her sweet baby girl.   Born with a rare chromosomal condition called Trisomy 18 at a hospital in Tallahassee, Olivia had to be on a ventilator for the first 11 days of her life. The day before she was supposed to go home, doctors had to perform lifesaving CPR and place Olivia back on a ventilator. Olivia’s heart was “pouring blood into her lungs” due to a hole in her heart known as a ventricular septal defect. NICU doctors in Tallahassee told the family that Olivia would need a specialized center that performed advanced pediatric heart surgery to correct the issue. Due […]

Personal Trainers and Athletic Trainers: What is the difference?

Personal TrainersPersonal trainers are found in gyms, health clubs, and even online as fitness influencers. Their goal is to help the general public achieve their fitness goals. Their clients can range anywhere from beginners to body builders, and they usually require a fee. Personal trainers are a great resource for cardio exercises, weightlifting techniques, and nutrition advice. There is no degree required to be a personal trainer. However, many have certifications that allow them to evaluate their clients and recommend exercises and nutrition regimens. While personal trainers are a very helpful asset to a person’s health and wellness, their role differs greatly from athletic trainers. Athletic TrainersAthletic trainers can be found in high schools, colleges, orthopedic offices, physical therapy clinics, hospitals, professional sports teams, military sites, and even in corporate and industrial settings. They provide athletes of all ages with preventative services, emergency care, therapeutic interventions, clinical diagnosis, and injury […]

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 […]

Raymond’s Story (In Mom’s Words)

My name is Alex Gaudlap. Also known as Raymond’s mom. Our journey with Nemours Children’s Health started in the fall of 2017 when we relocated back to New Jersey from Camp Lejeune, North Carolina due to Raymond not hitting developmental milestones appropriately. The doctors down South assured me Raymond was fine, but my motherly instinct told me he wasn’t. From the moment we stepped foot into Nemours Children’s, I felt like our concerns were listened to. Raymond’s first appointment at Nemours was with a neurologist in the Deptford location. Since we were new patients and basically starting from the beginning with tests, she ordered a routine EEG. We never would have thought that his first test would give us answers, but it did. Raymond was diagnosed with a rare form of epilepsy; that gave us some indication to why he had a global developmental delay. After receiving the epilepsy diagnosis, […]

Rare Disease Day: Reynolds’s Story (In Dad’s Words)

On December 8, 2017, my wife Ashley delivered our twins, Reynolds, and Campbell. She gets all the credit. I didn’t do any of the heavy lifting. We always knew that Baby A was larger than Baby B, but we didn’t know why. And we had no idea that there were going to be complications at birth. The boys were born at 36 weeks via C-sections, immediately whisked away and taken to the NICU. Reynolds was eventually transferred to another NICU, while Campbell just needed a little more time to grow. So, Reynolds and I left Ashley and Campbell to go to a children’s hospital in Little Rock, Arkansas, where we ultimately spent 103 days in that NICU. He had airway issues. He had cardiac issues. He had GI issues. And throughout that entire time in the NICU, doctors knew that there was some underlying reason causing these issues, but no […]

Page 19 of 28

Page 19 of 28

Page 19 of 28