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Work Hard, Rest Hard, Play Hard: Sparsh’s Story

At just 21 years old, Sparsh has already achieved what many only dream of, inspiring and touching the hearts of millions across the globe. Born with Osteogenesis Imperfecta, a condition making his bones extremely fragile, Sparsh faces unique obstacles in his daily life. Unable to bear weight on his hands and legs, he navigates the world differently than other kids. It was Sparsh’s diagnosis of severe scoliosis at the age of 14 that led him to Nemours Children’s Health. During a routine checkup and X-Rays with his local orthopedic doctor, Dr. Thomas McPartland, the scoliosis was discovered. Conversations about spinal fusion surgery immediately began. “My scoliosis required me to rest often in my wheelchair or on my bed to relieve back pressure,” says Sparsh. “It severely affected my posture, which indirectly hampered the function of vital organs such as my lungs, which are important to my singing career!” Sparsh is […]

Associate Highlight: Suken A. Shah, MD

At Nemours Children’s Hospital, Delaware, Dr. Suken A. Shah, The Shands/MacEwen Endowed Chair of Orthopedics and Chair of the Department of Orthopedic Surgery, leads with expertise and unwavering dedication to improve the lives of patients. His professional journey is rooted in a commitment to medicine and determination to solve complex cases. Reflecting on his early career decisions, Dr. Shah notes, “I was drawn to surgery early on, particularly during my medical school years.” Exposure to orthopedic surgery and guidance from esteemed mentors set him on the path to becoming a pediatric orthopedic surgeon. Dr. Shah’s decision to specialize in orthopedics stemmed from a desire to restore function and mobility, particularly in pediatric patients, setting the stage for his impactful career. Critical thinking and collaboration are essential components of patient care for Dr. Shah. “The most rewarding aspects of our work are when we can help a child with a complex […]

Family Advocacy: How Cancer took Cameron to Chords and Capitol Hill

For Cameron Thackston, 17, what started as a pain in his foot in early 2023, turned out to be something much more serious. He and his mom, Alma, thought it could’ve been tendonitis, only his condition wasn’t improving. The sharp pains continued to the point where the family was forced to take a trip to the emergency room. After a few rounds of testing Cameron received the news. He was diagnosed with cancer. Mom was devastated. “I went into a panic,” she said. And Cameron?  How did he take the news? He had one simple question for the care team. “Is it curable?” he asked. “Yes,” they said. “Cool,” he replied. With his primary diagnosis being T-Cell Acute Lymphoblastic Leukemia, his mom admits she was scared. But the family only had one choice. Fight. After rounds of infusions and oral chemotherapy and hours spent on the Hematology-Oncology Floor at Nemours […]

A Dream Recovery: Avyn’s Story

At just four years old, Avyn was diagnosed with a severe 60º curvature of Early Onset Scoliosis. Her local physicians recommended Mehta casting, prompting her family to begin searching for the best pediatric orthopedic specialists in the nation. Their search led them to Dr. Joseph Khoury in Florida and Dr. Alec Stall in Texas. The decision to choose between these two esteemed doctors wasn’t easy, but ultimately, Avyn’s family placed their trust in Dr. Khoury at Nemours Children’s Hospital, Florida. “Avyn has been extremely resilient throughout her scoliosis journey,” says her mother, Sarah. Thanks to her treatments, Avyn’s curve progression slowed, allowing her to maintain her normal life, participating in athletics and daily activities with minimal discomfort. However, as she grew older, her family knew she would need a spinal fusion surgery at age 10. “We discovered Nemours when Dr. Khoury transferred from Shriners Tampa to Nemours Children’s,” says Sarah. […]

From Michigan to Florida: Kevin’s Story

Kevin’s healthcare journey began at just three months old when he was diagnosed with Neuronal Migration, Microcephaly, and Differentiation Muscular Hypertonicity. This diagnosis marked the beginning of a new chapter for Kevin and his family, as they worked through the complexities of his condition. Prior to finding care at Nemours, Kevin’s diagnosis affected every aspect of daily life. His mother describes a relentless cycle of hospital visits and treatments. “He missed lots of school, and family trips,” says Kevin’s mom. “We would wake up 7-10 times a night, he would never sleep because of pain and so much more.” However, hope and new experiences emerged when Kevin’s family discovered Nemours in November of 2023. After months of research, they made the life-changing decision to seek care at Nemours, leaving behind their home in Michigan in pursuit of care for Kevin. From the moment they stepped through the doors of Nemours, […]

Associate Highlight: Dr. Evan Graber, Endocrinologist

Meet Evan Graber, Pediatric Endocrinologist and Program Director of the Pediatric Endocrine Fellowship at Nemours Children’s Hospital, Delaware.  Dr. Graber completed his Pediatrics residency at Cohen Children’s Medical Center of New York and his Pediatric Endocrine Fellowship at Icahn School of Medicine at Mount Sinai.  He has been working at Nemours ever since and can’t imagine a better place to work. “I knew I wanted to work with children back as a teenage camp counselor.  My interest in science drove me towards medicine in college and being a pediatrician has been such a privilege and joy.  I could not imagine working with any other population of patients. Endocrine spoke to me during residency. It is a field where you can follow patients and their families from birth to young adulthood.  Many endocrine conditions are chronic requiring not only medical knowledge but a desire to address psychosocial issues as well.  You get to form a real bond with families and forming those relationships makes Endocrine such a fun specialty […]

RCDP Awareness Day: Elias’s Story

Brittany and John found themselves navigating uncharted waters when their son, Elias, was diagnosed with rhizomelic chondrodysplasia punctata (RCDP) type 1. RCDP is a rare skeletal dysplasia that affects the body’s ability to produce plasmalogens which are essential for cell structure and nervous system function. Their journey began with the unexpected—low amniotic fluid during Brittany’s induction with Elias at 37 weeks. What followed were suspicions of cerebral palsy, only to discover skeletal differences and cataracts as well. It wasn’t until Elias was ten months old that the diagnosis of RCDP was confirmed. Before Nemours Children’s Health, life for Brittany and John was a whirlwind of uncertainties and challenges. “Our main struggle before diagnosis & coming Nemours was feeding issues,” share Brittany and John. “First, we didn’t realize Elias had a rare form of dwarfism, so we weren’t sure why he wasn’t gaining weight. Second, he developed a bottle aversion at […]

Navigating Youth Mental Health

Dr. Monica Barreto highlights the importance of the mind-body connection and the vital role of parents in supporting youth mental health.

Associate Highlight: Erin Taylor

Erin’s path in healthcare began as an EMT and Paramedic working for a fire department. However, she had big dreams of becoming a flight RN one day. “While completing school for nursing, I had the opportunity to work as a civilian combat medic in Afghanistan where I was able to provide aid to our soldiers and fly,” shares Erin. “From there, I was able to get a job at Nemours Children’s Hospital, Florida as a Paramedic in the Clinical Logistics Center until I received my RN license. I then began working in the RN resource pool, allowing me to get experience in all units of the hospital. I developed a passion for pediatric and neonatal cardiac and used that strength and experience to allow me to join the Nemours Transport Team.” Through hard work and determination, Erin found her home at Nemours on the Critical Care and Transport Team where […]

Page 11 of 28

Page 11 of 28

Page 11 of 28