Nemours Blog - Page 10 of 33 - Powered by Nemours Children's Health System

Childhood Cancer Awareness Month: Marjorie’s Story

Born at 27-weeks, weighing 1 pound and 15 ounces, Marjorie spent her first two and half months of life in the NICU. Following discharge, she was seen at Nemours Children’s Health, Jacksonville for hip dysplasia and eye checkups. When she was 7 months old, Marjorie’s parents noticed her belly was very distended. It continued to swell quickly, so her parents brought her to the pediatrician. After an ultrasound confirmed a mass, the family was rushed via ambulance to Wolfson Children’s Hospital where she first met Dr. Gauger. “Following multiple scans and tests, we heard the words you never want to hear, ‘Your child has cancer,’” says Marjorie’s mom, McCall. “Marjorie was diagnosed with neuroblastoma 4S. She spent three weeks in the hospital and was readmitted for more chemotherapy before being discharged on July 11, 2015.” After discharging, Marjorie continued to be followed by her oncology team at Nemours Children’s. “Through […]

Aurelia’s Story (In Mom’s Words)

The day before we were admitted to Nemours Children’s Hospital, Florida, my daughter, Aurelia, had had a bit of a cough, a fever, and was vomiting. I took her to two different urgent cares, and they both told us it was just a virus, and she was fine. That night I slept in the bed with her because I was concerned about her fever.  In the middle of the night, she started having trouble breathing and her lips turned blue. We took her to the emergency room and she was transferred to Nemours Children’s. There, she was diagnosed with septic shock, pneumonia, and heart failure due to strep and human metapneumovirus. She was put on a ventilator but she still wasn’t getting enough oxygen, so she was put on ECMO to see if that would give her heart and lungs time to heal. An ECMO machine is similar to a heart-lung by-pass machine used in […]

When Despair Turns Into Hope – Rhavi’s Story

Discover a tale of hope and resilience as Gabriella faces the challenges of her unborn child’s medical condition, Gastroschisis. Guided by the compassionate care of Nemours Children’s Hospital and the expertise of Dr. Margaret Chou and Dr. Loren Berman.

An Extraordinary Journey with Down Syndrome: Arlo’s Story

Like many expectant parents, Arlo’s parents couldn’t wait to find out the sex of their baby. When Carlie was 12 weeks pregnant, they opted to get NIPT bloodwork done to find out as soon as possible. When their blood screening came back, Arlo’s parents were surprised to find out that their baby boy had a 98% chance of having Down Syndrome. “Of course, we were shocked,” says Carlie, “But knowing about our baby’s condition only helped solidify the fact that he was so wanted and so loved—extra chromosome and all.” “From the moment we got the phone call with our diagnosis, through the rest of my pregnancy and now, we have been beyond blessed with amazing doctors, nurses, and therapists,” says Carlie. “The Down Syndrome Clinic at Nemours has been a beautiful addition to Arlo’s village. We feel like they are truly there for us, not as just another patient, […]

From Concussion to Clarity: Sammy’s Story

In 2020 and again in 2021, Sammy had two serious falls, both caused by fainting. Each time, Sammy was told she just had a concussion. However, the second time, her symptoms never went away. “I had a horrible headache that never left, the light continued to bother me and I wasn’t able to focus on stuff the way I normally did,” says Sammy. “I felt very limited during this time. I played volleyball and it would affect my ability to play. Being outside under the sun would cause me to get lightheaded and feel pain. I couldn’t touch my head much and I rarely pulled my hair up, unless it was for a game. It was even hard to sleep at night because of all the pressure I felt.” While in an appointment with Dr. Leto Barone for a different condition, he asked Sammy about her concussion. As she explained […]

My Little Unicorn

Discover the touching story of baby Raegan, who overcame duodenal atresia with the heartwarming guidance of Nemours Advanced Delivery Program.

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 Trevor Disease: Hudson’s Story

While Hudson’s parents were out of town, his grandmother noticed that something seemed a bit off with his ankle. She thought it looked funny, bigger. When his grandfather agreed, and also expressed concern about his ankle, they immediately booked a doctors’ appointment for Hudson when his parents returned home. “I took him in thinking, ‘I don’t know what’s going on,’” says Hudson’s mom, Elizabeth. “He hasn’t complained about anything, doesn’t have any pain, he thinks he’s fine. But, let’s go get his ankle checked, just to rule anything out.” That’s when they first met pediatric orthopedic surgeon Dr. Joseph Khoury at Nemours Children’s Health, Lakeland. After his first examination, Dr. Khoury explained to them that Hudson had flat feet. This didn’t come as a surprise to Elizabeth as her husband also has flat feet. “He then went on to do an X-ray,” says Elizabeth. “He looked at the results and Dr. […]

Finally Home and All Together: Brendan’s Story

When Courtney was pregnant with her son Brendan, her physician noticed something was off. During an ultrasound, they discovered that Brendan had an enlarged bowel, which can be a sign of cystic fibrosis. When Brendan was born in November of 2022, he was immediately placed in the NICU. “This was already planned and why we delivered in the Advanced Delivery Unit at Nemours Children’s Hospital,” explains Courtney. “The team was remarkable. Dr. Chou and our nurse, Mo, made a nerve-racking delivery as easy and seamless as possible. It was nothing but a great experience, considering the circumstances.” At only a day and a half old, Brendan had surgery. “During the surgery, they found that a part of the bowel had twisted on itself, causing it to not function properly,” says Courtney. “That day, they removed 30 cm of bowel and started the use of a colostomy bag. Then we had a 6-week healing […]

Page 10 of 33

Page 10 of 33

Page 10 of 33