Guest Contributor, Author at Nemours Blog - Page 4 of 27

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Enjoying Each Moment: Alek’s Story

Alek is a courageous patient whose journey with severe kyphoscoliosis led him across the globe to Nemours Children’s Hospital, Delaware. Kyphoscoliosis is a dangerous condition that affects the spine. It causes an abnormal curve in two directions, side to side and front to back. It is a combination of two other conditions: kyphosis, which causes a severely rounded appearance of the back, and scoliosis, where the vertebrae form a curvature instead of being straight. Alek’s diagnosis unfolded in Poland in 2010 when he was a young boy. The road ahead seemed daunting as his condition gradually worsened. “Before starting treatment at Nemours Children’s, Aleksander’s condition was very bad,” shares his family. “He had trouble with breathing and couldn’t eat and walk. He lived in chronic pain.” It wasn’t until after a failed operation in Poland that Alek’s family discovered Nemours Children’s. Referred by their physician in Poland, Alek and his […]

A Journey With Craniosynostosis: Georgia’s Story

At 11 months old, Georgia has already shown incredible resilience and strength throughout her life. Diagnosed with isolated nonsyndromic unilateral craniosynostosis at 8 weeks of age, Georgia’s journey has been a whirlwind of medical appointments, treatments, and hopeful recovery. Karin and Edwin knew early on that something was different about their daughter, Georgia’s, head shape. They voiced their concerns during her 1-month and 2-month check-ups. At her 2-month appointment, the nurse practitioner conducted a thorough examination. It was then that they noticed an absence of the soft spot on the top of Georgia’s head. This was a critical moment for her family. Craniosynostosis is a condition where one or more seams between the bones in a child’s skull close too soon. This premature closure prevents the skull from growing properly and results in an abnormal head shape. If left untreated, craniosynostosis can increase intracranial pressure, leading to developmental problems, headaches, […]

Associate Highlight: Kimberly Shoe’s Personal Connection to Pediatric Endocrinology

Kimberly Shoe, APN is more than an Advanced Practice Nurse; she’s one of our stars in the Endocrinology Department at Nemours Children’s Hospital, Delaware. She’s been helping to nurture future generations of providers since 2004 at Nemours Children’s, but her connection to her work runs deeper than her job title. Diagnosed with type one diabetes at 5 years old, her journey has connected her on a personal level with her patients. A kid at heart, Kimberly supports patients facing diabetes or other endocrinopathies. She’s an advocate for the transformative power of community, championing diabetes camps, support groups, and family-centered care. Outside of work, Kimberly has a passion for fitness and exercise with a special emphasis on running in marathons and half-marathons. Grateful for advancements in diabetes technologies, she knows firsthand the role exercise plays in a child’s life and strives to give her patients the best strategies to live their […]

Mending the Smallest Hearts: Lottie’s Tetralogy of Fallot Diagnosis (In Mom’s Words)

Our precious newborn, Lottie was the cutest bundle of joy we could have ever imagined. At just weeks old, our pediatrician noticed a heart murmur at her routine visit. We had no idea until a visit to the Nemours Children’s Cardiac Center in Delaware that she had any cardiac issues whatsoever. After an echocardiogram, Lottie was diagnosed with Tetralogy of Fallot (TOF). Her diagnosis included TOF with valvar and subvalvar pulmonary stenosis, with large secundum ASD and additional posterior muscular VSD.  After we received Lottie’s diagnosis, we were very anxious, knowing our child could have “TET spells” a condition where she would have had lack of oxygen and blood to her organs, including her brain. Constant monitoring and always watching for any signs, knowing that her condition was inevitably going to worsen. As a nurse, I knew immediately she would need open heart surgery and I felt like my whole world came […]

On The Right Path: Marina’s Story

When Marina was just 6 months old, her family noticed something unusual—her neck often fell to one side. This seemingly minor issue led to a series of medical consultations and diagnoses that would shape the future for Marina and her family. Diagnosed with torticollis and abnormally low muscle tone (hypotonia) by her pediatrician, Marina was referred to a neurologist at Nemours Children’s Hospital, Florida for further evaluation. Upon consulting with Nemours Children’s specialists, it was discovered that she was experiencing frequent seizures. “Various specialists conducted studies, leading to the discovery of congenital cytomegalovirus on February 2, 2022, just after her first birthday,” shares her mother, Kenialys. “This news left us shocked, confused, sad, anxious, and scared. However, the dedicated care from healthcare professionals at Nemours helped us regain optimism and hope for Marina’s future.” Cytomegalovirus (CMV) is closely related to the viruses responsible for chickenpox and mononucleosis (mono). Babies infected […]

Navigating Crohn’s Disease: Billy’s Story

Jessica, 12-year-old Billy’s mother, recalls the summer of 2022 when they noticed something unusual during their family getaway. “While on vacation, we discovered he had an anal fistula,” she recounts. In April of the following year, Billy experienced his first flare-up, ultimately leading to a diagnosis of Crohn’s disease. Located in their hometown, Nemours Children’s Hospital, Florida became a regular visit for Jessica and Billy. “We have lived in Lake Nona for over 11 years,” says Jessica, so they were already familiar with the Nemours Children’s location. From the moment they stepped through the doors, they were greeted by a team of dedicated professionals led by gastroenterologist Dr. Pablo Palomo. Reflecting on their experiences with the Nemours team, Jessica highlights the genuine care and compassion in each interaction. “Billy’s liked everyone he’s ever interacted with,” says Jessica. “My favorite thing about them is how special they make me feel, even […]

From Diagnosis to Triumph: Ny’Jour’s Journey

From diagnosis to triumph, Ny’Jour’s complex medical journey involving heterotaxy and heart complexities received compassionate care from Nemours Cardiac and Maternal-Fetal Medicine teams.

AMC Awareness Day: Sara & Ewa

On this Arthrogryposis Multiplex Congenita (AMC) Awareness Day, we shine a spotlight on two remarkable women, Ewa and Sara, whose journeys with AMC have inspired countless individuals. Ewa’s journey with Nemours Children’s Health began in 1986 when she traveled from Poland to receive treatment for AMC, a rare condition affecting 1 in 3,000 births. Nemours became her second home, offering life-saving care and support from a dedicated team of doctors and therapists. “Nemours, along with my family, truly shaped me into the person I am today,” Ewa shares. Her gratitude for the care she received has fueled her commitment to give back through various fundraising initiatives, including Nemours Radiothon, Brace for the Race, and an annual toy drive. In her latest endeavor, Ewa organized a book fundraiser for another Arthrogryposis patient and author, Sara Gaver. For every book donated, Ewa matched the donation, resulting in a collection of 110 copies […]

Scoliosis Awareness Month: Esther’s Story

Esther’s journey with scoliosis began during a routine check-up in the summer of 2020. Her primary care physician discovered the curvature of her spine during a yearly visit, just as Esther was experiencing a growth spurt. Her provider quickly referred Esther to a specialist at Nemours Children’s Health, Jacksonville, where an X-ray confirmed the diagnosis. “I went to get X-rays and found out my spine was crooked,” Esther shares. “It was unexpected, but I’m grateful we caught it when we did.” Under the care of orthopedic surgeon Dr. Kevin Neal, Esther embarked on an 18 month journey, closely monitoring the progression of her curve, and exploring treatment options. In the beginning, Esther didn’t experience much pain. However, as the curvature of her spine progressed, approaching 60 degrees, the impact on her daily life became increasingly challenging. “Pain didn’t come until the curve progressed horribly over two years or so, and […]

Associate Highlight- Jonathan Haro’s Stem Cell Donation

Jonathan decided to become a nurse after his grandfather was diagnosed with bladder cancer. He was inspired by the many great nurses that cared for his grandfather at home and inpatient. Around the time he was graduating high school he was thinking about careers to pursue. Jonathan says, “I knew I liked working with people, and most of all I liked helping. Nursing fit into those categories perfectly and that’s what led me to apply to nursing school.” But Jonathan’s story here at Nemours Children’s Health is unique. Here’s his incredibly unique journey in his own words: In April of 2023, I was running in the Mimosas for Marrow 5K that is hosted by a previous oncology patient and her family. At this 5K I connected with the National Marrow Donor Program (NMDP), who added me to the national donor database. In November, I then found out that I had […]

Training the Next Generation of Pediatric Mental Health Providers:

Fellows Share Their Challenges and Triumphs  For Mycah Ayala-Brittain, volunteering in her mother’s special education classroom was her first opportunity to learn how professionals collaborate to meet the needs of children. The classroom had teachers, teaching assistants, physical therapists, occupational therapists, speech and language pathologists, and medical personnel that collaborated to provide individualized care to support children with behavioral health needs.   Throughout her education, Mycah learned about the barriers that families face accessing quality health care. These experiences led her to pursue a doctorate in psychology, expanding her knowledge and allowing her to provide culturally sensitive mental health care. At Nemours Children’s Health, Mycah has had the chance to explore multiple behavioral health settings, further growing and strengthening her skills within an integrated health care system.   When Martisha Brown was growing up in Delaware, she felt like she didn’t have the counseling support she needed. High school brought about challenges, […]

Scoliosis Awareness Month: Kalani’s Story

Under the expert care of our dedicated team in Nemours Children’s Hospital, Florida, Kalani embarked on a path of treatment for juvenile idiopathic scoliosis and neurofibromatosis type 1 (NF1) at 6 years old. Her journey began in July 2023 when her mother, Monica, noticed a slight curvature in Kalani’s back. Concerned, they sought answers from orthopedic surgeon Dr. John Lovejoy at Nemours Children’s. “An X-ray confirmed that her back had a curvature and an MRI was ordered out of caution to make sure there was not an underlying issue causing the curve,” shares Monica. “The MRI showed she had lesions/tumors believed to be caused by NF1. Following the MRI results, Dr. Lovejoy referred Kalani to oncology and genetics to confirm the diagnosis and begin treatment. When we had a follow-up with Dr. Lovejoy at the end of October 2023, an X-ray showed the curve in Kalani’s spine had gotten worse […]

Page 4 of 27

Page 4 of 27

Page 4 of 27