The path of a child living with cerebral palsy (CP) is filled with emotions, obstacles, and decisions. Gillette Children’s researched what influences parental decision-making to offer enhanced support to patient families.

The 2023 Orthotic & Prosthetic Innovative Technologies (OPTech) Conference in Minneapolis brought together more than 130 experts and professionals from around the country to discuss the latest and contemplate future advancements in orthotic and prosthetic technologies. 

Gillette Children’s is well represented as hand surgeons and upper limb difference specialists from six continents and 37 countries gather in Minneapolis for the 2023 World Symposium on Congenital Malformations of the Hand and Upper Limb. Gillette orthopedic surgeons, Ann Van Heest, MD and Deborah Bohn, MD, are presenting research and sharing their new book "Proud to be Me."

Rewaa Elgazzar begins nine-month role as Rare Disease Diversity Coalition (RDDC) Research Fellow at Gillette Children's.

Gillette Children's is known worldwide for its expertise in caring for children diagnosed with rare diseases. Gillette complex care pediatrician, Arthur Beisang, MD is part of the team devoted to providing excellent care and improving the lives of children living with a rare disease.

Gillette Children’s has a comprehensive team of pediatric neurologists to help parents and guardians understand the common causes and signs of seizures in children. These Gillette specialists work with families and primary care providers to ensure children get an expert, first seizure evaluation and a treatment plan if it’s needed.

Gillette Children’s conducts clinical research every day to answer some of the most important questions for patients and families. We focus on improving treatments and making life better for children with medical conditions or disabilities.

From fashion advice to practical tips for skin irritation, we answer the common questions kids and teens have about wearing scoliosis bracing.

For 125 years the doctors, nurses and employees at Gillette have worked every day to provide the very best care for all children. This dedication has led to treatments and outcomes that have influenced cerebral palsy care worldwide. 

Rare Disease Day is Feb. 28. The main objective of the day is to raise awareness about how rare diseases have an impact on people’s lives and our communities. Gillette Children's is known worldwide for its expertise in caring for children diagnosed with rare diseases such as Rett syndrome, spinal muscular atrophy (SMA), acute flaccid myelitis (AFM), Legg-Calve Perthes disease, Prader-Willi syndrome and other conditions.

Augmentative and Alternative Communication devices are part of a child's communication system, ranging from choice boards to iPad apps.

March is National Cerebral Palsy (CP) Awareness Month and Gillette Children's is one of the world’s leading centers for cerebral palsy diagnosis, treatment and research. We enhance the lives of individuals who have cerebral palsy and are advocates for CP patients and research.

Figuring out if your child has a rare disease is a concerning and challenging puzzle for parents.Two members of the Gillette team, pediatric neurologists Randal Richardson, MD, and Jamie Eskuri, MD, say finding answers and guiding families through a rare disease diagnosis and care plan is one of the most rewarding parts of their jobs.

At the 2021 Annual Meeting of the International Perthes Study Group (IPSG), organizers announced that Gillette is second in the world in its enrollment of Perthes patients into IPSG studies.

The ability to stand up straight is something that most of us take for granted. Peyton's family can tell you how the ability to stand upright, transformationally changed her view of the world. Read more about the surgery that made it possible.

The U.S. Food Drug Administration’s (FDA’s) recent approval of a new oral medication to help treat spinal muscular atrophy (SMA) is being hailed as a “game changer” by Gillette Children's neurologist, Randal Richardson, MD, MMS. “The main message I want to get out to people who have SMA and their families is—many of you now have options and the power to make a choice for yourself,” Richardson says.

Toren Theiss is 11 years old. He’s an incredibly active young man who plays soccer, ski races and though he wouldn’t brag about it, does quite well at both. It wasn’t until a day in August two years ago when he was walking towards his mother Jill, that she realized something was wrong.

With her shock of blonde hair blowing in the wind, Mari laughs while flying down the trails on her mountain bike and has aspirations to conquer the monkey bars at her local playground. These athletic feats become all the more impressive when you consider the fact that Mari was born missing nearly all of the fingers on her right hand.

“It’s just so wonderful to watch these children get better. It’s also very rewarding to see the connection that forms between the children and my dogs. They become friends.”

The hospital can be a scary place for anyone, especially a child, and no matter how nice the staff is or how thoughtfully the clinical spaces are designed, it’s usually difficult for a patient to forget they’re in one. At Gillette Children’s, that’s no longer the case.

The day was Christmas Eve, the year was 2003 and the Ketelhohns were resting and watching a movie in their home near Milwaukee, Wisconsin. It was an idyllic evening, but their youngest daughter, 8-month-old, Kate, had a slight fever. It was the type of malady that many children experience throughout their development. There was no reason to worry, until there was.