Gillette has one of the nation’s only sleep medicine programs specifically designed for people who have disabilities or other complex health conditions. The American Academy of Sleep Medicine (AASM) reports the Gillette Sleep Health Clinic is one of the most well-run sleep labs its surveyor has ever reviewed. The AASM recently awarded Gillette a five-year re-accreditation.

Gillette Children’s Specialty Healthcare is one of 15 institutions across the U.S. being honored with International Rett Syndrome Foundation (IRSF)’s Center of Excellence designation or redesignation

When I was 2 years old, I was diagnosed with cerebral palsy. Now, I'm 23. I've faced many challenges in my life, but I think my dad said it best, "Inch by inch, life's a cinch. Yard by yard, life's hard." You can't get too caught up trying to project what the end result might be, all you can do is try to deal with the challenge in front of you, and move forward.

When COVID first came to Minnesota and things started shutting down, we were concerned that our son, Wes, who is 8 Years old and has cerebral palsy, would not get the care that he would need. But that hasn’t been our experience.

March is National Cerebral Palsy Awareness Month. Gillette Children’s Specialty Healthcare is the world-renowned leader in the treatment of cerebral palsy. We enhance the lives of individuals who have cerebral palsy and promote their well-being by improving diagnosis, management, and care through research, innovation, and collaboration. The Harkness family shares their story of why selective dorsal rhizotomy (SDR) surgery at Gillette was the best choice for their daughter.

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.

January is National Winter Sports Traumatic Brain Injury (TBI) Awareness Month. Prevention and precaution are the keys to staying safe and minimizing injuries. If your child does become injured the team at Gillette Children's Specialty Healthcare has a higher level of training to deal with pediatric TBIs.

The Quinn family shares their experience about their newborn daughter receiving a diagnosis of craniosynostosis. They appreciate the Gillette team approach to care which allows for collaboration between the neurosurgeon and the plastic surgeon to formulate a clear, patient-specific plan. Two surgeons working side-by-side in the operating room decreases operating time and reduces the length of exposure a child has to general anesthesia.

Peter Kim, MD has worked as a Pediatric Neurosurgeon at Gillette Children's Specialty Healthcare for nearly ten years. Dr. Kim assumed the role of Associate Medical Director for Surgical Services at Gillette in 2021. Kim has been with Gillette since 2011 and has extensive expertise in treating Chiari malformation, epilepsy and seizures, tethered spinal cord, spina bifida, craniosynostosis, and hydrocephalus. Learn more about him, here:

Going sledding is ridiculously fun, but it can also be dangerous. Wearing a helmet makes it safer.

For families like Colton’s, the costs of care can be overwhelming. That’s why our donor-funded Gillette Assistance Program exists—to help families worry less about finances so they can focus solely on their child’s care. Not all heroes wear capes, but you can become a hero for kids like Colton when you support Gillette with your donation today. 

A new pediatric neurologist at Gillette Children's Specialty Healthcare discovered a passion for her field while eating a slice of pizza. Jamie Eskuri, MD, is excited to begin working with Gillette families and to be back in the state she considers home.

A diagnosis of epilepsy can be a confusing time for a family and child. November is Epilepsy Awareness Month and Gillette Children's Specialty Healthcare wants to remind families we're a source for expert diagnosis, treatment and support of people who have epilepsy.

George Jamison clearly remembers the moment. He was with his older brother, Jack, at summer camp, having the type of fun that only 8 and 10-year-olds can. Then everything went black. When he awoke, a lot had changed.

October is Spina Bifida Awareness Month as well as National Bullying Prevention Month. Most people have experienced some form of bullying during their lives, but unfortunately, many children who have disabilities experience this much more acutely. Earlier this year Gillette patients, Chloe and Gracie sat down to talk about the care they received at Gillette. They also touched on some of the bullying they dealt with at school along the way.

Owen Nei is 11 years old, an avid hockey and baseball player, and a young man who lights up every room he’s in with his positive, irrepressible attitude. Given how his life started out, the fact that he’s even here, much less doing all of these things, is nothing short of a miracle.

October is Spina Bifida Awareness Month and October 25 is World Spina Bifida and Hydrocephalus Day. To recognize the day and the month, we're sharing the story of Chloe and Gracie, two longtime Gillette patients connected by spina bifida, but much more than that, their profound friendship. Read their story here.

Spina bifida is fairly common, occurring in one of every 1,500 births, and is a complex condition that requires a team of experts to make sure each child can thrive. A team of Gillette specialists, including neurologists, orthopedic surgeons, urologists, rehabilitation medicine specialists, therapists, psychologists, social workers, and orthotists is ready to help parents and referring providers create a treatment plan especially designed for each child diagnosed with spina bifida.

Gillette Children’s Specialty Healthcare is ready to help as the Centers for Disease Control and Prevention (CDC) warns that 2020 could be another peak year for cases of acute flaccid myelitis (AFM)—an uncommon but serious neurological condition that mostly affects children. The polio-like condition tends to peak in the fall months every other year. The last surge of AFM was in 2018 where more than 200 cases were diagnosed across the U.S., according to the CDC.

At Target Field, every Sunday is Kid’s Day and on a beautiful summer day in August of 2019, Samuel Anastos scored the first honorary run of a Minnesota Twins game. It was a joyous moment made all the more meaningful because there was a time in Sam’s life when his parents questioned whether he would learn to walk or talk, much less run.

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 Specialty Healthcare 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.

The Centers for Disease Control and Prevention (CDC) is warning parents and medical professionals that 2020 will be another peak year for cases of acute flaccid myelitis (AFM) a rare, polio-like neurological condition that affects mostly children. Gillette Children's Specialty Healthcare is ready to be an important center for AFM care and rehabilitation when the outbreak is set to peak this fall.

In all the ways that matter, Peter is your typical 8-year-old. He’s a protective older brother to his younger sister Katie, loves cars, sports and Star Wars. He’s easy to smile, quick to laugh and brings joy to all who meet him. When you’re in Peter’s presence, the fact that he has cerebral palsy and can’t speak, quickly becomes an afterthought.

Matthew suffered a traumatic brain injury 15 years ago. After the treatment at Gillette that saved his life, he’s had a singular goal: To live every day, better and stronger. As he says, “It’s not about what I lost, it’s about what I’m getting back.”

Many families and providers are taking advantage of the newly expanded virtual care appointment options at Gillette Children’s Specialty Healthcare. During the “stay at home” orders due to COVID-19, Gillette continues to focus on ensuring families are safe and have access to our expert medical care.Pediatric neurologist, Randal Richardson, MD, is seeing patients via virtual care, when clinically appropriate, and he's excited about how technology makes it more convenient for his patients.

“It’s not an exaggeration to say deep brain stimulation (DBS) surgery at Gillette changed Sam’s life,” marvels his mother Coleen Wedig. Sam Wedig, 16 and his mother first traveled to Gillette Children’s Specialty Healthcare from Des Moines, Iowa in 2015 seeking help for cerebral palsy and dystonia. They’re passionate about sharing their story in the hope they can help other families dealing with similar medical challenges.

"Every step Sophia takes is a testament to the countless dedicated individuals who made it possible," says her mother, Susan Slinkard. Sophia and her family traveled from Arkansas to Minnesota for several major surgeries aimed at reducing Sophia's spasticity.

As loud music filled the adjoining hallways near the Neurosciences unit at Gillette Children’s Specialty Healthcare, passersby could be forgiven if they were a bit confused. The atmosphere was festive and there was good reason for it. At long last, James Bostic, 17, was able to go home. He had been in the hospital for 15 months.

There are few moments in life as exciting and anxiety inducing as the day you have your first child, but for Andrew Bailey and his wife, Amanda, things were a bit more complicated. Amanda was home in Connecticut getting ready for her baby shower. Andrew, a pitcher for the Boston Red Sox, was in Seattle for an away game.

When Jenna Robinson was born, she only weighed three pounds and doctors told her parents she’d never be a “rocket scientist.” Now 28, she holds a Master’s degree in social work and has dedicated her life to helping individuals lead more independent lives.

Wes Jackson is a thoughtful, kind and inquisitive kid. He also has cerebral palsy, but he won't let that (or anything else for that matter) get in his way. Get to know Wes and his family, you'll be glad you did.

Laney and Lilah are feisty, happy twin sisters. They share a diagnosis of cerebral palsy, but that is just one aspect of their lives. More importantly, they dance, they laugh and occasionally throw things.

Every now and again, I write a new letter to my son, Landon. It’s my testament to him. To who he was, to who he is, and to who he could someday be.

“Knowing that Gillette is a PPMD-certified Duchenne Care Center means the world to us because we know for certain Tyler’s getting the specialized care that he needs," says his mom, Marilyn. Meet Tyler and learn about his family's "game plan" to tackle Duchenne muscular dystrophy.

Louie Romero is a smiley kid that simply can’t help the fact that he is irrepressibly charming. It's Louie's personality that makes an impression when you meet him. The fact that he is in a wheelchair and has cerebral palsy ranks much lower on the list.

As he ambles down a long hospital hallway, smiling with every step and practically daring you to do the same, it can be pretty easy to forget that this wasn't supposed to happen. Mateo Arcos was never supposed to walk.

Your brain isn't like your arm. You can’t see it or touch it. It’s not really tangible, which means that we rarely spend time thinking about the thing that makes us think, unless we have to. This is what those who experience a TBI go through.

“I’m always amazed at just how strong and brave they are,” says Laura of her sons Collin, 7, and Simon, 4. These sweet and exuberant brothers both received a diagnosis of hydrocephalus at age 1 and see Patrick Graupman, MD, for treatment.

Tall, red-haired and boisterous, it’s not a surprise to learn that Connor plays on the football team back in North Dakota, or that he’s pretty popular.

"If there is anything that I want people to understand, it’s that parents who have children who have disabilities want what any parent wants for their child."

Kiara and Keisy are twins who share a diagnosis of muscular dystrophy. Meet these sweet girls and learn how their parents, and Gillette, help them understand they're no different than other kids.

There are few things in life as overwhelming as learning your child has a disability. Accepting this and moving forward is a different process for every parent. We spoke with Gillette neuropsychologist Richard DiPrima, PsyD, and below he offers advice to help families navigate this emotional time.

Small, gregarious, brimming with boundless energy and a mischievous smile, 4-year-old Emmy Veenis is the type of kid people tend to remember. But Emmy started having headaches.

Gillette recently hosted a Facebook Live video Q&A featuring John Garcia, MD, sleep medicine specialist, about back-to-school sleep issues. Learn more and watch the discussion.

Colten's family thought he'd come down with the stomach flu. Then his illness became something much more severe. Learn how a Gillette pediatric neurologist and Colten’s rehabilitation team helped him reclaim his childhood.

A Gillette physician is cautioning those who are traveling to the Olympics in Rio to take extra care and precautions due to the Zika virus’ prevalence in the region.

The arrival of the Zika virus in the U.S. has raised awareness of the hidden risk of viruses, particularly those that cause problems for pregnant women and their babies. Zika, however, is only one of several viruses and conditions that can have an adverse outcome on a child in the womb.

A few simple tips, such as wearing a helmet and taking breaks, can help kids stay safe outside during the spring and summer months.