Gillette Children's is expanding its craniofacial services to Duluth to offer families in northeastern Minnesota convenient access to expert care. On the fourth Monday of every month pediatric craniofacial and plastic surgeons, Jo Barta, MD and Courtney Carpenter, MD, will have appointments in Gillette’s Duluth Clinic.

Joslyn Jane Rogers is a cheerful, enthusiastic 11-year-old. She has many interests including reading, gaming, swimming and baseball. Joslyn also has cerebral palsy (CP) and she's been a patient at Gillette Children’s since she was 1. 

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.

Join Juan Diego and his team for Gillette Children's 2022 Walk & Roll community and fundraising event on September 24!

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.

Two mothers share their journey of receiving cleft lip and/or palate care for their babies at Gillette Children's. July is National Cleft and Craniofacial Awareness Month. Gillette has one of the largest craniofacial programs in the U.S. Both mothers appreciate the expertise care and support at Gillette. You can see by her smile that Heavenly Smith is delighted with the outcome. 

At Gillette Children’s, it’s our mission to help every child reach their potential and achieve the independence and agency to create their own story.That’s why we celebrate Disability Pride Month, and we hope that you'll join us.

You know, there might be nothing more Minnesotan than lacing up a pair of skates and heading out to the rink. “You bet, you’d better believe it,” says Tony Lang of Loretto, Minnesota. “I grew up playing hockey my whole life. It’s a family tradition. In fact, when we had kids I built a rink in our backyard.”

Born missing her arms, Ruth Evelyn (RE) can do pretty much anything using her feet. But she's always dreamed of riding a bike. So her family turned to Gillette to help make her dream a reality.

April is Occupational Therapy (OT) month and Gillette is highlighting the amazing work our OT team does every day to help our patients increase their independence with daily activities. Gillette is one of the only pediatric health care centers to have an ArmeoSpring machine. Our occupational therapists use this robotic exoskeleton to assist patients who are building strength as the result of trauma, cerebral palsy, neuromuscular conditions or stroke.

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.

"Every step Sophia takes is a testament to the countless dedicated individuals who made it possible." Sophia and her family traveled from Arkansas to Minnesota for several major surgeries to treat her cerebral palsy.

Bubbles, books, and stuffed animals are tools of the trade for child life specialists at Gillette Children's. March is Child Life Month and a time to highlight the joy and hard work these health professionals bring to hospitalized children and their families. When you come to Gillette you’ll collaborate with child life specialists who have extensive knowledge of child development and are experts at understanding how a medical environment can affect children.

The 12th Annual Gillette Children's Adaptive Ski Day was an opportunity for children who have disabilities to discover the thrill of downhill skiing. Marcie Ward, MD, is a Gillette pediatric rehabilitation medicine physician and says these adaptive sports events bring joy and can transform children and families.

“The Everybody Club” is a book about love. It easily could have been a book about grief, heart break and the struggles in life. But that’s not what author Linda Hayen and her daughter Carissa wanted to put into the world. Linda Hayen, is the mother of a Gillette patient and says it's joyful, colorful story about inclusion that's based on the relationship between her daughter and son.

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

I have always said that the only thing that I want for Peyton is for her to be able to “create her own story.” I want her to tell us what she is capable of doing and not let anyone believe less of her.

Caleb Binkert wrapped up a preholiday evening shift as a cashier at a Target in Vadnais Heights, Minnesota on November 6, 2020. He put on his bike helmet, his reflective clothing and started biking home around 9:30pm. Caleb, 17, does not remember anything from that day as he rode through a crosswalk to continue his journey home. In an instant his life changed.

Aaron Navarro is a teenager from Grandview, Texas. He's an active member of his high school debate team and runs 5K races (even though he’ll tell you that running isn’t his favorite thing). His mother, Christine, will tell you that the fact that he is running at all is nothing short of remarkable.

Today we're sharing the story of Chloe and Gracie, two longtime Gillette patients connected by their shared condition of spina bifida, but much more important than that, their profound friendship. 

The emotional stories, the positive energy and people pulling together for a great cause are all part of this year’s KS95 for Kids Radiothon at the Mall of America on Dec. 10. This on-air radio fundraiser benefits Gillette Children's and M Health Fairview University of Minnesota Masonic Children’s Hospital.

After Jeffrey received an intrathecal baclofen pump that would help manage his cerebral palsy at Gillette, his world opened up. He inspired his dad to become a marathon runner and even became an official "marathon maniac" in his own right.

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.

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

ZaLayaa Wandrick is 9 years old. She’s an excellent cook, crafter and loves science, soccer and coding, but for much of her life, has had to deal with multiple sensory and complex medical conditions. Since her infancy, Zalayaa has endured a variety of different symptoms that have impacted her daily life, but perhaps the most frustrating thing about all of it has been that the underlying cause of these issues remained a mystery.

Harrison Clausnitzer from Lakeville, MN is a 5-year-old bundle of joy and is the ambassador for the 2021 Walk and Roll to raise money to support Gillette Children’s. Every dollar raised during the event supports Gillette’s mission ensure every child can reach their full potential.

To see Taylor ride her horse is a study of grace in motion. That she's doing it after treatment for juvenile idiopathic scoliosis, makes it even more impressive.

In just over a month, Kyra Condie will be competing as a climber in the Summer Olympics in Tokyo. It will be the first time climbing has been featured as an event in the Olympics and for her, a tremendous personal achievement and milestone she’s been working towards her entire life. A diagnosis of scoliosis could've made this feat unattainable, but her personal dedication and the treatment she received at Gillette made it possible.

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 I work with my patients at Gillette, I try not to impose my story and my “why” on them and their families. But inevitably, it comes up. My younger brother, Peter has cerebral palsy. He’s why I do what I do and why I’m here. I’m immensely proud of him and grateful to have had the privilege of being his sister.

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.

Ethan Johnson was diagnosed with a rare condition as an infant. His parents were told he may never walk without assistance. Now seven years old, not only does he walk, he flies out on the ice. Read Ethan's story here.

When Isabella Gregory, 11, received a diagnosis of juvenile idiopathic scoliosis in 2019, it was a shock to say the least. Read about the unique surgical procedure that got Isabella back to her life and activities just 6 weeks later.

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.

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

Most parents would tell you that having a child changes your life in ways you never could have imagined. That certainly was the case for my husband, Mike and me. Our daughter, Peyton, is now 9 years old, and it’s been a journey of hope, faith and love.

In a time where many may feel disconnected, the providers at Gillette Children’s are going out of their way to remind our patients and their families that we see them and that their inclusion matters. This is happening in a variety of ways, but let’s start with a girl named Mari and her new doll.

Like so many of our favorite events, the 2020 KS95 for Kids Radiothon will look a little bit different this year – but the switch to a fully-virtual Radiothon means that there are even more ways to show your support!

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.

"Grady’s so much more than his condition. The way we see it is that God gave us this incredibly cool kid who’s had to deal with a few things. We've had challenges, but life is good even when stuff is hard. Either way, because of Gillette and the care they provide, Grady's future will be whatever he decides it to be. That’s no small thing.”

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.

Speak Now for Kids Week is a public platform for citizen advocates to learn, get involved and influence the outcomes of current child health policies. This year, three Gillette families met with representatives from the Minnesota Congressional Delegation to advocate for kids and Children's Hospitals.

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.

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 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.

When virtual appointments were first proposed, we were appreciative but admittedly skeptical about how that would work. But having recently made the shift over to virtual appointments, we’ve been pleasantly surprised by how seamless the transition was. Naturally, there were some growing pains in the beginning, but there were many benefits that emerged over time.

Joe Carr is a socially connected doer and thinker so a worldwide COVID-19 pandemic was not about to stop him from launching his 5th annual Lemonade Stand Fundraiser for Gillette Children's. In fact, Joe and his team say in a strange twist COVID-19 might make this year of fund raising even more successful.

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.”

"It was definitely a shock. I almost didn’t believe it at first. I’m a competitive athlete; I’d never really been hurt or sick in my entire life. I didn’t even know what scoliosis was." - Avery Wright

"I realized, for the first time, that I was shooting straight. Due to my scoliosis, I'd been overcompensating." Erika, a basketball player, gained confidence after surgery to correct her spinal curvature.

Gillette Children's has launched a new resource to help parents of children who have complex, rare or traumatic conditions. The first book released by the new Gillette Children’s Healthcare Press is Spastic Diplegia—Bilateral Cerebral Palsy and it’s written by Lily Collison, an Ireland-based author and the mother of a Gillette patient.

The outbreak of COVID-19 is an unprecedented crisis that has disrupted the lives, schedules and daily routines of millions across the globe. This is a difficult time and we know that our patients and families are going through many transitions simultaneously right now. At Gillette Children’s, our number one goal is keeping you and your family safe. To help during this time, we’ll be offering virtual appointments via video whenever possible and clinically appropriate.  

“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.”

After enduring a ruptured aneurysm, doctors told Trevor's parents were told he'd never walk again. After a six-week rehabilitation stay at Gillette Children's, Trevor strode out of the hospital doors - walking independently.

As loud music filled the adjoining hallways near the Neurosciences unit at Gillette Children’s, 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.

Nicole Leinonen says she’ll never forget the phone call that she says changed her life. “Every time I think of that phone call from Gillette telling me that I qualified for some financial assistance I get emotional. I’m amazed at how generous people are,” Nicole says. “The Gillette Assistance Program (GAP) means I can focus on Ella and her needs. I don’t have to be so stressed worrying about how, as a single parent, I can pay for her care.”

Learn about how Jennifer and her son Nick, a Gillette patient who has cerebral palsy and epilepsy, came up with an idea for a part-time business making dog treats and turned it into a reality that they hope will provide employment opportunities to other young adults who have disabilities.

Seven-year-old Maria Renata Sanchez Diaz traveled 1,600 miles from her home in Mexico City to Gillette Children’s as part of her plan to keep a promise to her dad.

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.

Charlie Schultz is a longtime Gillette patient, athlete, and most importantly, a dog lover. Learn how Charlie's love of dogs blossomed (and led to him becoming a dog owner!) during his seven-week inpatient stay to treat his severe spinal curvature, called kyphosis.

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.

Mason is a happy five-year-old with a contagious smile and a laugh that brings a smile to your face. Diagnosed with cerebral palsy, Mason has attended Gillette for occupational, physical and speech therapies to help him strengthen his muscles and vocal skills. Learn how Mason and his family are showing their gratitude for Gillette this summer!

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.

For Janet Favorite, navigating her son Robert’s rare condition has been a rollercoaster, steadied by her family’s commitment to providing him with expert care and access to resources at Gillette Children’s. Read her story here.

Rolling over, crawling. The first words, the first steps, the first bike ride. These actions seem small individually, but many serve as formative moments that represent individual progress. They’re the signs that we’re moving forward and the experiences we remember. However, for many of the patients and families at Gillette Children’s, these milestones are often delayed—if they happen at all.

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.

Cassidy and her mom, Darcy, are two of the biggest fans of the University of Minnesota women's volleyball team. They're excited about the NCAA Division I women's volleyball tournament at Target Center in Minneapolis. While they're disappointed the Gophers will not appear in the NCAA tournament, they're proud of what the team accomplished this season. Cassidy has quadriplegic cerebral palsy and her limited use of her arms and legs means is can be difficult to stand and cheer for her team--until Gillette helped make her dream come true.

The human body is a miraculous makeup of coordinated and interconnected systems that, when operating properly, are a wonder to behold. But when things aren’t operating correctly, this interconnectedness can cause a whole host of complications. This issue is precisely why Gillette’s Aerodigestive Clinic was established last year.

Hope is many things, including an animal-lover, a peacemaker and a big sister. She's also a longtime Gillette patient, where she receives treatment for multiple pterygium syndrome, a condition she shares with her dad.

It's rare for a singular event to bring so much joy and meaning to so many individuals and organizations, but Gillette Children's celebration of the 3rd Annual Mauer and Friends Kids Classic, did just that. The event took place on a perfect, June day, and 25 Gillette patients and their families had the experience of a lifetime down on the grass of Target Field.

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.

After moving from small-town Iowa to the Twin Cities to be nearer to Gillette, Bentley’s parents describe him as a whole new child. He’s talking, reading and thriving in kindergarten, where his classmates exude kindness.

“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.

Parents worry. Parents worry about their child’s growth, development, friends, school, future. It’s a universal truth, baked into our biology. When a child is diagnosed with special needs, however, a parent’s worry can snowball into anxiety. That's what happened to me, but here's what I did.

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.

Not one to sit on the sidelines, Danny Lilya’s wheelchair and congenital spine diagnosis have never defined him. From playing hockey to scoring field goals on the football team, find out how this athlete and Vikings fan is headed to the Super Bowl this weekend.

“I don’t think it would surprise anyone to learn that a lot of children love dogs,” says Emily DeBreto. “While we’ve had volunteers bring in therapeutic dogs at the hospital for comfort, we wanted to get our dogs more involved with the actual functional aspects of the therapy we’re providing.”

Elliot and his sister Amelia have a typical sibling relationship; they fight, they argue, they push each other’s buttons. But they have a unique relationship as well, that stems from Elliot's diagnosis with a rare chromosomal abnormality.

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.

Rebecca Pierce, the mother of a Gillette patient, speaks out about the importance of protecting Medicaid for children who have disabilities.

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.

“Using a wheelchair is good and bad at the same time. A disadvantage is you can’t run around outside like your friends. An advantage is you can cut the line at Nickelodeon Universe. Chair or not, I’m the same person.” See how care at Gillette has helped Elijah emerge as a leader.

Kelsey's attitude is so affecting, she says that most people don’t notice at first. Kelsey was born with a radial club hand, and her left arm is significantly shorter than her right. This means that when she’s instructing yoga—perhaps the most public of exercises—she’s essentially doing most of it, one-handed.

Katie Allee takes Advanced Placement classes. She’s 15, and she’s a straight-A student. Her mind? It’s all there, and she’ll tell you as much. But when it comes to her body physically, for much of her life, she’s had difficulty.

After a surprising scoliosis diagnosis, Avital Harris wore a back brace for two years. Now she is sharing her story, and plans for the future.

It’s delivery day. You’ve gone through all of the preparations for your newborn—from appointments and ultrasounds, to adding final touches on the nursery—and you are ready to finally meet your child. The last thing you hope for is any unexpected surprises.

Aaron Myers is like any other employee at The Works children’s museum with one exception: he is diagnosed with cerebral palsy. See how Aaron's family laid the groundwork for his successful transition to adulthood—and how the Gillette Transition Clinic is providing additional support.

Joe Carr is updating his Facebook status, taking photos with his iPad, teasing his older sister, and good-naturedly ignoring his mother’s pleas to get ready for his imminent floor hockey game. Meet this busy 13-year-old with an easy smile and a powerful laugh.

"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."

When 16-month-old Peyton ran across the living room, slipped, and hit his head on the hardwood floor, the impact left him fighting for his life. See how a partnership between Gillette and Regions Hospital helped Peyton achieve a full recovery, and why his parents consider Gillette part of their family.

Ava has a rare condition called multiple hereditary exostosis, which causes boney tumors to grow throughout her body. Learn what the condition means for Ava and why she looks forward to surgeries at Gillette.

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.

“They almost didn’t notice it at first,” Karey Hall says. When her daughter Katelyn was born, her left leg was missing two toes and had an abnormal, rainbow-like bend to it. “No one at the clinic had ever seen anything quite like it before.”

Mason and his father Rich saw nearly 500 rock bands live in concert last year. They refused to let Mason's cerebral palsy get in the way of reaching their goal.

84-year-old George Fedor is a storyteller. But the one story that George couldn’t tell had to do with one question: What is wrong with the left side of my body?

Joshua, a 10-year-old who has congenital scoliosis, dreamed of one day riding a bike. Learn about the groundbreaking surgery that straightened his severely curved spine, improving his independence and giving him the opportunity for a full childhood.

When Walker's parents and pediatrician became concerned about the shape of his head, their questions led to a diagnosis of craniosynostosis. Learn how a new surgical technique eliminated the need for a blood transfusion during Walker's craniosynostosis surgery.

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.