Children's Hospital Colorado

Children's Hospital Colorado

Hospitals and Health Care

Aurora, CO 64,684 followers

Here, it’s different.™

About us

Kids are incredibly different from adults, from their growing bodies to their developing minds. That’s why they need incredibly different care — the kind you’ll find at Children’s Hospital Colorado. As a nationally ranked pediatric hospital, we care for families throughout Colorado and surrounding states. Our comprehensive team of highly trained, experienced specialists cares for kids at all ages and stages of growth, through everyday ailments and extraordinary diagnoses. We see and treat more children than any hospital in the region, providing the expert care kids need to feel better, so they can get back to being kids. With more than 10,000 team members and faculty representing the full spectrum of pediatric specialties, our System of Care includes four pediatric hospitals, 10+ specialty care centers and 1,300+ outreach clinics. When you work at Children’s Colorado, you’re more than just a member of our multidisciplinary team. Here, you play a critical role in advancing our mission to improve child healthcare — a vision that has been at the center of our work since our founding. Children's Colorado has been reimagining child health for more than a century, and we’re just getting started. We're looking for talented, dedicated team members to carry that legacy forward. Start today — follow us! By using a Children's Colorado-branded social media channel, you agree to our Social Media Terms of Use: https://childrenscolorado.org/LinkedInTermsUse

Website
https://childrenscolorado.org/LinkedIn
Industry
Hospitals and Health Care
Company size
10,001+ employees
Headquarters
Aurora, CO
Type
Nonprofit
Founded
1897
Specialties
Pediatric Healthcare, pediatrics, pediatric specialty care, and healthcare

Locations

Employees at Children's Hospital Colorado

Updates

  • As a respiratory therapist, Meliza has seen firsthand the impact she can have on patients and families. Now, as a clinical manager and a leader in our Pediatric Respiratory Therapy Fellowship, she’s making an impact on our team members by helping fellow respiratory therapists gain the skills and training they need to feel confident caring for kids. For Meliza, moving from direct patient care to a leadership role has been a full-circle moment. And she wouldn’t want to do it anywhere else. “Here, it’s different. It’s fun. It’s engaging,” Meliza says. "And if at the end of the day, we did something right to help our patients get home and get better, that’s awesome.” If you’re a respiratory therapist who is passionate about working with kids, there’s a place for you at Children’s Colorado. Learn more about how we can help you transition to pediatric practice: https://lnkd.in/g-8D_JfG

  • Each year, Meg fractures between 15 and 20 bones. Not because she’s into exhilarating sports or dangerous hobbies, but because she has a genetic condition. Doctors diagnosed Meg before birth with osteogenesis imperfecta, also known as brittle bone disease, which makes her bones softer and easily fractured. During her pregnancy, doctors told Meg’s mom Leslie that Meg wouldn’t be born alive. But against all odds, Meg was born with nine broken bones and a fiery personality to take on the world. After a 12-day NICU stay, Meg established care with our experts and started bone infusions at 2 months old. Since then, she’s had 13 surgeries to put rods in her arms and legs that work as internal splints as she grows. “All of our friends have second homes in the mountains, and we have one in Aurora,” Leslie jokes. Meg’s bones are still very fragile, so she receives regular care from her pediatrician, one of our geneticists, Dr. Ellen Roy Elias, and other experts across our departments “Meg is an incredibly bright, talented and feisty 6th grader who has never let anything hold her back, despite her complex medical issues,” says Dr. Elias. “She is the perfect example of how impossible it is to predict the future in babies born with osteogenesis imperfecta. Her parents’ wish was for her to always attempt activities to allow her to have as normal a childhood as possible and to clearly make decisions supporting her happiness and quality of life.” And Meg is no stranger to our emergency department, especially since the smallest movement could result in a break. Last summer alone, Meg broke seven bones. But that didn’t stop her from participating in nearly every sport at her wheelchair sports camp. Regardless of her diagnosis, Meg doesn’t let anything hold her back. Now as a bustling sixth grader, Meg is a vocal major at Denver School of the Arts and once sang the national anthem at a Denver Nuggets game. This Wishbone Day, which raises awareness for osteogenesis imperfecta, Meg wants kids like her to know that your condition doesn’t limit your potential to shine. “Don't give up on what you want to do,” says Meg. “It may be hard, it may be scary, people may not believe in you, but you just can’t give up.”

    • Girl in a wheelchair holding a lacrosse stick
    • Girl laying in a hospital bed, leg in a cast, surrounded by stuffed animals
    • A girl in a wheel chair bike waving at the camera
    • A girl holding flowers in a wheel chair surrounded by a man, a woman and a boy
    • A girl in a wheelchair smiling with a boy holding flowers
  • Jonnie faced a lot early in his life — a heart murmur, multiple aneurysms and a heart condition that caused a hole in his heart. He had surgery to fix the hole in his heart, but optimal health still eluded him. “We didn’t understand why he was facing all these challenges,” says Drew, Jonnie’s dad. After a couple years of missing growth and health milestones, someone suggested genetic testing for Jonnie. Suddenly, everything made a lot more sense. Genetic testing revealed that Jonnie had multisystem smooth muscle dysfunction syndrome (MSMDS), an extremely rare disease that only about 50 people in the world have. Geneticists told Drew and Rachael that they should go see Dr. Kathyrn Chatfield at Children’s Hospital Colorado immediately. Dr. Chatfield is a genetic pediatric cardiologist and has treated all the cases of MSMDS that have come to Children’s Colorado. “It changed our life and it changed Jonnie’s life,” says Rachael, Jonnie’s mom. In working with Dr. Chatfield, who Rachael and Drew call, “The Queen,” they no longer guess about which care will help Jonnie. Now, they can proactively plan for his treatment — and the rest of his life.

  • Nearly 25% of Hispanic and Latinx families visiting Children’s Colorado say Spanish is their first language. SCORE fellows Shannon Acker, MD, and Jose Diaz-Miron, MD, are researching projects that could make it easier to share important health information with people who speak languages other than English. Learn how their work is improving health equity and outcomes for these populations: https://bit.ly/3TSFQdp

    • No alternative text description for this image
  • There's an increasing number of women who have become pregnant after being on weight loss drugs. Could there be a correlation? Dr. Melanie Cree, Director of the Polycystic Ovary Syndrome (PCOS) Clinic and national expert on PCOS research, shares her thoughts on why some physicians are turning to the drugs to treat PCOS, one of the leading causes of infertility in the U.S.

    Experts Call for More Data on Weight Loss Meds As Fertility Drugs

    Experts Call for More Data on Weight Loss Meds As Fertility Drugs

    beckershospitalreview.com

Similar pages

Browse jobs

Funding

Children's Hospital Colorado 3 total rounds

Last Round

Grant

US$ 300.0K

See more info on crunchbase