- Doctors & Departments
- Conditions & Advice
- Your Visit
- Research & Innovation
Watch the Miller family's interview about how the Colorado Fetal Care Center saved their twins' lives after a twin-to-twin transfusion syndrome (TTTS) diagnosis.
Watch Christine Kieft's interview about her son Cayden's spina bifida surgery at Colorado Fetal Care Center.
Learn about 19-year-old Alexa's experience with biliary atresia, and how our Pediatric Liver Center uses a multidisciplinary approach to provide the best care to her and other patients with the disease.
Learn about the difference Deep Brain Stimulation (DPS) is making for Dijmon Hill, who suffers from secondary dystonia.
Amara had biliary atresia, a progressive fibro-obliterative disorder affecting the liver and biliary system that results in end-stage liver disease and liver failure by age 2. Read her story to learn about her miracle and our hope for a better future for kids with biliary atresia.
“Career-ending” – that was Kiana’s initial diagnosis when her back spasmed so severely that her muscle protruded two inches from her left side. But, for this competitive swimmer, career-ending was not an option.
16-year-old Garrison Hayes was diagnosed with osteosarcoma, bone cancer, at 6 years old. Learn how he continues to race towards his dream of making it to the Paralympic Games.
After diagnosing 6-year-old Devan Ortiz with x-linked adrenoleukodystrophy (X-ALD), bone marrow transplant physician Dr. Ralph Quinones used genealogy to catch it in his cousin, Cole Chavez, helping to save Cole's life.
Sometimes injuries can be more severe than they first appear. Learn how high school athletic trainer Matt Brewer helped Cole Jones get the care he needed to recover from a severe shoulder injury that occurred during his wrestling match.
Truett Rosenlund has a rare, unknown, neuromuscular disease that has left him paralyzed from the neck down with nerve damage, and requires a tracheostomy with a ventilator and oxygen to breathe. Learn about his family's journey.
After her unborn baby was diagnosed with congenital diaphragmatic hernia, mom Lindsay came to the Colorado Fetal Care Center. Find out how she felt about her experience.
Read how the Colorado Fetal Care Center gave Noah a fighting chance in the midst of his Lymphangioma diagnosis. Our fetal care team of specialists gave hope to this family.
These twins, who first survived twin-to-twin transfusion syndrome (TTTS), continued to struggle before their birth. One of the twins was found to have congenital heart disease. After much difficulty, both girls are thriving.
After having two healthy babies survive twin twin transfusion syndrome, one mother wants to help others understand the condition through her journey.
Learn about a family's will to beat twin to twin transfusion syndrome & how the Colorado Fetal Care Center team created a treatment plan to help Joey & Paul.
JD's parents made a difficult choice when they opted for fetal surgery for their unborn son's myelomeningocele (spina bifida) to prevent hydrocephalus. Learn about their journey.
After a devastating diagnosis of Spina Bifida, one family turns to fetal surgery to help their unborn daughter, Emma.
Sam Baker was diagnosed with osteosarcoma, the most common type of bone cancer, before entering his senior year of high school. Learn how he partnered with his orthopedic surgeon, Dr. Travis Heare, to determine the right surgery for him.
Anneliese was born six weeks early with critical medical issues. She had respiratory failure and needed mechanical ventilation to support her breathing, as well as issues with her heart, hearing and vision. Read about her journey in our neonatal intensive care unit (NICU).
When Janelle and Mario Jackson learned their son Jaden had a congenital heart defect, there was a lot of uncertainty. Learn how they worked with our experts to ensure he received the best start toward a healthy life.