Catherine Falcone is a certified orthotist/prosthetist who specializes in Pediatric Orthotics and Prosthetics and Adolescent Idiopathic Scoliosis (AIS) at the Boston O&P clinic in St. Louis, Missouri. In this Q&A, Catherine shares how she was introduced to the field of pediatric orthotics and her personal philosophy on patient care.
The Bill Miller Blog
Named after Bill Miller, the founder and inventor of the Boston Brace, who had two great passions in his life – innovation and compassionate care for patients.
By reading these blog posts you will learn more about conditions including scoliosis, plagiocephaly, and lower limb and neuromuscular conditions, including technological advancements, treatment options, and how Boston Orthotics & Prosthetics is working to improve the lives of the people we serve. Bill's spirit lives on here.
Twelve-year-old brothers, Caden and Ryan Kim, share many similar characteristics and common interests — they both love to ski, read, build models out of wood and cardboard, and both play the violin. But one thing these identical twins don’t share is a condition known as idiopathic scoliosis, a curvature of the spine with no known cause.
If you have been researching bracing as a treatment for scoliosis, you’ve probably come across the terms “custom bracing,” “custom fabricated,” or “custom fitting.” So, what do these terms mean?
Fifteen-year-old Eli is by most accounts a typical teenage boy. He is active on his high-school wrestling team, a Boy Scout, and also enjoys snow skiing and water skiing. However, Eli is far from typical.
If you’re reading this, you or a child you know has probably been diagnosed with scoliosis, and your doctor has recommended bracing as an effective course of treatment.
Although tiny for her age, two-year-old Aggie is “fierce and full of life,” says her mom — much like Agnes Gru, the character in the movie, Despicable Me, who inspired her name.
Kate is by all accounts ahead of the learning curve. “She's an extremely smart little kid,” says her Dad, Patrick Brown. “She's known all the letters of the alphabet since she was two and a half.”
Like many couples, Kerry Adams and her husband, Derek, eagerly began preparing for the arrival of their first child. What they didn’t prepare for was the unexpected news that their son had myelomeningocele, one of the most severe forms of spina bifida, in which the spinal cord fails to close during development.