Boston Othotics and Prosthetics

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.

Truth vs Myth: Expert Answers to Common Parent Questions About Plagiocephaly

Truth vs Myth: Expert Answers to Common Parent Questions About Plagiocephaly

Plagiocephaly, or “flat-head syndrome,” is a relatively common condition characterized by a flat spot on the back or side of a baby’s head. Plagiocephaly can be caused when the baby’s head frequently rests in the same position on everyday surfaces such as a mattress or car seat, or it can even happen in the womb. It can develop in as little as one week and is present to some degree in nearly half of infants.

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Fixing Bennett’s Flat-Head Syndrome

Fixing Bennett’s Flat-Head Syndrome

Shortly after Bennett Hirsh was born she was diagnosed with plagiocephaly — flat head syndrome — commonly associated with torticollis. Babies with torticollis have a hard time turning their heads because of their tight neck muscles. When they lie down, they tend to keep their heads in the same position. Since the bones of the skull are soft and have not fused yet, this can cause flattening.

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Q&A with Shawn Koehler, CPO, Boston O&P

Q&A with Shawn Koehler, CPO, Boston O&P

Shawn Koehler is a certified orthotist who specializes in lower limb orthortics at the Boston O&P clinics in Annapolis and Lanham, Maryland. In this Q&A, Shawn shares how he was introduced to the field of orthotics, how Boston O&P’s lower limb orthotics differ from those offered by other companies, and his goals for his career.

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My Courageous Carter

My Courageous Carter

To say the words “cerebral palsy” in regards to my child was very difficult. For a long time, since my son Carter's diagnosis in 2016, I was not prepared to tell people my son had CP. Maybe it's because I was afraid of people judging him or not giving him enough of a chance. I wanted so badly to make sure he had the opportunity to fight all of his obstacles.

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by Natalie Avellone  | 

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