Paley Institute

More results...

Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
page

Paul

Paul is the cutest, best kid ever. He’s funny. He’s smart. He’s got great dance moves. Every one loves him and he is known as the mayor wherever he goes. He’s a great kid. So all greatness aside, he was also born with a host of medical issues. Upon delivery, the nursing staff noticed that he had a right clubfoot. So, that’s when the speculating began. “He has Downs Syndrome.” (He doesn’t.) “He might have Noonan Syndrome.” (He doesn’t.) Etc. All we saw was a cute, peaceful little blond boy with a cute crooked little right foot. So, our initiation into parenthood was not your typical experience. But we were up for the challenge. To make a long story short, Paul’s symptoms are: a right clubfoot, left ptosis (droopy eyelid), camptodactyly (contractures of his fingers), left torticollis (his head tilts to the left), his legs don’t fully straighten and, most seriously, congenital scoliosis. His overarching diagnosis is arthrogryposis.

We first brought him to Dr. Feldman when he was about 3 months old seeking a second opinion, because the pediatric orthopedist who was treating his clubfoot was not being forthcoming about whether or not he was truly using the Ponsetti method, which we knew to be the golden standard of clubfoot treatment. After meeting with Dr. Feldman, we knew we had to switch over and continue Paul’s treatment with him. Aside from his confidence, credentials, experience, etc.—he was also the first and only doctor to ever say: “If this was my child, this is what I would do.” He saw Paul as a person from the beginning. When we discovered that Paul also had spinal abnormalities at around 8 months of age, we knew that it was fate or some sort of divine intervention that had brought us to Dr. Feldman earlier that year. And now, 9 years later, and quite a few surgeries later—some of which are ongoing, such as the bi-annual VEPTR adjustments—Paul is still a happy, energetic, smart, social kid. He runs, dances, sings, jumps, reads, hugs, etc. Pretty typical kid stuff. Except he’s had to deal with more than some other kids. He plans on being a chef, inventor or U.S. President someday, and we believe that he can accomplish anything he puts his mind to—and for that hope, we will always be grateful to Dr. Feldman for guiding us on our curved journey.

Tony & Kelly

More Patient Stories

Mosope
Mosope

On 31st December 2010, we received our new year gift with the birth of Mosope, amid the celebration, there was a challenge, Mosope was born with Proximal focal femoral deficiency (PFFD), i got confused as i have never seen nor hear of this condition. We immediately met with our local doctor that referred us to an orthopaedic consultant, the Professor

Read More
Larry

When a person is diagnosed with a serious medical condition that requires surgery, usually they seek a second opinion that hopefully informs them that things are not so dire. Imagine when the second physician tells the patient that not only is surgery required, but an additional procedure is needed as well. This is what happened to me. Upon a neurologist’s

Read More
The boy you see in the photo with Dr. Paley is my son Giovanni, who suffers from tibial pseudoarthrosis.
Giovanni

The man of miracles. Who is Dr. Paley? Dr. Paley (for the few who still don’t know) is a world-renowned orthopedic surgeon, often called “the bone wizard,” known for his pioneering work in limb lengthening and deformity correction. He has invented or perfected about 100 surgical procedures related to limb reconstruction and deformity correction, and his protocols are used and

Read More