On April 11, 2016, I delivered my first child, a baby girl, named Claire. When I was admitted to the hospital, my doctor discovered that my daughter was breech presentation. The decision to pursue a caesarean section was made.

Immediately post-op everything was a blur. I was exhausted and barely able to stay awake. The next morning, the pediatrician came to visit and on his examination, he determined her left hip had a “click” which was concerning for hip dysplasia.

As a new parent, I was nervous to hear that my otherwise, healthy, full-term baby might have a problem with her hip development. As a nurse practitioner, my mind immediately thought about possible long-term complications (delayed or impaired ability to walk, etc.) However, since I work in critical care, I tried to put the information into perspective. I told myself, I just had a healthy baby and a successful surgery and that I needed to worry less and trust more. The pediatrician was wonderful! He referred us to the pediatric orthopedist. The orthopedist recommended a Pavlik harness, a type of fabric stabilizing device, to help keep the hip in the correct position and allow the joint to further develop. I did not realize that an infant’s hips are rather malleable and so by diagnosing Claire’s hip dysplasia early, the harness could reposition her hip and allow for healing over the course of several weeks. She wore the harness for about 12 weeks and had some follow-up ultrasounds and then x-rays to confirm resolution.

At the time, the harness made taking care of a newborn a little more complicated, especially with diaper changes because there were a lot of straps to re-secure. Now, my daughter is 21 months, and I barely remember the Pavlik harness. She is not only walking but running with no pain and no physical limitations.

My gratitude for her pediatrician who astutely and promptly diagnosed her hip dysplasia and for the expertise of her pediatric orthopedist will endure for the rest of my life. They took wonderful care of my daughter! Since Claire’s experience, I had another friend whose daughter was breech and had hip dysplasia. It was so nice to be able to share my experience and encourage her and her husband as they went through a very similar situation. My hope is this post will also encourage you! Please share your experience with family, friends, neighbors, etc. to help raise awareness of a problem, that if detected early, can be be successfully treated as if it never existed in the first place.

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  1. Mary Hassett says:

    I was born in 1953 with CDH as it was called back then ! Unfortunately it went undetected until I was 18 months old …. and so began years of surgeries and disability. Both my children were born with hipdysplasia and also one granddaughter all had early detection this is vital to save years of heartache…. so pleased this condition has been brought to light .

  2. Penelope says:

    I also was born in 1953. I am now facing total hip replacement. I was never screened. I have always been athletic, but always just had one problem or another. I am very discouraged that it was not diagnosed as an infant.

  3. Hailey Raskin says:

    My daughter, born in 2009, was diagnosed with hip dysplasia at 6mos and required a Spica cast followed by the pavilion harness. It is with a grateful heart that I tell you she is completely unaffected now. Her name is Claire.

  4. Cassandra says:

    Thank you so much for your story! I have just had a newborn boy and although he was not breech he had hip instability that warrented the harness. Being that he is our first child we have been very stressed dealing with this and adjusting to being new parents. Your story encourages us to remain positive while we work through this together. Thank you again and God bless.

  5. Amy Lafferty says:

    I have a 5 year old daughter that was diagnosed with hip Dysplasia. She was in a pavlik harness for about 4 weeks, and then in another brace until she was 2. When she was two the x-rays were showing things were looking great, and she just needed a check up when she is 4. When she turned 4, the hip socket was showing it wasn’t covering the ball all the way, now at her 5 year check up it has gotten worse, and now want her to do salter ostemoy surgery. This is my first daughter and i want her healthy, but the idea of her going through surgery has me scared for multiple reasons. IF anyone has gone through this surgery, comforting words of wisdom would be greatly appreciated. Thank you.

  6. Linneka Caruth says:

    thank you so much for your story and the success that came with it!! your story encourages parents who have a child will the same diagnosis to remain positive while they work through the process.

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