Paley Institute

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Our little girl was diagnosed with Proximal Femoral Focal Deficiency when she was born. We saw Dr. Paley when she was nine months old and he put our fears to rest!

He immediately had a game plan in place and assured us he could help our daughter. She had a hip and knee surgery with him when she was two and her first limb lengthening surgery when she was three.

Thanks to Dr. Paley and his team, she now has two even legs for the first time in her life! I cannot say enough about Dr. Paley! He is an amazing man and is an expert in his field.

I would entrust my daughter to his care at any moment and would without reservation recommend him as well. We are very grateful for the difference he has made in our daughter’s life!

Lillie is now almost 10 and we are currently going through her second limb lengthening with Dr. Paley. We have the internal device this time around and so far things are going very well. Ten years later, we still wholeheartedly stand behind our support and endorsement of Dr. Paley and his team. You will not find a man more knowledgeable and capable in this specialized field. We will forever be indebted to him.

Chrystal
Augusta, GA

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Justin Faced Amputation After 6 Failed Surgeries — Dr. Dror Paley Saved His Leg
Justin

At just 11 years old, Justin had already endured six failed surgeries and lived with the constant fear of breaking his leg again. Born with congenital pseudarthrosis of the tibia (CPT), a rare and challenging bone condition often linked to neurofibromatosis type 1 (NF1), Justin faced a future of limitations—and the looming possibility of amputation. But everything changed when he

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Lorenzo

Mi chiamo Anna e sono di Napoli,Italia. Ho un bambino di 7 anni di nome Lorenzo.Mio figlio è nato con la pseudoartrosi congenita di tibia.Ha avuto 11 interventi in Italia!!durante uno dei quali,ha contratto un’infezione da stafiloococco aureo,evolutasi poi in una osteomelite cronica!Avevo perso ogni speranza che mio figlio potesse guarire da questa pseudoartrosi infetta..in talia infatti,gli erano stati somministrati

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Noah - Fibular Hemimelia
Noah

Our son Noah was born with Fibular Hemimelia and we noticed it immediately because he had a smaller foot and missing toe. We live in Houston TX and soon discovered that most Pediatric Ortho doctors have minimal to no experience treating this condition. We bounced around a bit and ended up at the best facility in Texas. We were following

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