Paley Institute

More results...

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

Author name: admin

Brachymetatarsia, Patient Care

Jamie

After years of discomfort and pain for a birth defect, I was completely unaware of. I am eternally grateful for Dr. Lamm and the Paley Orthopedic Institute. Over the last three years, I had seen numerous specialists both within and outside of the USA and no one could give me answers to relieve my pain or any hope for a full recovery. Dr. Lamm and his team discovered internal issues and provided me with a vast amount of knowledge on the procedure and set realistic expectations on the entire recovery process. Dr. Lamm came highly recommended and qualified. His ability to quickly diagnose my condition after a set of X-rays was surreal. I was diagnosed with Brachymetatarsia with Tailor’s Bunion and Metatarsophalangeal arthritis. From the first time, Dr. Lamm walked into the room during my initial consultation I felt an immediate sense of relief as he displayed an exceptional bedside manner. I knew he was the man up for the task and with his assurance and confidence, I knew I was in the best hands possible. Eight months and two surgery’s later I am fully recovered and more pleased than ever! If I had to do it all over again I wouldn’t go through this process with ANYONE ELSE. What else can I say, Dr. Lamm is extremely knowledgeable in his field of expertise. He is a MIRACLE worker and has been gifted immensely in what he does. I will forever be indebted to him. THANK YOU DR. LAMM!!!

Patient Care, Scoliosis

Alexa

When my family found out that my daughter had scoliosis and would need surgery, we knew we were at a crossroads. We were concerned about finding the right doctor, about how Alexa‘s life would change following the surgery, and about even the risks of the surgery itself. We interviewed several doctors in the south Florida area, many of whom had impeccable credentials and were widely renowned. But when we finally had an appointment with Dr. Shufflebarger and his team, especially Miss Michelle, we knew we had found the right doctor for our daughter. Dr. Shufflebarger and his team put us right at ease and assured us that our baby girl was going to be just fine. In the months leading up to the surgery, they kept us informed about all aspects of what we needed to expect and what we needed to do for the surgery to be a complete success. In the days leading up to the surgery, they made sure that we were well taken care of and that Alexa would be in a great mental, emotional, and physical state for the surgery. Their facilities were absolutely perfect, and we did not have a single complaint. Alexa came out of the surgery a new little lady. While the first couple of weeks were a little bit painful, I can honestly say that she has not had any setbacks and came out of it perfect. We are now almost 2 years since the surgery, and I can’t remember a single time that she has complained of significant pain. We owe this blessing to Dr. Shufflebarger and his immense skill. We are so grateful that we chose him and his team, and to this day, we know we made the right choice. Alexa is now very interested in pursuing a medical career involving scoliosis, and she made such a connection with Dr. Shufflebarger’s staff that she is interested in doing an internship with his nurses. Dr. Shufflebarger made a huge impact in our lives, and we could not thank him enough. Thank you, Dr. Shufflebarger. Lester and Gabriella Hooker

Larsen Syndrome, Patient Care

Hannah

Our story began in July 2019 when we brought home the most beautiful, spunky, smart daughter who would just be turning eight years old! She was born with a rare “superpower” called Larsen Syndrome. She had undergone eight other surgeries in her country, without parents navigating things. Some of them, I am sure, were helpful and others not. It always matters WHO performs your surgeries, especially if you are a rare one like Hannah. Hannah could not stand up straight, she was in about a 90-degree bend. She did not have knees in the place where they usually are. Walking was a huge challenge. Before we left her home country, she asked her guide to translate this question to us, “Ask my parents if I will ever walk?” We arrived back in the States in late July 2019 and immediately began seeking medical advice concerning Hannah. Then the pandemic took the world by storm. We are self-employed jewelry makers who rely on trade shows to support our family of seven. We found ourselves in a financial situation, and the thoughts of helping Hannah anytime soon seemed to fade. It was October of 2020 when I felt God nudging me to take her back for another consultation with several doctors with opposing views. The situation that remained was that with major surgeries, Hannah could have straight legs and stand, but likely her knees would not BEND! That was not an option for us to gamble with. From that meeting, we decided that we would be seeking help from an expert at the Paley Orthopedic and Spine Institute, Dr. Feldman. The Paley Institute is a place with a lot of experience and specializes in more complex cases. I remember that Zoom meeting with Dr. Feldman in October and expressed my concerns about needing knees that bend. He said this, “Not bending is NOT an option! ” She will walk, and her knees will bend. God made the way financially during the pandemic despite our income problems through SO MANY giving people. We never even made a plea for help. It just poured in. In January, we loaded up and made our way to Florida. While her case was complicated, Dr. Feldman and Dr. Huser, with what we believe was God’s GREATEST favor and wisdom, performed miracles on her legs. We have only been home for about eight weeks, and we feel sure that Hannah has surpassed all expectations to date! We will edit our story soon to report more of her miraculous story as it unfolds. Hannah is enjoying the freedom of standing tall, walking with knees that bend. She is riding a bike, swimming, and loving her freedom! Thank you, Dr. Feldman, Dr. Huser, Monique, and the whole Paley team. Please don’t let the details of “the how” stop you from getting what you know your child needs. There are MANY ways to make it happen! The love and support at Paley is very evident! We are so glad to be a witness to all this greatness. We are forever grateful and thank God for his mercy and goodness!

Clubfoot, Patient Care

Griffen

Present at birth, clubfoot is one of the most common congenital deformities which occur in otherwise normal infants. Clubfoot is also known as congenital talipes equinovarus. Clubfoot affects 1 in 750 children worldwide. The cause of clubfoot is not known. One foot (unilateral) or both feet (bilateral) may be affected. Clubfoot can be seen at birth or sometimes during a prenatal ultrasound. The clubfoot turns down and inward. Clubfoot affects the tendons and ligaments not only in the foot but in the calf muscle as well. Clubfoot can range from mild to severe and will not resolve on its own. Clubfoot is not painful to babies. Though you might be worried, clubfoot treatment will help your child grow up to live a normal life. Nearly half of all cases (40%) occur bilaterally (affecting both feet). There appears to be a genetic component to clubfoot, as a 1965 study by Ruth Wynne-Davies reported that in families with one child born with clubfoot, the chance of a second child being born with the deformity is 1 in 35. Treatment for clubfoot is recommended at a very young age, often within a week or two of birth. At this age, progressive casting, known as the Ponseti Method, often results in complete correction with low rates of recurrence. A large number of cases, however, particularly those in developing countries, go untreated or are poorly treated. Individuals with untreated or poorly-treated clubfoot often suffer severely limited mobility and pain, resulting in staggering social, psychological, and financial consequences for not only the patient, but their family as well.

Arthrogryposis, Patient Care

Lucy

When Lucy was born she couldn’t move anything but her head. After being told by doctors in our area that they couldn’t start treatment on her legs until she was 18 months to 2 years old, we were determined to find another opinion. Thankfully we found Dr. Feldman and his therapy team. Lucy arrived at The Paley Institute when she was 4 months old. Her legs were stuck bent at the knees, she had clubbed feet, clubbed hands, and couldn’t bend her arms. She had serial casting, a tenotomy, serial splinting, and daily physical and occupational therapy. Her therapy included e-stim and astym. After her treatment, her legs were unstuck! We could put clothes with legs on her for the first time! She could kick her legs! She started moving her arms! And most recently Lucy stood for the first time by herself with the help of her HKAFO’s. We are forever grateful for The Paley Institute and can’t wait for Dr. Feldman to perform her leg surgery in the future to begin her journey of walking!

Patient Care, Tibial Hemimelia

Mitchell

I wanted to write you and thank you for the care you and your team gave our son, Mitchell. He had some “minor surgeries” over the years, but in 2011 you performed a femoral and tibial lengthening surgery on him. During that summer we moved to Jupiter so we could have all the physical therapy and follow up done there. Even as an experienced anesthesiologist, I was somewhat shocked at the amount of surgery and PT required to recover from this operation. As a Navy veteran, I never imagined that he could pass a military physical after all these leg operations so I believed the military was off the table as an option for him in life. In the intervening years, he was able to mountain climb with Boy Scouts in Philmont, New Mexico and hike the mountains in Montana elk hunting with me as well as become a very good scuba diver. However, in 2019 we saw you for a clearance evaluation as my son wanted to apply to the U.S. Merchant Marine academy which requires a Congressional Nomination and to pass the standard military physical. Thanks to you and your team’s effort, he was able to pass his physical and subsequently was granted an appointment to the Academy. He has now finished his first year and is on his first deployment on a cargo ship for three months. I know the last year has been very difficult for everyone so I wanted to update you on one of your success stories. Even though you haven’t heard from us lately, we remain grateful you were able to help our son.

Patient Care, Tibial Hemimelia

Kevin

Kevin was born on December 5, 2017 in Turin italy with a malformation in his right leg. The whole thing had not been diagnosed during pregnancy and was only discovered at birth. The pathology is called TIBIAL HEMIMELIA, Kevin was born without the patella and without the tibia and his leg is 4cm shorter and bent inwards. In addition, he has a bifurcation of the femur to make the leg even more complex. Given the rarity of this malformation, unfortunately it is still little known and no one in Italy performs this treatment, after 7 unsuccessful interventions. The only solution that was proposed to us was amputation. Not only in Italy but throughout Europe. It is a very rare disease with an incidence of one in a million. Kevin is that baby in a million. To be able to walk, Kevin needs a series of delicate interventions that only dr. Paley can perform successfully. La STORIA di Kevin Kevin è nato il 5 dicembre 2017 a Torino con una malformazione alla gamba destra. Il tutto non era stato diagnosticato in gravidanza ed è stato scoperto solo alla nascita. La patologia si chiama EMIMELIA TIBIALE , Kevin è nato senza la rotula e senza tibia è la gamba di lui è 4cm più corta e piegata verso l’ interno. In più lui ha una biforcazione del femore a rendere la gamba ancora più complessa. Data la rarità di questa malformazione purtroppo è ancora poco conosciuta e nessuno in Italia esegue questo trattamento, dopo 7 interventi non riusciti L’unica soluzione che ci è stata proposta è stata l’amputazione. Non solo in Italia ma in tutto Europa. È una patologia rarissima con un’incidenza di uno su un milione. Kevin è quel bambino su un milione. Per poter camminare kevin ha bisogno di una serie di delicati interventi che solo dott. Paley può eseguire con successo.

Congenital Femoral Deficiency, Patient Care

Everly

Everly was born with Fibular Hemimelia and Congenital Femoral Deficiency in her left leg — she had lacked ankle structure, had a dislocated hip (not born with it), and did not have a fibula. After seeing multiple specialists in the United States we finally met with Dr. Paley and his team when Everly was 6-months old. We were advised to attend Children’s Mercy in Kansas City, Ks for roughly 6-months to attempt fixing her dislocated hip without having surgery, albeit with no success. At that point, Dr. Paley confidently and calmly put us to ease with a concrete gameplan: Everly would need SUPERhip and SUPERankle surgeries before any lengthening could begin. Then Covid-19 hit. While the world was seemingly turning upside-down, Dr. Paley assured us that nothing would change with Everly’s first corrective surgeries (SUPERhip and SUPERankle) in April of 2020 as she was only 18-months old. Both surgeries went according to plan and Everly was up and running, literally, once she came out of her spica cast. The next step in the process was Everly’s first limb-lengthening in April of 2021 at the age of two. Everly qualified for the internal device that would lengthen her femur. Dr. Paley and Dr. Shannon were incredible. Dr. Shannon would regularly and promptly answer emails with any questions we as a family had following surgery. As of now, the medical team believes that she will most likely need 2-3 more limb-lengthening surgeries. Following this surgery we got to experience the full Paley Experience — and that is the “family” that is the Physical Therapy team. Daily PT seemed daunting, but Everly looked forward to seeing her therapists and friends she met at PT. We as a family equally looked forward to seeing these familiar faces and smiles and we were able to make lifelong friends. Dr. Paley, Dr. Shannon, and the entire PT team at the Paley Institute have given our daughter the chance to excel in life. We still have many more years in this journey, but we are 100% confident the Paley Institute is the #1 place in the world for our daughter’s needs. Tyler and Shauna, proud parents of Everly

Knee Surgery, Patient Care

Barbara

Dear Dr. Paley, I had originally seen Dr. Minus as I was having problems with my right knee. He ordered an MRI and discovered that I had a torn meniscus. Dr. Minus recommended physical therapy to see if that would correct my problem. Sadly, the blood supply is limited in that area and it did not heal. Now, Dr. Minus was away for 3 weeks and I really needed to get this problem resolved ASAP. Since I am close friends with Allison Lamm, Allison was so helpful, arranging for me to see Dr. McVicker for knee surgery on my meniscus. My husband and I met with Dr. McVicker and he was available the following week so we signed up to proceed. I am writing to you to tell you how amazing the whole process proceeded. I was operated on at the surgical center adjacent to Palm Beach Orthopedic center. My husband and I were so impressed with Dr. Mcvicker’s team. Lisa, his secretary is by far, the most gracious and efficient assistant. She was always so helpful and never kept me waiting if I had any issues or questions. When Dr. McVicker was unavaiable, his assistant, Liam was there as a great back up and he took care of any inquiries that needed answers. At one point, I called Lisa to find out if I would be able to do Cryo Therapy. She returned my call promptly and told me that Dr. McVicker said it was okay to do Cryo. I am so glad I did as it took away so much of the inflammation, I was able to walk with a more flexible knee and the pain had subsided a great deal. That was at the two week mark and the rest of the recovery was easy. I was able to swim since the stitches had healed and also I was able to ride my bike. At my 8th week check up, I was told I could proceed with my tennis. I started out with hitting the balls on a ball machine with Allison, then I took several lessons, played 2 social games and then played a match for the team that I Captain. That match lasted 2 1/2 hours and I felt okay after the match. I did ice and now I am playing 3 times a week. I am very pleased with the Paley group, you have an amazing team. The work that is performed within your practice is totally amazing, limb lengthening, club feet reconstructed etc. Kudos to you and your team. I will recommend your group to anyone that needs the best of care. Sincerely, Barbara

Dr. Paley talks paley institute and patient fun run
Latest News

Exclusive Interview with Dr. Paley on Patient Care, Innovation, and the Upcoming Patient Fun Run

Dr. Paley discusses the innovative approach of the Paley Institute and its involvement in the Palm Beaches Marathon, with a special emphasis on supporting the upcoming Patient Fun Run. This event provides an opportunity to celebrate the resilience and achievements of our patients, including inspiring stories like that of Tommi Rice, while promoting community engagement and raising awareness. WATCH FULL INTERVIEW