Share Your Story: I Got This

Share Your Story: I Got This

Meet Ella, a patient who is treated by our experts in the Center for Excellence in Clubfoot and Foot Disorders. Learn more about her journey below. Blog written by Ella’s mother, Lindsay.  I was about halfway through my pregnancy when we found out that our baby, Ella, would be born with a clubfoot. Our standard anatomy scan revealed we were going to have a baby girl, plus indicated there might additional issues going on.  

Our doctor referred us to a specialist, where we learned that Ella most likely had a rare heart condition called Tetralogy of Fallot, in addition to clubfoot. In order to confirm the heart condition, her little heart needed more time to grow and develop. That waiting period was very stressful, but after a couple of weeks and many prayers, we learned that Ella had a healthy heart. She still had clubfoot, so we then went to a different specialist in Oklahoma City.     As soon as she was born, we started her clubfoot treatment. I wanted to be on top of things and give her the very best possible outcome. Immediately following her birth, Ella’s left foot was casted for four weeks. She then had an Achilles tenotomy procedure, where the Achilles tendon was cut so the ankle

During this time, I remember feeling a lot of guilt because our doctor would tell my husband and me that we needed to be doing more. More stretching and more exercises with Ella. My mom intuition kicked in, and I had a bad gut feeling that something just wasn’t right. Her little foot literally wouldn’t stretch anymore, so I consulted with a physical therapist who confirmed my feelings.     Ella underwent another Achilles tenotomy in January of 2019, followed by a tibial osteotomy in December of 2019. During the tibial osteotomy, her tibia was cut and repositioned. This caused Ella to be in extreme pain. We did not have a very good experience at that original hospital, and that was when that I started to research other hospitals and learned about Scottish Rite for Children.  

I reached out to a respected doctor that I know, and he referred us to Scottish Rite. He told us that the doctors at Scottish Rite were the absolute best! And they are! Ella’s first appointment with Dr. Riccio was in the fall of 2020. At that time, he told us what we didn’t want to hear – another surgery would be necessary for Ella. We had been through so much with our first doctor and hospital that I was very uncertain and had lots of anxiety about what to do.    After much prayer, we decided to schedule a tendon transfer and release surgery with Dr. Riccio.

He could sense that I was afraid, and I was so touched with how he took the time to talk to us and help ease my fears.

The day of her surgery, I was a complete mess. I had stayed up all night, going down a dark rabbit hole on the internet. I will never forget when Dr. Riccio walked in the pre-op area and said, “I got this”. After her surgery, he came to talk with us in recovery and had a huge smile on his face as he walked into the room. He told us that he thought we were going to be very happy with the results. Those memories will be in my mind forever. We are thrilled with the results! We are FOREVER thankful to Dr. Riccio and his entire team. The kindness Ella experienced with the Child Life team was also life changing. Our entire family thanks God for Dr. Riccio and I tell anyone who has a child with clubfoot to go to see him immediately!  

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What are Flat Feet?

What are Flat Feet?

At Scottish Rite for Children, the Center for Excellence in Foot includes a multidisciplinary team of experts who collaborate to determine the best treatment plan for each patient. We know there are a lot of questions if your child begins treatment for their flat feet (Pes Planus). Below are the most commonly asked and the answers from our team. What are flat feet? Flat feet are the flattening of the arches of the feet when standing. What is the cause? Children’s bones and joints are flexible, which can cause their feet to flatten when they stand. Babies are often born with flat feet, and this condition may continue into early childhood. Flat feet can also be hereditary or run-in families. In most children, the feet become less flexible, the arch develops, and flat feet disappear by the age of five or six, but some children continue to have flat feet into adulthood. Do flat feet cause pain? Flat feet are usually painless and do not interfere with walking or participation in sports. In young children, flat feet are not associated with pain to the knees, hips or back. What are the two types of flat feet? 1. Flexible flat feet
  • A flexible flat foot is a variation of a normal foot.
  • Flexible flat feet can be normal in most infants and toddlers, as the arch has not yet developed.
  • The arch is visible when the child is sitting or on their tiptoes, but the arch collapses when the child is standing.
  • This type may be seen in multiple family members.
2. Rigid flat feet
  • A rigid flat foot means that there is no arch in the foot, even when the child is standing on the tiptoes.
  • The motion of the foot and ankle is stiff.
  • X-rays or other imaging may be ordered to determine why your child has a rigid flat foot.
What are treatments for painful flat feet?
  • Most flat feet are not painful and do not require any treatment.
  • For painful flat feet, treatment is focused on comfort and flexibility.
    • Shoe inserts or tennis shoes with a stiff sole and good arch support may be used for painful flat feet, but they will not permanently change the appearance of the foot.
    • Over-the-counter gel and soft shoe inserts are often recommended.
    •  Hard plastic inserts tend to cause discomfort.
    • A referral may be made to an orthotist, for custom shoe inserts.
  • A stretching exercise program may be recommended for flexible flat feet with tight heel cords.
  • Surgery is not recommended in most cases of flat feet.
Learn more about the common foot disorders our experts treat.
Share Your Story: Wide Open Future

Share Your Story: Wide Open Future

Meet Larry, a patient who is treated by our experts in the Center for Excellence in Foot. Learn more about his journey below.

Blog written by Larry.

My name is Larry, and I was born with bilateral clubfeet. After years of treatment at other hospitals, my family found Scottish Rite for Children when I was 5, and ever since then, it has changed my life. At the age of 15, I had my reconstruction/leg lengthening of my left foot, which was more severe than my right. The way my left foot was formed, I was always walking in a tiptoe position, without any ankle movement. And then on my right side, I wore a brace and needed a shoelift to help balance things out. Dr. Riccio and his team did a miracle on me, the impossible reconstruction of my foot and ankle along with lengthening my left leg with a fixator.

Throughout my time at Scottish Rite, I participated in research studies so I could help the doctors learn more about clubfoot and allow other people to benefit from their findings. I believe that more has to be done, and I want to do my part in helping out.

RUNGE 75 75 OSTRIS. A football player with the number 75 on his jersey

Although I faced many challenges with my condition, it has never stopped me from participating in everything I love.

I grew up playing Little League baseball, worked at my local CrossFit gym, participated in track and field and also played varsity high school football. Today, I am enjoying my senior year in high school, and I am in my final season on the varsity baseball team playing first base. After graduation, I hope to attend college to earn my associate degree in business and then attend the Universal Technical Institute in Houston, Texas for diesel/automotive mechanical school. 

My future is wide open, and I continue to go beyond my own expectations. I want to thank Scottish Rite, Dr. Riccio and his team along with all the staff for providing the best care to me. Because of Scottish Rite, I am able to walk and run with both of my feet!

 of Larry’s clubfoot journey.

 

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Juvenile Bunion Deformities

Juvenile Bunion Deformities

This article was recently published in the Pediatric Society of Greater Dallas newsletter. Committed to improving orthopedics care of pediatric patients in all settings, Scottish Rite for Children specialists are regular contributors to this publication for local pediatricians.

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What are Juvenile Bunions?
Juvenile bunions, a deformity of the foot, are a common cause of frustration for patients, their parents and medical providers. Fortunately, the vast majority of bunion deformities in children and adolescents are asymptomatic and therefore require no intervention aside from parental reassurance. For those deformities that cause difficulty with shoe wear and pain refractory to conservative treatment modalities, surgical correction is a reasonable option. It cannot be overstated, however, that appropriate surgical management mandates an in-depth understanding of the component deformities to avoid the historically high rate of recurrence and failure following operative treatment.

How Do Adult Juvenile Bunions Differ From Adult Bunions?
Clinically, adult and juvenile bunions appear very similar with lateral deviation of the great toe and a medial eminence at the metatarsophalangeal (MTP) joint resulting from uncoverage of the medial metatarsal head. These are, however, very different deformities. Adult bunions are
most commonly acquired deformities from tight shoe wear which leads to attenuation of the medial sided soft tissues at the MTP joint, lateral deviation of the hallux and usually pronation of the toe as well.

What Causes Bunions?
The cause of juvenile bunions is neither completely understood nor agreed upon. Hypermobility of the first ray, an associated flatfoot and obliquity of the lateral cuneiform have all been postulated as causative factors. However, the deformity is most likely congenital and results from external orientation of the articular surface of the metatarsal head.

How Do Bunions Appear in Radiographs?

Radiographically, both adult and juvenile bunions are characterized by angulation between the first metatarsal and the proximal phalanx (hallux valgus angle or HVA) as well as an increase in the angle subtended by the axes of the first and second metatarsals (intermetatarsal angle or IMA). The distinguishing characteristic of the juvenile deformity is a more lateral orientation of the distal metatarsal articular surface. Whereas in adult bunions, the articular surface is usually perpendicular to the metatarsal shaft. In younger patients, the angle between the shaft and the articular surface (distal metatarsal articular angle or DMAA) is elevated. This results in lateral deviation of the toe with maintained congruency of the MTP joint. In contrast, adult bunions usually demonstrate varying degrees of joint incongruency between the base of the proximal phalanx and the metatarsal head.

Can Bunions Be Prevented?
Because juvenile bunions are congenitally acquired, there are no means by which the deformity can be prevented. Moreover, once noticed, no well-accepted means of stopping deformity progression are available. Commercially available toe spacers, bunion straps and physical therapy cannot alter the abnormal anatomy of the distal metatarsal articular surface and therefore have no role in the management of this clinical entity. Straps and spacers that force the great toe more medially and the give the outward appearance of a straighter hallux do so by creating incongruity at the MTP joint which can alter range of motion and oftentimes cause discomfort.

What Shoes and Pads Help with Juvenile Bunions?
As mentioned above, in the absence of pain or difficulty with shoe wear, parental reassurance is the best course of action. In the presence of symptomatic deformities, nonoperative measures are all that is usually required to keep children active and happy. Shoe wear modifications are the simplest and oftentimes most effective course of action. Adolescents and their parents should be encouraged to find a well cushioned stability shoe with a wide toe box and flexible uppers. For those children required to wear leather shoes, boots or cleats due to school uniform requirements or recreational desires, most cobblers can create extra space in the region of the medial eminence using a “ball and ring” shoe stretcher. Should shoe modifications fail to provide complete relief, silicone bunion pads placed over the medial eminence can also be helpful. In children with flexible flatfoot deformities and symptomatic bunions, using a soft shoe insert to elevate the medial half of the heel and support the arch can offload any plantar-medial pressure by elevating the medial column of the foot.

Is Surgery Necessary for Bunions?
When prolonged conservative treatments fail to provide relief, surgical intervention is a reasonable option. Though recommendations vary with regard to the timing of surgery, due to historically poor results following the surgical treatment of juvenile bunions, many advocate to delay surgery until adolescents are within one or two years of skeletal maturity.

Females typically reach skeletal maturity at age 14 while males reach skeletal maturity at age 16. Better understanding of the congenital nature of the juvenile bunion and the importance of correcting the DMAA during operative treatment will likely lead to a dramatic reduction in recurrence and surgical failure, ultimately driving down the age at which operative intervention can be successfully undertaken.

Who is Qualified to Perform Surgery to Correct Juvenile Bunions?
As such, surgery should be performed only by those with a clear understanding of this specific deformity such as a fellowship-trained pediatric orthopedic surgeon or a fellowship-trained orthopedic foot and ankle specialist who is comfortable caring for pediatric patients.

Anthony I. Riccio, M.D., is a pediatric orthopedic surgeon caring for children and adolescents at Scottish Rite for Children. He is the director for the Center for Excellence for Foot.

Share Your Story: A Visit From the Tooth Fairy

Share Your Story: A Visit From the Tooth Fairy

Meet Jade, a patient who is treated by our experts in the Center for Excellence in Foot. Learn more about her journey below.

Blog written by Jade’s mom, Deirdra, of South Carolina. 

We first noticed a growth on Jade’s ankle in March 2017. Initially, we went to her pediatrician and were told that it was cancer. They did an X-ray and the doctor could not determine what the growth was. He then sent us to Scottish Rite for Children and as soon as we met with Dr. McIntosh we all felt better

Jade needed a CT scan to take a better look at her ankle. Luckily, we learned that she in fact did NOT have cancer. Jade has an incredibly rare condition called Trevor’s Disease. Basically, this causes an overgrowth of cartilage and we were told to come back in six months to check for additional growth.

In October 2017, Jade started to experience pain when walking and running. It also happened to be time for her follow-up appointment, so after discussion with Dr. McIntosh, we determined that surgery would be the best option for Jade. Her surgery was scheduled for the next month. It was the day of her surgery and everyone was amazing – the nursing staff, the doctors and even the pastor who prayed with us made us feel at ease. Jade did wonderful and even woke up a few dollars richer. She had a couple of loose teeth that the anesthesiologist needed to remove, and the tooth fairy visited her in the operating room! It was incredibly special for us to have such a caring staff.

At the time of her surgery, we were living in Texas. We have since moved to South Carolina, but we still make annual trips back to Dallas just to see Dr. McIntosh for Jade’s follow-up appointments. Scottish Rite for Children means everything to us. Everyone is willing to help, and they make all children feel special. When a kiddo is going through major surgery, it is so nice to have amazing staff surround you for every step of the journey.

DO YOU HAVE A STORY? WE WANT TO HEAR IT! SHARE YOUR STORY WITH US.

Get to Know our SRH Staff: Carrie Wilson, Ambulatory Care

Get to Know our SRH Staff: Carrie Wilson, Ambulatory Care

What is your role at the hospital? 

I am the RN coordinator for Dr. Richards and I also assist with Dr. Sucato’s scoliosis clinic. My primary role is providing education to patients and families, as well as helping to get patients ready for surgery to make sure medical clearances are obtained. One day to the next is never the same!

What do you enjoy most about Scottish Rite for Children?
The patients and their families!

What was your first job? What path did you take to get here? How long have you worked here?
My very first job was as a lifeguard when I was in high school. During college, I had several different jobs. I worked at a restaurant in the summers (where I met my husband to be), I worked for a stockbroker and I worked at Dillard’s.

I started at the hospital during my last semester at Texas Woman’s University. I was initially a nurse tech and then after I graduated, I was hired as a full-time inpatient nurse. As of this month, I have worked here for 32 years and I’ve been the RN coordinator for Dr. Richards for the past 22 years.

What are you currently watching on Netflix?

Call the Midwife
Who would you most like to swap places with for a day?

Jerry Jones (owner of the Dallas Cowboys) – although I don’t think he could handle my job if we had to “swap”!
What is a fun or interesting fact about your hometown?My hometown is Des Plaines, Illinois. It is the home of the first McDonald’s franchise.
What is your favorite thing to do when you’re not working?
Watching football and spending time with my family.