When Clinical Care Feels Like Family, De’Vaun Rediscovers His Stride

When Clinical Care Feels Like Family, De’Vaun Rediscovers His Stride

Previously published in Rite Up, 2025 – Issue 3

Family means everything to 6-year-old De’Vaun, of Forney, Texas. Most of De’Vaun’s favorite activities, like watching movies or playing with Legos, are enjoyed best with his parents and older sisters. What he did not know is that his family would grow because his care team at Scottish Rite for Children would become an extension of home.

When De’Vaun’s parents noticed his left leg had bumps on the skin and was curving inward, they came to Scottish Rite’s Center for Excellence in Limb Lengthening and Reconstruction (CELLR). De’Vaun has Ollier disease, a rare condition in which masses of benign cartilage, or enchondromas, grow in the bones. De’Vaun also developed genu valgum, or knock-knee, which caused his left leg to curve inward and become shorter than his right leg.

“We had no idea what Ollier disease was,” says Kristen, De’Vaun’s mother. “We felt shocked and scared, wondering how this happened or what we did to cause this. However, we knew Scottish Rite could help us.”

A multidisciplinary approach is key to supporting De’Vaun’s physical and emotional well-being. His care team includes CELLR Clinical Director David A. Podeszwa, M.D., Emily Elerson, R.N., pediatric psychologist Whitney M. Herge, Ph.D., and physical therapist Stephanie Conti, P.T. After many discussions with De’Vaun and his family, Dr. Podeszwa treated his condition by applying an external fixator to De’Vaun’s left thigh bone. The device helps gradually straighten and lengthen his thigh bone over time.

“Correcting a deformity or lengthening a limb with an external fixator is a process in which the surgery is just one part,” Dr. Podeszwa says. “The CELLR team takes the time to explain what we are doing and how we will treat the child and their family. A child won’t know what an external fixator feels like until we apply it, so the key is preparing them for it.”

Since getting his external fixator applied, De’Vaun’s family shares that his confidence has returned. He is always excited to visit his care team to show how strong he has gotten. With the help of physical therapy, De’Vaun has progressed from using a wheelchair to using a walker to walking independently. Now, De’Vaun looks forward to getting his fixator removed!

“The whole team is literally our family,” Kristen says. “They have given us a level of support we cannot believe. They genuinely care for De’Vaun as if he is a child of their own. I couldn’t have asked for a better set of people to be in our lives.”

Get to Know Our Staff: Eddie Krische, Orthotics & Prosthetics

Get to Know Our Staff: Eddie Krische, Orthotics & Prosthetics

What is your job title/your role at Scottish Rite?
I am a pediatric orthotist and prosthetist, which means I am basically part engineer, part problem solver and part cheerleader for children who are learning to move in new ways.

What is the most fulfilling part of your job?
I enjoy helping children gain their independence and confidence with their new devices. There is nothing like seeing a child take off running in their new orthosis or prosthesis.

What makes Scottish Rite a special place to you?
Scottish Rite feels like a family. Everyone is focused on taking care of the children first, and that energy is contagious. Plus, it is one of the few places where collaboration across so many different specialties happens every day under the same roof.

What made you choose a career in health care?
I chose Orthotics & Prosthetics because I wanted to design devices for patients directly without having to be in a research lab or behind a machine. Also, I like getting to know people, learn their stories and have a good laugh with anyone who comes by.

What is something unique you get to do in your position?
Recently, I have tried to blend high-tech tools, like 3D printing and AI, with old school craftmanship to create customized devices. In our department, we are trying to figure out how we can best serve our patients daily. To do that requires a bit of engineering, artistry and detective work.

What’s your favorite thing to do outside of work?
I like to watch all the New York sports (#Let’sGoMets, #Let’sGoJets, #Let’sGoKnicks and #Let’sGoIslanders). I also like to hit the gym, tinker with my 3D printer and find the coolest spots to hang out with my friends.

Do you have any hidden talents?
In high school, my family guilted me into joining a pipe band. I really wanted to play the drums, but they only had spots left for bagpipe players. I learned how to play the bagpipes, and I must admit that it was pretty cool. We marched down 5th Avenue every year, depending on the weather.

Where are you from, and what brought you to DFW?
I am originally from Long Island, New York, which is right outside of Queens, New York. I initially came to Texas to run away from the snow and freezing winters, but it seems like that weather has followed me here. I chose to stay in DFW because of the awesome people I have met and the great community around me.

If you could travel to anywhere in the world, where would you go and why?
Anywhere with a beach would make me happy.

If you had to pick one meal to eat for the rest of your life, what would it be?
Pizza from Umberto’s of New Hyde Park, New York. No, Chicago pizza is not a real pizza.

What movie do you think everyone should watch at least once?
This is not a movie, but “Ted Lasso” is a definite must-see for everyone.

What is the first concert you attended?
My first concert was U2. The best concerts I have ever gone to are a three-way tie between Luke Combs, Zach Bryan or Taylor Swift.

If you were to have a movie based on your life, which actress/actor would you choose to play your character?
I would pick Chris Pratt. He is goofy enough, but he can still pull off serious moments.

What is some advice you would give your younger self, OR what’s the best piece of advice you’ve received?
“Don’t overcomplicate the small stuff,” says Dwight Putnam, who is my great mentor, friend and brother.

Building Connections Through the Hand in Hand Support Group

Building Connections Through the Hand in Hand Support Group

When the first Hand in Hand Support Group met in April 2024, about 60 people gathered to connect, share stories and support one another. A little over a year later, that number has more than doubled.

Families primarily come from the Dallas–Fort Worth area, but some travel from San Antonio and Lubbock and even from neighboring states like Oklahoma and Louisiana. This incredible growth reflects the power of community.

Founded and directed by Scottish Rite for Children occupational therapist Amy Sitabkhan, O.T.R., O.T.D., the group offers a welcoming space for children with congenital hand differences and their families to connect, including children from birth to 8 years old.

“Typically, when families come into clinic, they’re asking similar questions,” Amy says. “They want the best for their child, and they are curious about how life will look as their child grows older — if they’re going to make friends, if they will be able to play sports and whether they’ll face bullying. I created the support group alongside my fellow occupational therapists and nurses as a way for families to build a community and have an opportunity to ask those questions, seek resources and normalize having an upper limb difference.”

The Hand in Hand Support Group also helps bridge the gap for parents of younger children and babies, offering an opportunity to network and find encouragement even before their children are old enough for Hand camp.

Between guest speaker sessions, families enjoy coffee chats and small group discussions, connect with adults who have hand differences and share their lived experiences.

For occupational therapist Lucy Ericson, O.T.R., C.H.T., the support group provides a meaningful way to connect with families beyond the clinic walls.

“It’s a rewarding opportunity to learn from others, share resources and empower families,” Lucy says.

From its humble beginnings to its rapid growth, Hand in Hand is more than just a support group — it’s a community of hope, learning and shared strength.

Healio: Scottish Rite for Children Named Best Hospital for Pediatric Orthopedics for 2025 to 2026

Healio: Scottish Rite for Children Named Best Hospital for Pediatric Orthopedics for 2025 to 2026

Healio recently featured Scottish Rite for Children in an article highlighting the hospital’s recognition in the 2025–2026 U.S. News & World Report Best Children’s Hospitals rankings. Scottish Rite earned the distinction of being ranked the No. 1 hospital in the nation for pediatric orthopedics.

“This recognition represents the heart of who we are — a team devoted to helping kids grow stronger and live healthier lives,” Daniel J. Sucato, MD, MS, chief of staff at Scottish Rite for Children, told Healio. “Whether it is in our hallways, the exam room or the OR, every interaction reflects our commitment to making a lasting difference for children and their families.”

The rankings were based on surveys from thousands of pediatric specialists, which scored hospitals on success in treating complex pediatric conditions such as fractures, scoliosis, spina bifida, sports injuries, surgical complications and infection prevention.

“I want to extend a big thank-you to our amazing team of doctors, nurses, researchers and staff members who put kids first every day,” Sucato said. “Their passion for helping children thrive drives everything we do, and it is what we believe truly sets Scottish Rite apart.”

Read the full article here.

Noah Dunks on Osteochondritis Dissecans of the Knee

Noah Dunks on Osteochondritis Dissecans of the Knee

Cover story previously published in Rite Up, 2025 – Issue 3.

by Kristi Shewmaker

It happened after school. At an innocent game of touch football, Noah was tackled from behind. He never saw it coming. At just 11 years old, Noah’s knee pain began.

A bone bruise in his right knee was the first diagnosis he received. Noah’s physical therapist questioned the diagnosis because he was not progressing, and he lost muscle. His pain eventually waned, but as he grew over the years, the pain increased. One day at baseball practice while going after a ball, he winced in pain.

“We got into the car, and he just bawled and bawled,” says Philip, Noah’s father. “Just the look on his face — I could see his despair, his helplessness to the pain.” At the time, Noah and his family lived in the Houston area. His parents took him to one doctor after another. Finally, a doctor diagnosed him with osteochondritis dissecans (OCD), a joint condition in which bone underneath the cartilage softens due to an interruption in the blood supply.

A rare condition that affects less than one percent of the population, OCD occurs most often in children and adolescents, particularly when a child is growing. It affects boys more commonly than girls, and it can occur in joints such as the ankle and elbow but is most often found in the knee. The cause of OCD is unknown, but it can be associated with injuries, as well as longterm repetitive impact to the joint. Many physicians never see a child with OCD, and some treat only a few cases per year.

After receiving this diagnosis at age 14, Noah was scared. He had played multiple sports since he was 4. “The older I got, the worse the pain got, and I couldn’t tolerate it anymore,” he says. “I thought, ‘I’m going to be 18 and not be able to play sports.’”

Noah’s family was told his treatment would most likely require many surgeries and would cost a minimum of $100,000. “We thought we were going to have to refinance our house,” says Brooke, Noah’s mother. Researching OCD online, she stayed up late into the middle of many nights reading medical articles and creating a short list of physicians who specialize in treating the condition. Noah’s family seriously considered moving to Germany for the summer so he could get treatment for a third of the price from a specialist there.

Fortunately, they did not have to move overseas because they found an expert in Texas. Brooke discovered Henry B. Ellis, M.D., pediatric orthopedic surgeon and medical director of clinical research at Scottish Rite for Children Orthopedic and Sports Medicine Center in Frisco.

She found Dr. Ellis by reading articles that he published through his collaborative research with the international Research in OsteoChondritis of the Knee (ROCK) study group. “I also found some social media parent groups who said, ‘If your doctor’s not a ROCK doctor, find a ROCK doctor,’” Brooke says. “They provide the gold standard of treatment.”

She found Dr. Ellis by reading articles that he published through his collaborative research with the international Research in OsteoChondritis of the Knee (ROCK) study group. “I also found some social media parent groups who said, ‘If your doctor’s not a ROCK doctor, find a ROCK doctor,’” Brooke says. “They provide the gold standard of treatment.”

Currently, Dr. Ellis is chair of the ROCK research committee and will be president of the group next year. ROCK has enrolled approximately 2,500 OCD cases in its database, and Scottish Rite for Children is one of the highest contributing institutions. “At Scottish Rite, we take care of well over 100
kids a year with OCD,” Dr. Ellis says, “and that’s not just surgical treatment.” OCD can also be treated nonoperatively if it is caught early enough during the progression of the condition.

Two weeks later, Noah and his family drove from Houston to Scottish Rite’s Frisco campus for the first time to meet Dr. Ellis. He recommended that Noah undergo surgery and scheduled it for later that month. “I felt at ease because I straight ahead asked him, ‘How many of these surgeries have you done?’” Philip says. “And he was like, ‘I just operated on a similar young athlete with a similar OCD this morning.’”

Though OCD surgery is a routine procedure for Dr. Ellis, Brooke emphasizes he also customized a treatment plan to meet Noah’s specific needs. “Dr. Ellis’ goals for Noah aligned with Noah’s goals,” she says. “He was going to do everything he could to get Noah back to where he wanted to be, and we had faith in him.”
In the car on the way home, Philip asked Noah what he thought, and Noah said that Dr. Ellis actually seemed to care about his knee. The icing on the cake was when the family learned they were accepted for Crayon Care, Scottish Rite’s charity care and financial assistance program. “All these things we thought were going to be such a burden for our family — Scottish Rite took care of it all,” Brooke says.

A few weeks later, Noah underwent surgery. “When we first looked at Noah’s knee, we were concerned that it would not heal without surgery because the lesion looked unstable,” Dr. Ellis says. An OCD lesion is the portion of bone underneath the cartilage that is damaged due to a lack of blood supply. If an OCD lesion is caught early, the body can typically heal the bone itself with three to 12 months of decreased activity and rest. However, an OCD lesion becomes unstable when the body starts rejecting the damaged bone. “Noah’s body was turning the bone into fibrous tissue, which is very much like dead bone,” Dr. Ellis says. “We recognized that his body would likely continue to deteriorate and not heal.”

In surgery, Dr. Ellis removed the cartilage in Noah’s knee to clean out the unhealthy bone underneath it. Then, he replaced the dead bone with healthy bone that he took from Noah’s pelvis. Using a suture bridge technique, Dr. Ellis put the cartilage back on the bone. For four months, Noah recovered and healed before Dr. Ellis went back in to remove the sutures.

Noah came out of his second surgery in a long leg brace locked in extension. He began physical therapy near his home in the Houston area and would gradually return to activities over many months. After one year, Dr. Ellis released Noah, allowing him to return to full activities without restrictions. At his two-year post-op appointment, Noah’s X-rays demonstrated there was no OCD in his knee.

“Noah progressed as we expected,” Dr. Ellis says. “Some kids receive a diagnosis, and they’re crushed. Noah is a resilient fighter type, both mentally and physically, where he was like, ‘Let’s get this fixed so I can move on.’”

Today, Noah plays football, baseball and basketball, but he is leaning toward a future in basketball, hoping to get a college scholarship and maybe even go pro. As a junior on his high school varsity basketball team, he moves between power forward and center. He also has a pretty mean shooting game. Noah told his clinical team that when his treatment was over, he was going to “dunk on it.” In May after his two-year post-op appointment, that is exactly what he did. “When I got up there and punched it through, I was like, ‘I did it!’” Noah says.

Thinking back on Noah’s time at Scottish Rite, Brooke says, “It’s just a blessing to be where we are.” Philip agrees. “I’m not going to lie,” he says. “I was worried sick about a surgeon chopping on Noah’s knee, but Scottish Rite has definitely been a godsend. They have covered us in every aspect, enabled us to take care of our child and not leave us in a spot where we have to sell everything.”

Noah says that his experience at Scottish Rite gave him hope. “Some people have not been as fortunate as me to find a surgeon who can do what needs to be done well,” he says. “Scottish Rite helped me to value the time that I have, that I’m getting a chance to play sports again, and that I need to do it the best that I can.”