The Pattern of Perseverance: How Scoliosis Fueled Gabbi’s Passion for Fashion

The Pattern of Perseverance: How Scoliosis Fueled Gabbi’s Passion for Fashion

Hidden in every seam of a garment is a unique story, as 21-year-old Gabbi would discover. While she has always loved fashion, Gabbi’s appreciation for design would develop in the most unexpected places — from her own scoliosis journey. “I always follow the wise words of Coco Chanel that beauty begins the moment you decide to be yourself,” Gabbi says. “Fashion is where individuals can express themselves through their own ideas of creativity.”

At age 15, Gabbi and her family were referred to Scottish Rite for Children for a scoliosis evaluation. Certified physician assistant Jessica Landson, P.A.-C., diagnosed her with adolescent idiopathic scoliosis (AIS) of the thoracic, or upper spine, region. AIS is the most common form of scoliosis that affects children and teens between the ages of 10 to 18 with no known cause.

In Gabbi’s case, her diagnosis affected more than just her physical well-being. While she had asymmetry in her waist and shoulders, she also developed a sense of body dysmorphia. Body dysmorphia is a mental health symptom that occurs when someone experiences negative emotions and/or hyper focuses on a real or perceived flaw in their appearance.

“Not only was I struggling on the inside, but I also struggled on the outside,” Gabbi says. “I was in constant pain because of how my scoliosis affected my ribs. I felt ‘big’ because of the way my back lumped from my curved spine.”

To correct Gabbi’s curve that had grown to 51 degrees, pediatric orthopedic surgeon and Assistant Chief of Staff Brandon A. Ramo, M.D., performed a spinal fusion. The procedure kick-started her healing journey from the inside out, helping not only her condition but also her body dysmorphia.  

“My experience at Scottish Rite was incredible,” Gabbi says. “Dr. Ramo is one of my favorite surgeons of all time. He has this calming aura around him, and he made my surgery a breeze in all aspects.”

After surgery, Gabbi explored her passion for fashion through her studies. She majored in apparel design and marketing at the University of Arkansas. For her school’s final project, Gabbi showcased her care journey with scoliosis through fashion in the form of creating a dress.

“The idea of the dress came to me because we had to create something that impacted our lives,” Gabbi says. “The significance of this garment is very important to me because I didn’t know the full extent of my body dysmorphia until after my surgery.”

Gabbi’s project consisted of a long formfitting dress to display the curve of her spine. The garment incorporated personal touches of herself, from the ruffles that represent the preoperative curve of her spine to the green accessories that represent the honorary color of Scoliosis Awareness Month. After a semester of hard work, Gabbi walked down the runway at her school’s fashion show. In that definitive moment, she describes feeling powerful.

“Designing this dress went beyond my everyday love for fashion,” Gabbi says. “I felt like I was bringing light to something that is a struggle behind closed doors. It truly was a life-changing moment because I realized that my journey was not for nothing. I knew that night that this was truly an impact — not just for myself, but others.”

Today, Gabbi is looking forward to where the fashion design industry will take her. She shares that the care she received at Scottish Rite is paramount to building her self-confidence. “Scottish Rite means the world to me,” Gabbi says. “Not only did my care change a physical issue I had, but it changed my life. Scottish Rite helped me become the best version of myself.”

 Do you have a story? We want to hear it! Share your story with us.

5 Common Types of Scoliosis: Which Form Does Your Child Have?

5 Common Types of Scoliosis: Which Form Does Your Child Have?

Scoliosis is a common orthopedic condition that affects between 2% to 3% of the population. This abnormal sideways curvature of the spine can range from mild to severe, with varying health impacts. Scoliosis must be monitored until children stop growing, and moderate to severe curves will need corrective treatment. However, different types of scoliosis have different prognoses and may require different types of treatment.

What Is Scoliosis?

Prior to learning about the different forms of scoliosis, it helps to first understand what this condition is and how any form of the disease can affect a child.

Scoliosis happens when a child’s spine curves sideways. Normally, the spine is straight or has a slight S-curve when you look at it from the side — the top of a child’s back may curve out a little bit, and their lower back may curve in slightly. In children with scoliosis, the spine curves or twists in an S- or C-shape.

Mild cases may only limit a child’s flexibility, but severe cases can cause deformities and serious health problems, such as:

  • Arthritis
  • Back pain
  • Breathing problems or other lung issues
  • Heart problems
  • Paralysis
  • Problems walking, standing or doing other physical activities

Whether mild or severe, the form of scoliosis your child has can also play a role in its long-term impacts. Below are five common types of scoliosis.

Idiopathic Scoliosis

Idiopathic scoliosis, also called adolescent idiopathic scoliosis, is the most common type of scoliosis. It affects around 80% of children with scoliosis. It typically shows up at age 10 or later and has no known cause, although there is a genetic connection. About 30% of children with idiopathic scoliosis have a family history of scoliosis. Despite what many parents or kids may think, carrying a heavy backpack or slouching will not cause scoliosis.

Treatment for this type of scoliosis depends on the severity of your child’s spinal curve, defined as:

  • Mild, less than 20 degrees
  • Moderate, between 25 degrees and 40 degrees
  • Severe, greater than 50 degrees

Regardless of severity, many children with scoliosis benefit from physical therapy (PT). PT helps reduce pain and improve breathing, while also preventing a curve from getting worse.

Children with mild curves may simply need monitoring every six to 12 months to ensure a curve is not getting worse. Moderate curves may require a child to wear an orthotic back brace daily for months or even years.

Braces are usually successful in stopping the curve from progressing to a point of needing surgery. Severe curves or moderate curves that do not get better with bracing may require spinal surgery. Spinal fusion is the most common type of surgery for severe adolescent idiopathic scoliosis, but some patients may benefit from a newer technique, vertebral body tethering (VBT).

Congenital Scoliosis

Congenital scoliosis is a form of the condition that exists when a child is born. A rare birth defect, congenital scoliosis occurs in only 1 in 10,000 children. There are several different types of congenital scoliosis, each affecting how the spine curves abnormally in different ways. All can cause serious problems in children’s growth.

Many children with congenital scoliosis are not diagnosed until the problem becomes noticeable later in childhood or during the teenage years. Unlike idiopathic scoliosis, congenital scoliosis usually cannot be helped by bracing. Children with mild curves will still likely only need monitoring, but those with moderate to severe curves may need surgery.

Neuromuscular Scoliosis

Neuromuscular scoliosis is caused by medical conditions that impact the muscular or neurological systems. These conditions can affect a child’s muscle balance or how the body controls the muscles that support the spine.

Common neuromuscular conditions that lead to scoliosis include:

  • Cerebral palsy
  • Friedreich ataxia
  • Muscular dystrophy, especially Duchenne
  • Myelodysplasia
  • Spina bifida
  • Spinal muscle atrophy
  • Spinal trauma, especially that causing paralysis

These conditions may require children with scoliosis to be in wheelchairs. For those children, wheelchair seats can be modified to improve balance.

Bracing may also help many patients with neuromuscular scoliosis, but it will not stop the progression of curves. Surgery may be an option, depending on the underlying medical condition and other factors.

Early-Onset Scoliosis

Early-onset scoliosis develops before age 10. In most cases, early-onset scoliosis is idiopathic. Treatment is crucial for preventing breathing problems or deformities later in life.

Infants and children younger than age 2 who have early-onset scoliosis may need to wear a cast for two to three months at a time. In children this young, casting is often easier than bracing.

If a very young child’s scoliosis is severe, they may need a special type of surgery that involves attaching a magnetic rod to the spine. The rod can be lengthened as the child gets older, at which point they usually have spinal fusion surgery.

Syndromic Scoliosis

This type of scoliosis is very rare and develops as part of another condition, such as:

  • A connective tissue disorder, such as Marfan or Ehlers-Danlos syndrome
  • Beale’s syndrome
  • Down syndrome
  • Prader-Willi syndrome
  • Rett syndrome

Treatment options for syndromic scoliosis depend on the severity and the other health conditions involved.

Could Your Child Have Scoliosis?

Children are usually screened for scoliosis during their annual wellness exams, and they may be screened at other times, such as during school health screenings.

However, children grow quickly, so it’s important for parents to know the symptoms of scoliosis. Be on the lookout for signs such as:

  • Back pain
  • One shoulder blade that sticks out more than the other
  • One shoulder, hip bone or rib cage that seems higher than the other
  • Rounded shoulders
  • The sense that your child’s head is no longer directly centered above the pelvis
  • A sunken chest

Call your child’s pediatrician if your child experiences any of these symptoms or if you notice an unusual spinal curve when your child bends forward to touch their toes. Getting treatment early, no matter which type of scoliosis your child has, often leads to more successful outcomes.

If your child has been diagnosed with scoliosis, the Scottish Rite Center for Excellence in Spine is here to help. Schedule an appointment to discuss scoliosis care.

Scoliosis Awareness Month: What is Scoliosis?

Scoliosis Awareness Month: What is Scoliosis?

What is scoliosis?

Scoliosis is not a disease. It is an abnormal curvature of the spine. In addition to the spine curving sideways, it also twists, making the ribs (which are attached to the spine) look uneven. This may cause a prominence or a “bump” on the back. Other signs include a shoulder or hip that looks higher than the other or the chest may appear uneven. Scoliosis is usually a painless condition. Children with scoliosis are no more likely than kids without scoliosis to have back pain.

The diagnosis of scoliosis is confirmed by taking an X‐ray of the spine. If a curve measures more than 10 degrees, it is called scoliosis.

Who has it?

Scoliosis usually occurs in early adolescence and becomes more noticeable during a growth spurt. Approximately 0.5 percent of young people develop scoliosis that requires treatment. Girls have scoliosis eight times more often than boys. Sometimes scoliosis can be found in several family members, for several generations.

Why does it happen?

There are several different types of scoliosis that affect children.

Idiopathic Scoliosis
The most common type of scoliosis is idiopathic, which means the exact cause is not known. Idiopathic scoliosis can occur in infants, toddlers and young children, but the majority of cases occur from age 10 to the time a child is fully grown. Scoliosis tends to run in families. It is not a disease that is caught from someone else like a cold. There is nothing you could have done to prevent it. It is not caused by carrying heavy books, backpacks or purses, slouching, sleeping wrong or from a lack of calcium.

Congenital scoliosis
Congenital means that you are born with the condition. Congenital scoliosis starts at the spine forms very early in pregnancy. Part of one or more of the vertebra does not form completely, or the vertebra does not separate properly. Other abnormalities may also be present such as ribs may be missing or there can be ribs that are fused together. This type of scoliosis can be associated with other health issues including heart and kidney problems.

Neuromuscular scoliosis
Any medical condition that affects the muscles and the nerves can lead to scoliosis and this is known as neuromuscular scoliosis. This is most commonly due to muscle imbalance and/or weakness. Examples of neuromuscular conditions that can lead to scoliosis include cerebral palsy, spina bifida and muscular dystrophy.

How is it found?

Finding scoliosis is easy when the back is examined closely but it can be missed if someone isn’t looking for it. Parents or friends might notice the curve, but most curves are found through a school screening program or by a pediatrician. A trained examiner can detect even a slight curve when a person bends over to touch her or his toes. If a curve is suspected, a referral is often made to an orthopedic doctor. Print this PDF.

What may be noticed on someone who has scoliosis:
  1. One shoulder may be higher than the other.
  2. One scapula (shoulder blade) may be higher or more prominent than the other.
  3. When the arms hang loosely at the side of the body, there may be more space between the arm and the body on one side.
  4. One hip may appear to be higher than the other.
  5. The head may not be centered exactly over the pelvis.
  6. The waist may be flattened on one side; skin creases may be present on one side of the waist.
What are the types of curves?

Curves occur in the spine between the neck and the pelvis. They are named depending on their location. The most common type is in the upper back (thoracic) and tends to curve to the right. Other curves are in the lower (lumbar) spine. Many children have both types of curves.

How are curves treated?

Treatment depends on how big the curve is when it’s detected and how much growth is left. Curves can worsen during the major growth spurts. Curves less than 20 degrees may not need any treatment except to be checked by the doctor from time to time until the child has stopped growing.

If a child is still growing and the curve is greater than 20 degrees, the doctor might recommend wearing a brace. Bracing will not correct a curve. The goal of bracing is to help prevent the curve from getting worse during growth. Braces must be worn as prescribed by the doctor during the growing years in order to be effective. After growth is completed or if the curve does not respond to bracing, the brace is no longer worn.

If a curve is advanced, the doctor may suggest an operation to correct the scoliosis. Allowing a large curve to progress could interfere with heart and lung function in later years. The most common type of operation is called posterior spinal instrumentation and fusion. Instrumentation refers to metal rods and screws that are attached to the spine to hold it in the corrected position. Fusion refers to the bone graft that is placed along the spine making the vertebrae one solid piece.

Learn more about the importance of scoliosis screening.

News On 6: Tulsa Man Sells Mustang to Support Scottish Rite for Children

News On 6: Tulsa Man Sells Mustang to Support Scottish Rite for Children

More than 50 years ago, Bryan Rowland was a patient at Scottish Rite for Children. Bryan was born with Klippel-Feil syndrome, a rare condition in which his vertebrae were fused together.

“Thankfully, my parents sought treatment through Scottish Rite, and I received corrective surgery as a toddler,” Bryan says. “They changed my life.”

Now, Bryan is giving up his beloved 1969 Ford Mustang to support the place he loves.

“It remains a magical place in my memories, a life-changing factory of fun for kids, in spite of physical challenges,” Bryan says. “Hopefully saying thank you by donating my prized car means more than just the two words.”

You can watch Bryan’s full story here.

CORA Prepares the Next Generation of Medical Experts

CORA Prepares the Next Generation of Medical Experts

Research equips Scottish Rite for Children clinicians to continuously provide the best care possible to every patient. Each year, Clinical Orthopedic Research Assistants (CORAs) are chosen to assist Scottish Rite’s team of experts in addressing a wide range of clinical needs, as well as innovating treatment options.

The CORA program serves as a patient-driven, hands-on experience for aspiring medical students. This program was created in 2022 to provide opportunities to students who aim to enhance their medical knowledge before entering medical school.

CORA staff assists Scottish Rite experts in performing clinical research tasks and collaborating on research projects. Each CORA staff member specializes in a specific area of study and works with the experts in that department, where they gain a well-rounded experience in their field of interest. CORA areas of study include Spine, Foot, Hip, Rheumatology, Neurology, Sports Medicine and Movement Science. They receive ample clinical interaction, research experience and mentorship within their field of interest, as well as other fields of their choosing.

Amareesa Robinson, a current CORA staff member, works with Scottish Rite’s spine experts. As a former Scottish Rite patient who had scoliosis, she is experiencing a full-circle moment by researching and collaborating with the spine team. She works closely with Assistant Chief of Staff Karl E. Rathjen, M.D., studying the use of tissue expanders to manage spinal deformities.

“What I love about researching spine conditions is the depth and complexity in the diagnoses and treatment methods,” Amareesa says. “Dr. Rathjen has served as a vital part of my experience and has taught me not only about research but also much about what goes into caring for patients with unique and complex conditions.”

As Amareesa’s CORA time wraps up, she is looking forward to a future in medicine. She was accepted into McGovern Medical School at UTHealth Houston. “My time at Scottish Rite has shaped the kind of physician I want to become,” Amareesa says. “I know I still have much to learn, but Scottish Rite has shown me the type of career I want to build.”

If you are interested in a career in medicine and plan to take a year or two off after college before applying to medical school, learn more about becoming a CORA at Scottish Rite careers. Applications for June 2026 positions are being accepted through spring of 2025 and can be found here

From Patient to Advocate: “The Chosen” Actor Jordan Walker Ross Inspires All

From Patient to Advocate: “The Chosen” Actor Jordan Walker Ross Inspires All

Actor, filmmaker and screenwriter Jordan Walker Ross describes Scottish Rite for Children as a place of love and hope. Shortly after Jordan was born, his family brought him to Scottish Rite for cerebral palsy (CP), which affects his muscles and movements. Jordan also developed scoliosis due to his muscle weakness. After years of undergoing multiple hip surgeries, a spinal fusion and recovery in the Inpatient Unit, Jordan recalls only positive memories at Scottish Rite.

“I felt at home at Scottish Rite, even when I was about to undergo a major surgery,” Jordan says. “There was always something happening to help the patients experience something fun and memorable, regardless of whatever pain we were feeling.”

Since age 6, Jordan performed in local theaters and professional productions. However, his condition caused him to develop a limp, which impacted his ability to receive larger roles. This changed in 2018 when Jordan was cast in the TV series “The Chosen,” a historical drama based on the life of Jesus. He plays the role of Little James, who is one of Jesus’ disciples.

“The creator of “The Chosen” made my limp part of my role,” Jordan says. “I used to hide my disability, even feeling embarrassed to call myself disabled. Now, I own it.”

The role of Little James marks a turning point for both Jordan’s career and personal life. Since the success of “The Chosen,” Jordan has received roles in other films and TV shows, like “1883,” “Yellowstone” and “Black Panther: Wakanda Forever.” He credits this to a pivotal scene in season three of “The Chosen” between Little James and Jesus, where Little James asks Jesus why he hasn’t healed him of his condition.

“It was cathartic to perform that scene and to express many frustrations that I’ve had in my life,” Jordan says. After the scene aired, he recalls that people — including patients from Scottish Rite — commented how it helped them feel seen. “I was like, ‘Why don’t I see that in myself?’” he says. “I realized that I had stopped loving myself the way I did back then. Now, I am proud of who I am and what I mean to my community.”

Jordan currently uses his platform to advocate for increased visibility of disabilities in all spaces. From his podcast to public appearances, Jordan promotes self-acceptance for all through his endeavors.

“I have no idea where I would be if it wasn’t for Scottish Rite,” Jordan says. “I refer someone any time I get the chance because Scottish Rite literally changed my life.