a child in a wheelchair holding a beach ball

Anaya Advances with Osteogenesis Imperfecta

Anaya attends school after pediatric orthopedic care changed her life.

Shriners Children’s expertise in rare orthopedic conditions can be life‑changing – so much so that some families travel from around the globe for care.

Anaya’s journey from Pakistan to Shriners Children’s Chicago started in 2023 for multiple surgeries on her legs, and she recently returned for more treatment. The 11-year-old was so moved by her time at Shriners Chicago that it has inspired her to pay it forward someday and become a doctor or scientist.

Anaya was born with osteogenesis imperfecta (OI), an inherited and rare brittle bone disease, which can cause soft bones that break or fracture easily.

“When she was born, she was with eight fractures (in) her legs and also in both arms,” said her dad, Muhammad.

For the first nine years of Anaya’s life, she was unable to sit up due to the effects of her OI. She was also unable to attend school in person, so her family home-schooled her. She managed to learn English by watching YouTube videos in bed. In 2023, her parents made the decision to travel abroad to Shriners Children’s to find hope and the OI care that Anaya needed to thrive.

Our healthcare system is known for being a leader in treating this condition. In the 1950s, Shriners Chicago physicians developed the first surgically-successful treatment for the disorder, known as bone rodding, which is still in use today. Shriners Children’s is also on the leading edge of OI research and is actively working toward additional innovative treatment options to help children with OI.

Peter Smith, M.D., a pediatric orthopedic surgeon who leads the OI program at Shriners Children's Chicago, performed four rodding surgeries in 2023 on Anaya. She also had physical and occupational therapy, where she slowly and carefully built up the strength to sit up and later scoot.

After those rodding surgeries, something else life-altering happened. She was able to go to school, a topic that makes Muhammad emotional – but as Anaya puts it, they are “tears of joy.”

Here, the doctors not only treat the patient, but they also treat the children just like their own children.
Muhammad, dad of Shriners Children's Chicago patient

In late 2025, Anaya and her family returned to Shriners Children’s Chicago for scoliosis treatment. First, our pediatric spine team used halo gravity traction, a method that gently stretches and straightens the spine. Then she underwent spinal fusion surgery in early 2026.

She continues to work with the rehabilitation teams, wearing a plastic brace to protect her back as it heals. She and her family will return to Shriners Children's Chicago for more therapy in the future.

“My experience with Shriners has been amazing!” said Anaya. “If you know anyone who has osteogenesis imperfecta, that's not getting treatment, contact Shriners. They can help in any way possible.”

Anaya's Story – Shriners Children's Treatments Allowed Her to Go to School

Anaya first came to Shriners Children's Chicago from her home country of Pakistan, three years ago for multiple orthopedic surgeries on her legs. She was born with osteogenesis imperfecta, a brittle bone disease, which caused 8 fractures at birth. Since those surgeries in 2023, at the age of 9, she's been able to sit up and go to school for the first time. Now in 2026, she and her family returned to Shriners for Halo gravity traction treatment and spinal fusion surgery to help her scoliosis.
View Transcript
Speaker 1:

Hi, honey.

 

Anaya, Patient with Osteogenesis Imperfecta:

Hello.

 

Speaker 3:

This is Anaya.

 

Anaya, Patient with Osteogenesis Imperfecta:

I am 11, turning 12 October 15th.

 

Speaker 3:

Her journey is a patient one that's led her to Shriners Children's Chicago.

[text on screen: My experience with Shriners has been amazing.]

Anaya, Patient with Osteogenesis Imperfecta:

My experience with Shriners has been amazing.

 

Speaker 3:

Her time at our hospital started in 2023. For the first nine years of her life, she wasn't able to sit up. Born with osteogenesis imperfecta, a brittle bone disease in a condition Shriners Children's has led the way for treatment and research.

[Images of an infant labeled 2016 and 2015 appear on screen]

[text on screen: She was with eight fractures in her legs and also in both arms.]

Speaker 4:

She was with eight fractures in her legs and also in both arms.

 

Speaker 3:

Three years ago, the family traveled from Pakistan for four rodding surgeries on Anaya's legs.

[text on screen: After the first surgery, then she became able to go to school. So it was really...]

Speaker 4:

After the first surgery, then she became able to go to school. So it was really...

 

Speaker 3:

Anaya, being able to go to school for the first time in her life was emotional for the whole family.

[text on screen: Your child that is disabled going to school for the first time, it will make you very happy, but also emotional at the same time. It's like something called tears of joy.]

 

Anaya, Patient with Osteogenesis Imperfecta:

Your child that is disabled going to school for the first time, it will make you very happy, but also emotional at the same time. It's like something called tears of joy.

 

Speaker 3:

She and her family are now staying at the Ronald McDonald House for a few weeks, after she came back to our hospital recently for a spinal fusion surgery due to her scoliosis.

[text on screen: We are very grateful, because here, the doctors not only treat the patient, but they also treat the children just like their own children.]

Speaker 4:

We are very grateful, because here, the doctors not only treat the patient, but they also treat the children just like their own children.

 

Speaker 3:

After her time at Shriners Children's, she wants to achieve her extraordinary, and become a doctor or scientist, or maybe an ambassador.

[text on screen: If you know anyone with osteogenesis imperfecta that's not getting treatment, contact Shriners. They can help in any way possible.]

Anaya, Patient with Osteogenesis Imperfecta:

If you know anyone with osteogenesis imperfecta that's not getting treatment, contact Shriners. They can help in any way possible.

 

Speaker 4 and Anaya together:

Bye.

[Shiners Children's Chicago logo]

Anaya Is Thriving Thanks to Pediatric Orthopedic Care and Therapy

Anaya has made progress thanks to surgery, medications, and therapy provided by the staff at Shriners Children's.

a man sitting on a couch next to a child in a wheelchair

Anaya and her dad sit together at the Ronald McDonald House.

a child sitting up with the assistance of an adult

Anaya sits up for the first time during a 2023 occupational therapy session.

two women helping a child float in a pool

Anaya safely stands up during water therapy.

a woman kneeling next to a child holding a plant

Anaya holds an aloe plant during horticultural therapy.

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