Woman bullied for her one-in-50,000 condition has relearned to walk 10 times after defying doctors who said she would be wheelchair-bound for LIFE
- Sarah-Louise Walker was born with nail-patella syndrome affecting her knees
- Bullies would call her ‘disabled girl’ and ‘peg leg’ as she used a wheelchair
- She had surgery throughout childhood to attach frames to her legs with pins
- Every time she has re-learnt to walk, despite being told she never would age two
A woman with a one-in-50,000 genetic condition has relearned to walk 10 times after doctors told her she would be confined to a wheelchair for life.
Sarah-Louise Walker, 24, of Middlesbrough, was born with nail-patella syndrome, which means her kneecaps are poorly developed, her elbows and hips protrude further, and she is unable to turn her hands over.
Aged two, doctors told her family that she would never walk, and she relied on a wheelchair after tirelessly trying. Bullies would call her the ‘disabled girl’ and ‘peg leg’ for being different.
She had ten operations, many of which were to attach frames to her legs with pins to try and strengthen the muscles. Her most recent was in 2012.
After every operation, with the help of her mother, Helen, 45, she has had to learn to walk again. She is now able to walk but relies on her wheelchair when she gets tired.
Sarah-Louise Walker was born with a one-in-50,000 genetic condition but has learnt to walk after doctors told her she would be confined to a wheelchair for life. Her kneecaps are poorly developed, her elbows and hips protrude further, she is unable to turn her hands over and has clubbed feet
Ms Walker has had ten operations, many of which were to attach frames to her legs with pins to try and strengthen her weak muscles
Ms Walker, now a social media manager, said she was bullied as a child due to her condition, nail-patella syndrome, which affects her kneecaps, elbows and hips
Ms Walker, pictured at age two, said she had locked legs until the age of 14 meaning she was ‘unable to bend her legs properly’
Nail-patella syndome affects people in a variety of ways. Ms Walker was diagnosed at birth after doctors discovered her auntie, grandfather and her father also had the condition. Ms Walker’s brother and sister are also affected, but to a lesser degree
Ms Walker said: ‘I have always refused to let my condition define me.
‘And my mum was a fantastic role model for me, she was determined that I would make something of my life.’
Ms Walker was diagnosed with nail-patella syndrome at birth in January 1995, after doctors discovered her auntie, grandfather and her father also had the condition.
The features of nail-patella syndrome vary in severity between affected individuals, even among members of the same family.
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The syndrome is usually caused by a fault in a gene called LMX1B which is inherited from one parent.
As a baby, Ms Walker, whose brother and sister also have the condition to a lesser degree, was forced to wear casts to support her legs.
She said: ‘I was born with missing muscle in my legs so I couldn’t bend them properly.
‘This meant they were permanently locked [in a bent position] until I was 14. Due to the lack of muscle, I was unable to walk as my legs weren’t strong enough.’
Doctors revealed that Ms Walker, then aged two, would be confined to a wheelchair for the rest of her life.
Ms Walker got tired easily as she persisted in learning to walk, needing a wheelchair. Pictured, age eight being pushed by her grandmother, Anne
Ms Walker wore casts on her legs permanently until the age of one and often thereafter
Ms Walker’s mother, Helen, always helped her daughter to walk around the house from a young age. She took her first steps age two (pictured)
She said: ‘Thankfully, mum was determined that I would be able to have as normal a life as possible.
‘After I got my casts off my legs when I was one, she kept teaching me how to walk, gently coaxing me around the house.
‘I was two when I finally took my first steps.’
Even though Ms Walker could manage a small amount of walking, she had to rely on a wheelchair as she tired easily.
Sadly, because of this, she was bullied in school. Ms Walker said: ‘I hated having to use a wheelchair but knew I had to.
‘Bullies called me “peg leg” and “disabled girl”. Being bullied upset me but I learnt to brush it off.
‘I realised that people usually act negatively when they don’t understand the circumstances.’
At the age of five, seven and 11, Ms Walker had to wear ilizarov frames, a contraption that stretched her muscles, on both legs.
Ms Walker had to wear ilizarov frames, a contraption that stretched her muscles, on both her legs. Pictured, age five wearing a frame. The frame was kept in place with pins
After wearing the frames for around four months, Ms Walker would have casts on
Ms Walker said her mother was a ‘fantastic role model’ who was ‘determined’ for her daughter
The frame was kept in place with pins through the legs, leaving Ms Walker scarred.
She said: ‘Doctors hoped that stretching my muscles would make them stronger. I wore the frames for around four months.
‘The frames were agony, doctors tightened them so they really hurt. I think my classmates called me names as they were confused about why I wore the frames.’
She added: ‘I’ve had over ten operations so far, mainly inserting the pins for the ilizarov frames.
‘And in another operation [her most recent in 2012], surgeons broke my bones in my feet to try to cure my club feet. Unfortunately this operation didn’t work.
‘I’ve had to relearn how to walk each time. It’s exhausting and I rely on help after my operations, a lot. Sometimes I do have to use my wheelchair as I get tired.’
Ms Walker credits her boyfriend, Michael Temple, 23, a manager at a guitar shop, for keeping her motivated. The couple have been together since 2016
Ms Walker, who has scars from the pins in her legs, said: ‘I’ll never let my disability hold me back’
Ms Walker hopes to work with children with mental health conditions due to her troubled childhood being bullied
Despite her condition, which has no cure, Ms Walker has a positive outlook on life. Ms Walker said: ‘I’ll never let my disability hold me back.
‘I’ll need another operation soon on my club feet, which is a common symptom of my syndrome. But I won’t let it affect me.
Due to the problems she suffered as a child, Ms Walker would like to have a career working with children who have mental health issues.
‘One day I hope to be able to ride a bike and be able to walk down the aisle on my wedding day,’ she said.
WHAT IS NAIL-PATELLA SYNDROME?
Nail-patella syndrome (NPS) is a rare genetic disorder that is usually apparent at birth or during early childhood.
Although the symptoms and physical characteristics associated with NPS may vary greatly in range and severity, characteristics include:
- Nails may be missing, underdeveloped, discoloured, split, ridged or pitted.
- The kneecaps may be missing, small, irregularly shaped and easily dislocated, and can click, lock or may feel unstable or painful.
- Some people aren’t able to fully extend their arms or turn their palms up while keeping their elbows straight. The elbows may also angle outwards, and dislocations can occur.
- Bony growths on the pelvic bone (visible on X-rays) are common, but don’t usually cause problems.
- There may be protein in the urine (an early sign of kidney problems), which can be accompanied by blood in the urine. This can sometimes progress to kidney disease.
- Increased pressure in the eyes (glaucoma) at an early age
Nail patella syndrome is usually caused by a fault in a gene called LMX1B that’s inherited from one parent.
But there isn’t always a family history of nail patella syndrome. In some cases, an LMX1B gene mutation (alteration) occurs for the first time on its own.
If you have nail patella syndrome, there’s a 1 in 2 (50%) chance that any child you have will be born with the condition.
There’s no cure for nail patella syndrome, but treatments are available to help manage the symptoms.
According to the US National Library of Medicine, the prevalence of nail-patella syndrome is estimated to be 1 in 50,000 individuals.
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