Something in her neck tweaked causing an excruciating amount of pain and she couldn’t move. “I first got put into traction in hospital by a specialist,” she says. “They put weights on a pulley system in an attempt to stretch my neck out. I was in hospital for about two weeks in this contraption and it was the worst possible thing that could have been done as they were putting weights on a bone that was fused to other bones.”
Urquhart was in pain, but the doctors didn’t understand exactly what was going on. It was only after Urquhart’s mother found a neurosurgeon, an expert in spinal osteoporosis anomalies, who x-rayed her at a specific angle and exposed an extra vertebra.
It was an extremely rare condition, she was one in the 600,000 people born with a spinal anomaly and at that point, the only person with her condition in the world.
“It was quite an ordeal. It took us a very long time to get an actual diagnosis because no one could see what was wrong with me or find the issue,” she says. “The neurosurgeon changed my life. He explained that it would be a lifelong issue for me and that there was no potential for surgery. I also have a high chance of paralysis because I am double-jointed.” Urquhart couldn’t play sports. If she got knocked hard enough, she could be paralyzed. “My parents freaked out. Their response was ‘oh my God, bubblewrap her’. It was scary. There was not a lot of information or cases to reference,” she adds. Urquhart found herself in medical journals and her case is still the one referenced today.
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Denne historien er fra August - September 2023-utgaven av Forbes Africa.
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