Scoliosis is a condition that is surprisingly common amongst adolescents, yet is little known about. My parents, no doubt like many others, had some name recognition, but had no idea what it was.
What is important, although it took them some time to learn, is that you are not alone.
The Scoliosis Association UK is a patient support organisation for people with scoliosis and their families; providing advice, support and information. Part of this network is Princess Eugenie, who became the Royal Patron of SAUK in October 2020.
In the context of the wonderful treatment she received at the Royal National Orthopaedic Hospital, Princess Eugenie recently said: “In 2002, when I was 12 years old, I was diagnosed with scoliosis, and told I would need corrective surgery. This was, of course, a scary prospect for a 12 year-old; I can still remember how nervous I felt in the days and weeks before the operation. During my operation, which took eight hours,... ”.
At the time a Buckingham Palace spokeswomen told BBC News Online that: “Princess Eugenie will be having a very minor routine operation”.
We now live in a more open society and her scoliosis journey offers inspiration and encouragement to people who are struggling with a diagnosis. The Scoliosis Association is there to help.
Natalie Cooper, a Scoliosis Association representative, explains SAUK's aim.
If you or anyone you know has been affected by scoliosis visit Scoliosis Association UK or call their helpline on 0208 964 1166 for support and advice.
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