I’m Caroline. I’m 27. I have hip dysplasia as well as femoral anteversion and Ehlers Danlos Syndrome. I was diagnosed with hip dysplasia at 14 when I tried to start training more seriously for sports. I initially presented with knee pain, but it was quickly discovered that I had hip dysplasia. I had my first PAO at 15.

After my PAO I still struggled with pain so also underwent a femoral derotation and labral repair. I spent more that a year on crutches trying to recover from that surgery, and finally relearned how to walk after being told I may not be able to.
I’ve essentially had the same surgeries mirrored on my other side over the last 10 years. I am currently healing from the femoral osteotomy. When I was younger, I was under the impression that, once I have surgery, I will be “fixed.” For me, that has not been the case. Hip dysplasia continues to affect my function and cause pain, and likely will for the rest of my life.


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