I am 23 years old and I was diagnosed with Clicky Hip (Hip displasia) when I was 3 weeks old I was put in a cast for 3 months to help the bone sort of repair its-self. Unfortunately 16 years down the line I started to feel in a lot of pain when walking and getting cramp in my left hip when standing. I went to my GP to see if there was anything they could give me for my pain and he prescribed me with an anti-inflammatory, I also had tests to see if it could be what my Dad has which is ankylosing spondylitis. The test results said I was clear for this but it was laying dormant and anything could trigger this. I took the anti-inflammatory these but they done nothing for the pain. After another couple of years once I had finished college I had moved and was in more and more pain everyday. I had to do something about this.
I had a search up online for my symptoms and stated I had Clicky hip when I was born and it came up with Hip dysplasia. Once I found out the name of it I researched this to see what it was. Once I had done this I knew this is what I had. I then booked myself in to see my new doctor and see what they could do for this. I had tests and x-rays to make sure this is what I had and the outcome was Hip dysplasia in my left hip. My GP referred me to have a six week coarse of physio to see if we could build the muscle up around the bones to stop some of the pain but this only made it worse. I then lost heart in getting it sorted as my GP said this is all they could do or it would be a hip replacement which they wouldn’t do now because of my age.
I researched more after 2 years as I was determined there was something I could do. I found online an operation called the PAO (Periacetabular Osteotomy) I have looked in to this operation inside out and was very interested in getting this done. I then went back to my doctor to see if there was any chance in me receiving this. They referred me to a consultant that specialised in this region and I had more x-rays and scans. Once they had a talk with me about the operation and what they can do they referred me to a surgeon in London who specialised in this operation.
I asked all the questions I had and got all the answers I needed. At the end of the consultation he asked me if I wanted to be put on the list for the PAO. I said yes as I have wanted this for a long time. I got a letter 3 weeks later confirming I was put on the list and I called the hospital to see how long the wait would be they told me it looked like October but they wanted to talk to the surgeon and a manager to see if they could get an earlier date. On the 25th April 2016 I got a call and they said my operation day is 26th May 2016. I had a Month to get ready. I was so overwhelmed and shocked as to how quick they have fit me in. I am now scared and excited at the same time as these 3 weeks are going to go very quickly.
I just wanted to know before I do this has anyone had this operation and has this made any difference? All the reviews I have read are amazing results and I just wanted to know if anyone had this a few years ago and what the effect is now. I want to know that once I have children I will be able to run around and do activities with them.
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