Lucy's joints

Lucy has had problems with her legs for as long as I can remember. Even as a baby the only way we could calm her sometimes was by massaging her legs, or moving them in a bicycle motion. We thought it was to ease colic, no I think maybe it was leg pain all along. I took her to the GP several times and eventually she was sent to hospital for an x-ray. Nothing showed up but they did say she was hypermobile or double jointed. It was suggested she may have juvenile arthritis but on mentioning this to the GP I was told I would just be following up an unnecessary diagnosis as there wouldn't be anything they could do for her. Dismayed by the GP I went home, got Lucy a bottle of calpol and a couple of wheat bags. This helped for a while.

When Lucy was referred to a psychologist for a diagnosis into her autism she was sent for a physiotherapy check. Here her hypermobility was picked up again and it was suggested that this was what was causing the pain in her legs. So she was given regular physiotherapy which took place at school so it didn't interrupt her school life so much. She was also referred to a podiatrist who prescribed inserts for her shoes. I have noticed a difference, but she still gets pain. Recently I bought her a new game for her Wii. She loves dancing, so I bought Just Dance3. She has really enjoyed playing/dancing and it's giving her loads of exercise. Just like mum she lacks rhythm but I am already seeing an improvement. Maybe learning to dance this way will give her more poise and stop her looking so clumsy all the time? 

Looking more into Hypermobility Syndrome I have realised that Lucy has inherited this from me. I have always known that I was double jointed, but never really associated it with the pain I get. From a very young age I can remember screaming with pain in my legs and my mum massaging me. She always said it was cramp or growing pains, she had no reason to think otherwise. I still get the pain now, and in my ankles and fingers. Some times it's not so bad, sometimes it's inscrutable, but it's something I've had for such a long time I just get on with it now. The only thing I can liken the pain to is the the cramp you get during pregnancy, the sort that has you jumping out of bed in the middle of the night and will only go away by massage or walking it off. Sometimes my fingers seize up dead straight, this is painful too and I look like someone with arthritis. I can remember my nan's fingers like this, to the point when she was very old that a couple of her fingers where 'stuck' like it. Was it arthritis or did she have hypermobility syndrome too?

I have also learnt recently that bruising easily, sensitive skin and drooping eyelids are all symptoms that can be associated with Hypermobility Syndrome, both Lucy and myself have these too.