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Our Spastic Diplegia CP Journey with our 4 yo son
audiosmee
Member Posts: 1
When my son Charlie was diagnosed with CP we didn't know where to go or what to look at.
Now he is 4 and thriving, he's not quite walking but he will. We've done all sorts to give him the opportunities we could.
We've documented our journey on a blog www.charlies-dad.org in case there is anything that might be helpful to anybody.
One of the best bits of advise we were given early on is 'the more you do, the more chance he has...'
please, have read- it's our way of paying it forward...
mark, Lou and charlie
Now he is 4 and thriving, he's not quite walking but he will. We've done all sorts to give him the opportunities we could.
We've documented our journey on a blog www.charlies-dad.org in case there is anything that might be helpful to anybody.
One of the best bits of advise we were given early on is 'the more you do, the more chance he has...'
please, have read- it's our way of paying it forward...
mark, Lou and charlie
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Having a good look now, thanks for joining and showing us this.
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