I thnk most people will do anything for their children and Annabelle's Challenge proves that. What sets them apart from the rest is how much they are prepared to give to the hundreds of other families all suffering with this same or similar conditions. I came across AJ and her family just as my daughter was diagnosed with EDS Hypermobility Type and it was an inspiration to read their posts on Facebook and see what they are doing. Faced with the awful truth of having a child with a life limiting illness has got to be every parents nightmare but they approach it with positivity, determination and courage. They have done so much for raising awareness of the condition and any recognition they receive is not only well deserved for them, but also serves to bring EDS in to the spotlight.
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