The blog in which I try to explain how it feels to be the parent of a child coping with regular dislocations.

June 2012 (updated 2019)

Some time ago, I was asked by a health practitioner, to explain ‘how it feels’ to look after a child with a complex form of hypermobile Ehlers-Danlos Syndrome. She wanted those without the condition, to gain an insight, even if just for a few moments, of the impact the frequent injuries (one of the many features of the condition), can have on family life. Here I try to explain…

 

This blog is in the process of being updated

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