Many of us parents, to have sought information across hospital, Internet, associations of parents of hospitalized children, doctors and surgeons. All that gleans from it, and there, is a bit "messy," it must be said. So it would be good to find a place to "put everything in common" because it is more concerned parents to bring their experience the better you lighten our difficulties.
For making this journey with my son, ten years ago and at a time when information was reduced on the separate question for the experts, I felt that I could be helpful to parents who have a child with hypoplasia of one or more members by giving them a space for exchange and dialogue and by sharing an experience that, with hindsight, may benefit others.
I came into contact with some people concerned and WADA was born.
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