Hello,
This blog is an informative tool for parents by parents.
not meant to substitute for the medical diagnosis that only a pediatric neurosurgeon can do with competence and confidence.
But how small group of parents, former child-operated, and supporters, created on Facebook, we also extend our views to surfers who are not enrolled in that social network.
My job is to act as a summary and report the information coming to light and it seems more important.
If you want to come visit us on fb also join the group Facebook:
Diseases rare: the craniosynostosis
or become fan of this page:
craniosynostosis: children more than rare ... SPECIAL
On this page you will find some of our stories and news that we feel are most important.
you soon!
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