Hello! I need shoulders to cry on. Used to be a regular poster a few years ago, but drifted away, partly because I had to spend all my spare time studying instead of MNng.. Now I'm a newly qualified psychotherapist and DD is (possibly) a newly diagnosed epileptic. I say 'possibly' because she has only had one seizure. But children with her rare genetic syndrome seem rather prone to epilesy. We've been given emergency meds to carry at all times and an appointment with a consultant apparently within 4 weeks. I don't really want advice--just to know what it's like to live with the constant possibility of another seizure at any time...
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zzzzz ·
14/09/2016 04:18
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