Guest guest Posted November 4, 2008 Report Share Posted November 4, 2008 Tom used to have them and it wasn't lack of engaging because he would disappear mid-laughter/ mid-tickles/ mid-fun and at other times - it was a physical condition. We have one on video. He doesn't suffer them any more and I wish I could pinpoint which bit of biomed helped him but I can't. I imagine it was either a combination of everything or chelation, Sara candicecbt wrote: > > I used to suspect that my son might have 'petit mal' as well last > year.......and our VB therapists suggested the same because he was > not engaging!! > > After a year, he is a different child now....my conclusion is to get > him engaged in things he is interested in all the time so he has no > chance to 'stim' or gaze into space 'petit mal'! > > Be your child's playmate and do interesting things together, and > reward him for every little thing, building self esteem along the > way. A combination of RDI and play with a dash of VB principle. > > Don't rely on the ABA or VB team to do this job because the time your > child spent with you is as good as gold to them. > > > > > > Hi I was hoping that I could get some advice as I have a strong > > suspicion that Sophie is having " small " fits what used to be called > > petit mal.I used to work as a nurse in neurology many years ago so > I am > > reluctant to get into medications as I seem to remember the side > > effects often massively outweighed the benefits of the drugs...... > but > > I am wondering what people on here think as I am more inclined to > > listen carefully to people with real experience rather than my > useless > > GP.Shoul I try and get an EEG done? Although I know they can be > > inconclusive? What other approaches supps may be helpful? I would > be so > > grateful for any input emx > > > > Quote Link to comment Share on other sites More sharing options...
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