Guest guest Posted September 3, 2009 Report Share Posted September 3, 2009 Please help me recover my daughter joanna. She is very hard to live with ..Dunping stuff cereal,medicine anything not locked up .Puts non food items in mouth. Defiant behavior . " Look I'm on the table. " It is not a -----. " She has to say the opposite of whatever. OR what she says makes absulutely no sense. " The fire hydrandant does not fit in the Buick. " She says meaningless stuff that is not even true . Can not play. Bites. Does whatever she can to annoy. The behaviorist say to ignore bad and praise good. Much of what she does is destuctive or hurtful that is hard to annoy . When I sit to play with her she will get up and walk away. Or else like the other day sitting in my lap playing legos out of the blue " I'm going to bite you. " Eats all art activities glue ,paint.crayons shaving cream within 30 seconds after I bring them out.About three out of six of the family are starting to hate her.My teenage daughters get mad because if they leave dedorant out, shampoo, a water cup ,makeup, it gets purposely dumped. I am honestly fearful she is going to have to be institutionalized as she gets older. It is hard because every once in a blue moon she wakes up and says something rational like " You not get rid of Me? She heard the institution talk.But most of the time she is so naughty or just out of it . The regional center said her IQ is 59 with autism but two young to tell,But I swear when it comes to tormenting me her IQ jumps to 100. Her whole brain is how can I torture you? I'm kicking you.I spill the lotion. She was so smart before when she was young first word four months -just heart breaking. Says she shakes things because she has autism. But more than half the time language is echolalic except for NOT. I might say Look at the tree. Not a tree.Not, Can't ,don' t, favorite words. The car is NOT red.Help! Anything to make her more peaceful less defiant. Last night it was lotion dumped while running over large areas of carpet and my bed before I could catch her. Today was Milk of Magnesia on carpet and someone elses bed. Well Thanks for listening. From: tmykland <tmyklandprofile@...> Subject: Re: P5P Date: Wednesday, September 2, 2009, 8:41 AM P5P is kind of the " rocket fuel " form of vitamin B6, it's the active form, so it is equivalent to giving 3-5 times as much of the other form, pyridoxine, and some kids kind of bounce off the walls when starting it. It's very useful, though, so don't give up. I do not think that the below guideline is useful (i.e. 25 mg/day if phenol/sulfur problems). From what I've seen, most kids can benefit from it, but some need to start at very low doses. What you are seeing is what people often see when kids take more p5p than they can use. Here's what I would suggest: 1. Stop the p5p 2. Introduce the magnesium, which can help to counteract the excitatory effects of the p5p 3. Start p5p again, at 1/4 dose, then increase gradually, giving the body a chance to get used to it over a week or two. You can add a little B6 too, and play with doses to find out what works. p5p and B6 are two different forms of the same vitamin. Hope this is helpful. Terri btw, in case you're wondering, I have a 16yo son with autism who has taken p5p since age 3, and I work for BrainChild Nutritionals, so that's how I learned a lot about vitamins. > > > > Has anyone seen any adverse effects from giving P5P? We're supposed to introduce P5P, then magnesium glycinate, then B6. But on giving the P5P, we've noticed increased spaciness, crankiness, and vocal stims. So, not sure if we should proceed to introduce the other supps and hope they balance each other out; or stop the P5P. Would appreciate any comments, > > > > Daisy > > > Quote Link to comment Share on other sites More sharing options...
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