Guest guest Posted May 2, 2006 Report Share Posted May 2, 2006 Not Andy, but... I say you got lucky. Congratulations! I would not attempt that again, though. Pam > > i am curious to your thoughts on my sons experience with ALA... we > were giving him ALA as a supplement 6 years ago not knowing that it > was a chelator. he got it 2 times per day for about a year everyday > which i know is not your protocal and could be dangerous somehow but > this boy is mostly recovered after that year. what are your thoughts > to this method and how it could have helped him recover? i have had > a few emails with dana and her son is doing/did well with the > protocal you support but he is not recovered!!! of course case by > case differs but at this point i can not attribute it to anything > else as we also did all the same supplements minerals and enzymes > similiar as per her web page. mostly recovered is he does not have > any of the difficulties that he had when he was on the spectrum, in > fact his dev.ped. last week confirmed he was still progressing and > has not slid back whatso ever and our hardships are only in fine > motor. his neurologist also was head of childrens hospital in canada > has never seen such improvements and is joyed to see our boy > everytime keeping pace with everything, even in speech he is fine > though articulation for4 syllable words is still a bit of a struggle > but so does his nt cousin struggle at the exact same age. (he was > extreme apraxic)im just wanting your opinion as we are about to > start chelation with our other son and want the same success for him > too!!! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2006 Report Share Posted May 2, 2006 Congratulations, I am curious how much were you giving him on a daily basis and how old was he? Good luck with your other child. (Ian's mom) [ ] question for andy??? >i am curious to your thoughts on my sons experience with ALA... we > were giving him ALA as a supplement 6 years ago not knowing that it > was a chelator. he got it 2 times per day for about a year everyday > which i know is not your protocal and could be dangerous somehow but > this boy is mostly recovered after that year. what are your thoughts > to this method and how it could have helped him recover? i have had > a few emails with dana and her son is doing/did well with the > protocal you support but he is not recovered!!! of course case by > case differs but at this point i can not attribute it to anything > else as we also did all the same supplements minerals and enzymes > similiar as per her web page. mostly recovered is he does not have > any of the difficulties that he had when he was on the spectrum, in > fact his dev.ped. last week confirmed he was still progressing and > has not slid back whatso ever and our hardships are only in fine > motor. his neurologist also was head of childrens hospital in canada > has never seen such improvements and is joyed to see our boy > everytime keeping pace with everything, even in speech he is fine > though articulation for4 syllable words is still a bit of a struggle > but so does his nt cousin struggle at the exact same age. (he was > extreme apraxic)im just wanting your opinion as we are about to > start chelation with our other son and want the same success for him > too!!! > > > > > > > ======================================================= > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2006 Report Share Posted May 2, 2006 FWIW Dana does not use Andy's protocol. I would recommend Andy's protocol for your other son. S S <BR> ><BR> > i am curious to your thoughts on my sons experience with ALA... we <BR> > were giving him ALA as a supplement 6 years ago not knowing that <BR> it <BR> > was a chelator. he got it 2 times per day for about a year <BR> everyday <BR> > which i know is not your protocal and could be dangerous somehow <BR> but <BR> > this boy is mostly recovered after that year. what are your <BR> thoughts <BR> > to this method and how it could have helped him recover? i have <BR> had <BR> > a few emails with dana and her son is doing/did well with the <BR> > protocal you support but he is not recovered!!! of course case by <BR> > case differs but at this point i can not attribute it to anything <BR> > else as we also did all the same supplements minerals and enzymes <BR> > similiar as per her web page. mostly recovered is he does not have <BR> > any of the difficulties that he had when he was on the spectrum, <BR> in <BR> > fact his dev.ped. last week confirmed he was still progressing and <BR> > has not slid back whatso ever and our hardships are only in fine <BR> > motor. his neurologist also was head of childrens hospital in <BR> canada <BR> > has never seen such improvements and is joyed to see our boy <BR> > everytime keeping pace with everything, even in speech he is fine <BR> > though articulation for4 syllable words is still a bit of a <BR> struggle <BR> > but so does his nt cousin struggle at the exact same age. (he was <BR> > extreme apraxic)im just wanting your opinion as we are about to <BR> > start chelation with our other son and want the same success for <BR> him <BR> > too!!!<BR> _______________________________________________ Join Excite! - http://www.excite.com The most personalized portal on the Web! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 >>he got it 2 times per day for about a year everyday > which i know is not your protocal and could be dangerous somehow but > this boy is mostly recovered after that year. I gave ALA 3x per day, and it was very helpful. It caused my son to lose all his food and supplement intolerances, and eliminated gut yeast [altho brain yeast is still a problem as viruses are eliminated]. > a few emails with dana and her son is doing/did well with the > protocal you support but he is not recovered!!! My son needed much more than chelation for recovery. Chelation was actually the FIRST step. It was mostly the supplements he tolerated once he was chelated, that have caused the recovery. Now he no longer qualifies as autistic, altho he is still delayed in language. I did not use Andy's protocol, I gave ALA 3x per day. >>his neurologist also was head of childrens hospital in canada > has never seen such improvements and is joyed to see our boy > everytime keeping pace with everything, even in speech he is fine Sounds great! Your child might be like mine, in that it was mostly the supplements that recovered him. Dana Quote Link to comment Share on other sites More sharing options...
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