Guest guest Posted May 29, 2002 Report Share Posted May 29, 2002 Hi Jeanne, Apologies again for yesterday ! Anyway , Re the gluten /casein issue . Everything I wrote I do actually believe - that your child is feeding an addiction rather than a hunger and that he will not ever extend his diet unless you challenge his craving. However I can off as unsympathetic when I am not . Quite truly my sons diet was almost exactly the same as your sons ( except he also had an excessive thirst and drank gallons of diluted apple juice each day ). Removing even one of these foods seems so scarey and if your child is underweight too ..... ( however it does speak to his craving being nothing to do with hunger and something else driving his eating habits - you don't see many overweight heroin addicts!!!). Anyway ..re chelation . It is true I have only really encountered ythis as being part of a structured biomedical response to autism where chelation is about step twelvev rather than step one - but I know the science on this is changing all the time and maybe someone is doing this now . I will happily send you details of a USA based discussion group who are all trying this - but I will do that off the board if you don't mind ( I do get criticised for trying to ensnare you unwitting innocents with my outlandish ideas and, as even I consider chelation a little radical I don't want anyone thinking they'll just give it a little try !) I would also suggest that in your circumstances you may want to check out the ARI site ( Autism Research Institute ) . It is part of the Defeat Autism Now organisation and uses specialists in this area ( such as DR Rimland ) to work out and review specific protocols for working through all biomedical intereventions for children with autism . They have a list of Doctors who understand and support the protocol and who can arrange appropriate testing etc as well as directing a regime of supplements etc for you . The site is www.autism.com ( The Doctors list is at www.autism.com/ari/danlist). I think you will be surprised that there are so many reputable , regular Doctors who are open to this , who see that the climbing figures and this new manifestation of autism/PDD have nothing to do with Kanner and everything to do with disturbed gut function. As with everything else though try and check that you are confident with any particular Doctor ( a good sound medical education does not mean that any particular practitioner has kept him/herself up to date - or is thorough , professional or even has good people skills !! And the DAN list is adjusted yearly but ....always worth checking !!). One way to do this may be to go to a discuassion board like group GFCFkids where you may find recommendations for good DAN practitioners in your area . If you want the chelation site that may also be a good place to double check for recommendations. I hope this is of some help and makes up for my curt reply yesterday !! Regards Deborah PS the small child crisis was a HUGE reaction to some gluten eaten in the form of some birthday cake on Sunday ! He is being very difficult and displaying behaviours I haven't seen for months ( looking sideways at the TV and waggling his fingers just within his peripheral vision . He is denmanding foods he hasn't had for months and this morning I am awake at 5.00 am as the diarroeha has just started .....Good morning everyone !! -- In @y..., jbmistletoe@a... wrote: > hi all, > my youngest son josh, is diagnosed with pdd. After I sent the information > about the autism article someone posted about the metals in the child's > system. > I have read from the digest that chelatin, was used to take out the metal > toxins from the child's system, do any of you know alot about and are using > this method? I am also looking in to the amino acid supplement carnosine. > Because josh's very limited diet, cheerios,cheese, yogurt, bread and butter, > peanut butter and jelly, he is very picky and won't try new things or eat > vegtables. I don't want to put him on a glutin free casin free diet, he is > only 31 pounds, afraid of any changes he will loose weight, and not eat at > all. I am seeing Dr. Agin tomorrow for a re-eval. He also has exzema and > allergies. He was on zyrtec but was asked to take him off because he is using > a topic ointment anti imflamatory for his exzema. Any imput would help. > Thanks . > jeanne buesser > president, apraxia network of bergen county > outreach coordinator of cherab > www.apraxia.cc > > > Quote Link to comment Share on other sites More sharing options...
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