Guest guest Posted April 21, 2001 Report Share Posted April 21, 2001 I want to start by saying that I recognize that all children are different, and that the only data we have is our own little Taryn. What we have encountered may be specific to our case. After 3 months of GFCF, Taryn is now transitioning to a diet that is aimed at " eating as our grandparents did " , which includes avoiding preserved and pre-packaged foods. This includes a full glass of cow's milk and plenty of bread with each meal, and absolutely NO soy products! We are working with a semi-local organization who take a different approach to biological issues related to autism. Right now, the options are two-fold: remove the offending item from the patient's environment, or introduce a chemical to minimize the patient's reaction to the offending component. This group adds a third option: isolate the biochemical deficiency that is responsible for the atypical reaction, and introduce the appropriate enzymes, electrolytes, and other catalysts necessary to enable the person to effectively process foods. Their focus is on the entire body chemistry - both short AND long term. Ironically, the long-term physiological hazards of GF/CF began to stack up against the present neurological hazards of food-based opioids. So Taryn is now off GF/CF and Cod Liver Oil (they are concerned about Vitamin A shutting down the body's natural desire for Vitamin A-based foods). As a matter of fact, we have a full sealed, unopened bottle of Kirkman Labs CLO and jar of Enzym-Aid that we are looking to get rid of. She ran into a few regressions early on, but made a pretty surprising rebound in fairly short order. We are continuing to make constant biochemical adjustments, modifying the diet to optimize appropriate nutrients and introducing the necessary adjunct catalysts. At the same time we are working with a neurodevelopmentalist to develop a set of exercises aimed specifically at developing neurological input processing functions. This is sort of a hybrid between ABA and sensory integration. We have seen such phenomenal progress with everything that Taryn has been rediagnosed. In January, she was diagnosed as " moderately autistic. " This past week she was reclassified as " sensory integration deficient with speech development delay. " Her eye contact is incredibly high, she can't get enough hugs and cuddles from her mommy and me, she wants to play with her sister, and she shows incremental development almost daily. Best of all, we were able to give her real macaroni and cheese for dinner...her favorite before the GF/CF. Once again, I want to be sure to reinforce that I know that what I am posing here flies in the face of most everything on this list. I am forever grateful to all here who set us along the proper path, because we were able to prove definitively and conclusively that Taryn's developmental issues were predominantly based in metabolism. For many of you, undertaking GF/CF was a leap of faith. I read many stories in which many here were encountered by cynical - even hostile - family, friends and cohorts. We have undertaken a similar leap of faith and have found the payoff worth the risk. Again, it may not be the answer for others. Selfishly, I am thankful it is at least for Taryn. If as you read this you find that you would like to know more, we would be happy to share details. It is not our intention to detract from the mission of this list, which is to serve parents and guardians who wish to implement GF-CF as a means of treating their children's autism. We simply want to share with others the joys of an amazing, almost stunning ascent toward near-normalcy after such a dizzyingly short period of time. We will not be lurking around this list much longer. If you would like a response here, we will be happy to do so. If you would like a personal response, please contact us at dgstevens@... . God bless all of you as you shoulder the burden of this most unwelcome yoke. You are all in our prayers. Tim & s Parents to Kiera (6, NT) and Taryn (2-1/2, " other " ) Quote Link to comment Share on other sites More sharing options...
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