Guest guest Posted November 4, 2008 Report Share Posted November 4, 2008 Okay, friends, I am willing to let my dd be the guinea pig for the glutathione patches if one of the distributors is willing to sell them to me for the distributor price. I watched all the discussions expressing doubt about the patches because all the people who are raving about them are distributors. I understand the skepticism. However, I also understand becoming a distributor for what turns out to be $5 in order to do a longer-term trial of them. That is what I will do if I cannot get a distributor to sell them for the distributor price for three months. Every dollar counts. But for the sake of the list and everyone's curiosity, I would like to try them without becoming a distributor who would seem to have a vested interest. Here's the deal though - the child who will be officially testing them is not autistic. My autistic ds has done one blood draw and it was the worst nightmare ever. His glutathione levels were fine, so I will not do a follow up blood draw on him just to prove a point for other people, even if I do try the patches on him I won't use him as a guinea pig - he's too ill in my opinion. I also can't guarantee that I won't be doing other new interventions in that time period. I have four dc and all of them are celiac/gluten enteropathic (along with both my dh and I.) Because of that, we have been doing follow up testing to check for nutritional deficiencies and such. My 13 yo dd did the Spectracell test and she did show up as deficient in glutathione (along with other deficiencies.) We need to supplement for her. Our doctor has recommended cream, but we are willing to try the patches alone for three months to see if it raises her glutathione levels. She will be cooperative with wearing them and will be cooperative with the follow-up blood draw. I am skeptical that they will work, but I am not completely closed-minded. I am willing to risk her not raising her glutathione levels for three months because she is not showing any overt signs of a problem and she is not autistic. I don't think it will harm her terribly to wait three months if the patches don't work. If those of you on the list are interested in having me do this and if a distributor is comfortable reselling the patches to me at their cost (can you even do that? I don't want to do anything unethical) or if the company itself wants to sell it to me at the lower cost - whatever works out - I will do it this way. If not, then I will just become a distributor to get the patches for less because I do want to try them. I have never in my life participated in any sort of pyramid company and pretty much hate them, but I need to save money where I can. A family of six (one of whom is autistic) on special diets and varying supplements is unbelievably expensive. If we decide to do this, I will list everything she is currently doing regarding diet and supplements, plus her deficiencies and the exact number of her glutithione deficiency. Let me know what you all think. Blessings, Quote Link to comment Share on other sites More sharing options...
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