Guest guest Posted June 14, 2011 Report Share Posted June 14, 2011 Heidi, I am not an expert in KPU, but having myself and my son treated for KPU (my son has been on the KPU protocol for the past 10 months and me only for the past 2 months) here is what I know: Some of the symptoms that both me and my son had were: inner tension, poor stress control (I was crying very easily and from being in good mood I could go into extremely sad just from small things, something that before I though it is from having a child with special needs, but now treating myself for KPU I see how I can control my mood much easier), pale skin that easily burns, eyes that are sensitive to light, white marks on our nails, tire easily, anemic, poor dream recall, poor breakfast appetite, upper abdominal pain when stressed (I still have that although not as bad as few months ago). I never had the rage episodes, thanks God, but my son had the sudden extreme frustration – he could be in a very good mood and if something small didn't go his way he would bite very hard his wrist or my wrist or whoever else was in front of him(few times until blood came out). So I definitely think that aggression is a red flag for KPU, although it is not a must, as in my case I didn't have it but I had most of the other symptoms. KPU is either given from mother to child (as it is probably in my case) or from extreme stress. The treatment in our case is high doses of the CORE supplement , which has all the necessary ingredient to address the deficits of Vitamin B-6 , Zinc ,Manganese , Chromium, Molybdenum, Boron and L-Taurine and in addition you take some form of Omegas supplement. I haven't noticed that my son was more angry from eating potatoes in the past, but he eats only red potatoes (they are the only ones allowed in the low oxalates diet), so may be that's why. The test for KPU is either with ART testing or Vitamin Diagnostics and there is usually special instructions from Dr. K how to do the test (he says to ignore Vitamin Diagnostics instructions and follow only his). About your question if anybody has resolved already his child KPU – in our case I don't consider my son's KPU problem resolved because he is still on high doses CORE supplement. However his symptoms are greatly reduced to some almost completely gone – his skin is not pale anymore, he is not anemic, no sensitivity to light, no rage episodes at all. The other symptoms is difficult to say if they are gone (like upper abdominal pain when stressed), because he is non-verbal so he doesn't tell me when something hurts, but he doesn't hold his tummy as he used to, so this makes me think that he feels better overall. Hope this helps, Krassi > > I want to get some updated information on KPU. > > 1. What can you all tell me about KPU? > > 2. Does your child with KPU have strong smells from the skin that come and go? > > 3. Has anyone resolved their child's KPU and how? > > 4. What do you think KPU issues are from? > > 5. What are some treatments/diets for it? > > 6. What are the going tests/testing procedures for it? > > 7. Do you think it's behind aggression? > > 8. Does your child with KPU get very angry after eating potatoes and other phenyl. foods? > > Love and prayers, > > Heidi N > Quote Link to comment Share on other sites More sharing options...
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