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yeast / diet

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Hello-

 

My son is 6 with PDD, " high functioning " for loss of better words.  I am trying

to figure out what type of diet to do with him.  He is now on low carbs, no

sugar, colors, etc.  He has always had high stims and can be giggly in an

inappropriate way also.  He did have +2 yeast in his stool about 1 year ago or

less. 

Being on the protocol, is it thought the yeast will get more in check with

the treatment and eating certain carbs does not really cause the troubles with

high yeast levels?  Or is the idea to really starve the body of yeast feeding

foods while on the protocol to really get it in check? 

My son has been gfcf in the past for about a year, when he went back on gluten,

there was no real notable difference in behavior, etc.  It sounds like the

diet for many works better (unless there is an allergy to gluten of course,

etc.).  It sounds like the focus is low allergy vs. gluten free?  We do millet

bread, but maybe this is worse?

Does anyone have the Do's and Dont's of the diet listed in a format they

could emial to me? 

What about Calcium supps?  It sounds like these are not necessary? 

Thanks for any help and thoughts.

Angie

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