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Re: Re: Is this typical?

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Debbie,

Wow... it sounds like you've tried almost every trick in the book. Too bad he

won't drink the electrolyte drink but I know you can't force him.

Is it the phenols in those foods that cause the hyper-stimminess and the red

cheeks?

What about digestive enzymes? Have you ever tried them?

I see that you're not using any nuts. Do those cause problems for him? I'm just

thinking that adding in a little pecan flour in a muffin might help with

constipation just a bit.

I'm just really uncomfortable with a kid not having a BM for several days. I'm

sure he is, too!

I seem to remember something posted on another list about magnesium citrate. I

will look for it and forward it to you privately. It could be that if you tried

another form of magnesium, you might not get that stimmy response. I know that

magnesium oxide is considered a poor form, in terms of absorbtion.... but it

does have a laxative effect, too, like the citrate. Have you tried that one?

It just sounds like you have a kid with a super-duper leaky gut.... and that's

why he reacts to so many of these foods. I sure hope we can find something that

helps.

Patti

Re: Is this typical?

Patti,

>

> Constipation is fairly common in the beginning.

> Have you tried the electrolyte drink? I keep hearing people

reporting that it helps so much with constipation.

I've tried it, but he won't drink it even when I mix his juice in

with it to make it taste better. I've also tried the constipation

protocol, but prune juice gives him horrible rashy cheeks and he gets

wild running around stimming, hyper, etc.

> Does he take the magnesium and vit C on a daily basis? Or do you

only use those in large doses when he's constipated? I was just

wondering if maybe a little bit higher daily dose would keep it from

getting so bad. You've probably already thought of that.

I think that he is reacting to the magnesium now. Every time I give

it to him he has problems at school and he seems to be more stimmy.

The vitamin C makes his bm's total liquid. That is why I don't give

these daily anymore. After 3 days of giving him these, he is hyper,

not focues, verbally stimming, visual stimming, etc. That is why we

are praying that this diet will heal his gut enough to keep him from

having this C problem so we don't have to mess him up by giving him

stuff to get him to have a bm.

> Cooked apples and ripe bananas are both.... reportedly....

considered to be " binding " . In other words, they tend to firm up the

stool... so they are good foods for someone who has diarrhea. Might

not be good in his case.

I've taken these out of his diet off and on over the past couple of

years and it doesn't seem to make a difference in causing his C, it

seems like he does better with the banana in his diet than without

it. Like I said in my earlier post, he will have a week or more of

eating these foods and having good bm's daily without any stuff to

make him go, then without a reason we can determine, he stops going.

> Do you mix any pureed veggies into his meat patties? This is one

way to hide them.

I keep trying. He is very very picky about the texture of his meat

patties, so it has been hard.

> When you say he " doesn't tolerate " zucchini, butternut squash or

pumpkin... what do you mean by that? What happens?

He gets rashy red cheeks and I see some behavior changes. The same

thing with egg yolk and lots of other foods.

Debbie

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I want to correct myself.... I just wrote:

<<magnesium oxide is considered a poor form, in terms of absorbtion.... but it

does have a laxative effect>>

I actually have always thought this was true.... but just ran across the

following info on magnesium at the Kirkman Labs website, so wanted to pass it

along:

<< Oxide- Tends to firm stools

Glycinate- A very gentle form, easier on the system

Citrate- Tends to loosen stools

Sulfate- Tends to loosen stools

Chloride- Tends to loosen stools >>

Patti

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Instead of using peanut butter in the waffles and muffins, you can try cashew

butter / almond butter. Same texture, yet much easier to tolerate.

debkirk3 wrote: Patti,

>

> Is it the phenols in those foods that cause the hyper-stimminess

and the red cheeks?

I'm not sure. The red cheeks are more like eczema, not just the

feverish red cheeks that tend to be more from phenol.

> What about digestive enzymes? Have you ever tried them?

I have the No-Fenol, but can't seem to get on a regular system for

it. I also want to start adding in other digestive enzymes. I've

just been trying to get him on a group of foods I know I can trust,

then I wanted to add them in. I think I should probably start adding

them in though and they may help him tolerate more things.

>

> I see that you're not using any nuts. Do those cause problems for

him? I'm just thinking that adding in a little pecan flour in a

muffin might help with constipation just a bit.

He does fine with pecans, hazelnuts, and macadamia nuts, but he

doesn't seem to like the nut muffins I've made. We were SCD for a

year a little over a year ago and he only liked the peanut butter

waffles or muffins I would make. I started peanut butter way too

early last time and gave him way too much, and that is why I think we

didn't do as well on SCD as we could have. I think he might like the

nut muffins if I could get some other flavor in them that would mask

some of the nutty flavor.

>

> I'm just really uncomfortable with a kid not having a BM for

several days. I'm sure he is, too!

I hate it too. Some of his behavior could be not having a bm for so

many days.

Debbie, mom to Carson 4 ASD, SCD 10/06

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It is. Try making pecan butter- 1 cup pecans with 1 Tbsp. oil-blend in fp until

smooth.

Meleah

Re: Is this typical?

>

> Instead of using peanut butter in the waffles and muffins, you can

try cashew butter / almond butter. Same texture, yet much easier to

tolerate.

>

He can't tolerate the almond butter, but I thought the cashew butter

was supposed to be used later also.

Debbie, mom to Carson 4 ASD, SCD 10/06

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