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In my mind, the symptoms of one side of the body being weaker and one eye being

closed

more is enough reason to do a Valtrex trial.

You and your husband may want to try an antifungal and MB12 to see if they help

him,

odds are they will. An antifungal will make you feel yucky for a couple of

days, but there

after can be a wonderful experience. I also strongly suggest acidopholus. I

use Intestinal

Care DF from whole foods. It's wonderful and I get a lot of energy from it.

You should

expect a couple of yucky days on that as well followed by energetic gains...

about 20% of

people who take acidophilus and do the diet for the first time will kick up a

nasty viral

infection that is probably mobilized from the gut. If it's there, it's an

important process.

I suggest to parents all the time that they try everything they give to their

child. It's how I

found out how great MB12 is for ADHD and IBS. Back then I took one shot and I

was

totally sold on MB12.

The issue with the tongue is fungus. It is so important to address it since it

probably

origionated in the ileum and traveled 20 feet to end up on the tongue. Fungus

also

dumps sugar, toxins, and forments alcohol along with disaccrites and

polysaccrites (or

just plain sugars).

Fungus, in of itself, can cause autism in some children and chronic fatigue in

adults.

Typically, our kids are on antifungals for months sometimes years at a time

until their

immune system catches up. In my son's case, he was on diflulcan and Valtrex for

9

months. You can see the before and after pictures of his tongue on our videos

website,

www.recoveryvideos.com His video is called Ethan's recovery, short version.

I also have some pictures of " The tongues of the chronically ill " located at:

www.childrenscornerschool.com/tongues.htm

I would start by removing grains, starches, and complex carbs along with milk

and wheat

and then try MB12 for the entire family.

I know you're just getting up to speed.

Keep us posted.

- Stan

> >

> > Hi there,

> > I'm new to the list. We are currently only doing supplements and

> MB12 injections for our son. (5 yr old) He is a real gut kid and

> was scoped by Dr. Buie when he was 2 and found to have Lymphoid

> Nodular Hyperplasia - however he never got his MMR - go figure. I

> just the preliminiary testing that Dr. Krigsman requires. Amongst

> what seemed like 10000 stool tests (maybe 12) and many tubes of

> blood, he had a KUB test which was an Xray of the tummy. Not quite

> sure what this test is actually looking for. Hope this helps.

> > ann

> >

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