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Today is my one week aniversary on armour! I may be imagining it,

but I have not felt this good since before my thyroid was yanked. I

blew my boss away yesterday with all the things and ideas that were

busting out of my mouth.

I do have a question. How do you take your armour or other natural

thyroid? I've read that it's best to split the dose, once in the

morning and again in the afternoon. So far, I'm taking the dose in

the a.m. and seem to be doing ok.

For several years I've blamed my fatigue and other issues on this

monster I have called multiple sclerosis, but I'm beginning to think

that it's been a combo of thryoid and the MS. Since both are

autoimmune (I cant spell this morning), who knows what's what.

HAVE A GREAT DAY!!!

Lynn

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> Today is my one week aniversary on armour! I may be imagining it,

> but I have not felt this good since before my thyroid was yanked.

Hooray!! You are not imagining it. I, too, felt the difference

within one week. And I wasn't even on my optimal dose yet, which I

had to figure out over the next few months.

Like Carol said, you can figure out what works best for you with the

dosing/dividing. It is simply an attempt to more closely replicate

what your own thyroid would be doing i.e. it giving you the direct

T3 throughout the day, as needed. I take my second dose in the early

AM--got the idea from a Top Doc who said he does it so that the rise

in T3 would occur at his lowest point, around 4 pm.

But some take it all at once, too, and find it works. See what you

think.

I would, though, recommend you do the Armour sublingually instead of

swallowing it. Since it is going directly to your blood stream that

way, nearly 100% of it is used, whereas digesting it causes some of

it to be affected by contents in your stomach and then the

processing of the liver. (But again, digesting it works, but

sublingually is apparently more optimal.)

Janie :o)

p.s. Would you keep us informed as you are on Armour longer, and

find your optimal dose, as to what you notice it may be doing for

your MS symptoms??

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