kirkmans transdermal glutathione lotion

[Guest guest]

Hi..

I'm Ruth (*Ann from the gfcf diet board)

I've been a member of this group forever it seems, but I never post.

I noticed some other people are using the transdermal glutathione

lotion. I've been using it for about two months now on my son and am

loving it.

First some background..

My son is three and a half mod to high functioning Autism. He's been

gfcf since he turned two.

At the beginning of the year I chelated him myself six times. I used

ALA and Thorne Captomer. I used Andy Cutler's protocal.

I stopped doing it because by the third day my son would always have

some really bad, scary reactions. Especially when using ALA.

I wanted to wait and do it with his doctor on board.

I've since realized my son has MAJOR sulfur oxidation problems

(probably caused by the mercury)

He can't tolerate sulfites at all..MSM makes him crazy.

Anyway...I started trying the glutathione lotion and I can't believe

how well he is doing on it. I can't give it to him every day. If I do

he starts to have the negative symptoms again. But he does great

getting it every other day.

At bedtime I spritz his back down with a mixture of Epsom Salts and

purified water and then I rub the lotion into his legs and feet.

I can't get over how much he is starting to talk all of a sudden.

I realize it could be just because he is three and a half now and

it's time he naturally started talking more. But it sure is a major

coincidence then.

I was wondering...could the transdermal glutathione actually be

chelating out some of the mercury?

If it's possible...I'd much rather do it this way than go back to the

DMSA and ALA.

Anyone else having the same results with the lotion?