Re: Help! My kid has started lisping. TMG?

[Guest guest]

Hi ,

Why not DMG instead? What are you using it for? I gave my son TMG instead

of his regular DMG for a while and he started having all sorts of behavioral

problems. I was told the difference was that TMG was a " step beyond " DMG so

it may be a " stronger " product than DMG. What ended up happening is enough

people told me that our little guy may actually need to go through the

" converting process of that step " in order for the product to benefit the child.

As I

understand it, some people have problems and need DMG and some people benefit

from TMG. http://www.autism.org/dmg.html

I think if he is having any issue what so ever that may coincide with TMG, I

would try DMG. He may be one of these kiddos who TMG has a bad effect on.

Have you noticed any positive changes?

[Guest guest]

That seems like a high dose???

Carla

[ ] Help! My kid has started lisping. TMG?

Over the past month or so, we've slowly been introducing TMG to our

son (almost 5yo, Aspergers). He's also getting B-12 shots and folinic

acid. We've noticed that coincidental with the TMG, his enunciation

seems to be changing. Most noticeable is a lisp: it started with him

pronouncing his S's like SH, but now he's sticking his tongue between

his teeth and it's coming out almost like a TH sound. It seems really

weird to think that TMG could cause a lisp. Has anyone had this

experience? The lisping started pretty early on, when he was getting

maybe 250mg/day of TMG. He's now up to 750mg/day.

-

=======================================================

[Guest guest]

Well, our DAN dr asked us to try to work it up to 8 caps/day if he

tolerated it, and we're only up to 6 caps/day so far. What do you

think is a better dose?

--- In , " Carla Pham " <carlampham@c...>

wrote:

> That seems like a high dose???

>

> Carla

> [ ] Help! My kid has started lisping. TMG?

>

>

> Over the past month or so, we've slowly been introducing TMG to

our

> son (almost 5yo, Aspergers). He's also getting B-12 shots and

folinic

> acid. We've noticed that coincidental with the TMG, his

enunciation

> seems to be changing. Most noticeable is a lisp:

[Guest guest]

,

No, I haven't noticed any improvements with the TMG. It's sort of the

story of our son's treatment that very few things we try produce any

positive change, but most things (like B6, enzymes, now possibly

TMG), if given in high enough dose, produce a negative reaction.

We are so anxious to begin chelation, which I believe will be within

the next week or two.

Thanks for the link to info on DMG. I'm going to try to research both

DMG and TMG a little more before I discuss this with my doctor next

week. Thanks for the advice.

> Hi ,

>

> Why not DMG instead? What are you using it for? I gave my son

TMG instead

> of his regular DMG for a while and he started having all sorts of

behavioral

> problems. I was told the difference was that TMG was a " step

beyond " DMG so

> it may be a " stronger " product than DMG. What ended up happening

is enough

> people told me that our little guy may actually need to go through

the

> " converting process of that step " in order for the product to

benefit the child. As I

> understand it, some people have problems and need DMG and some

people benefit

> from TMG. http://www.autism.org/dmg.html

>

> I think if he is having any issue what so ever that may coincide

with TMG, I

> would try DMG. He may be one of these kiddos who TMG has a bad

effect on.

> Have you noticed any positive changes?

>

>