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HI MY NAME IS VICKI LOWERY AND I AM INTRESTED IN KNOWING WHAT TMG IS AND HOW

IT IS GIVEN TO THE CHILD??(PILL FORM OR LIQUID) AND WHAT SUPPLEMENTS DO YOU

RECOMMEND FOR CHILDREN LIKE MY SON WHO IS ONLY 5 AND CANT SWALLOW PILLS YET.

THANKS

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In the Summer of 2000, I had read about DMG helping some autistic kids. So,

I started na on it and saw some improvements, the improvements were

slow, but there. More eye contact and she started recognizing her father. I

upped the dose a little and saw a little more. This went on until she was

getting 5 125mg a day, there was no further improvement by giving her 6. I

was reluctant to try taking her off of it, but there came a time when we ran

out and would be unable to get more for a few days (the closest town that

had it is 40 min. away and we just couldn't get there). There were no

regressions. She was on it for a year and has been off of it for 6 months.

Since then I have been hearing of TMG. What is the difference? And did

anyone start their kid on DMG then switch to TMG and get better results?

Does it also need to be accompanied by other B vitamins? I appreciate any

input from anyone using TMG.

Thanks,

Tana

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Hi Tana,

DMG was the first thing which helped to my son (3 years old).

I saw improvements almost immediately, he became more active and

interested in the world. I noticed this progress as soon as I started

DMG, and I had him for 3 months on DMG. He performed on the same

level which he reached in first several days. After that I switched

to TMG. The result was very impressive, and I could see it

immediately. His eye contact became just normal, stereotyped

behaviors diminished greatly and some of them disappeared, and

instead of running and lying on the floor he started playing with

toys. Teeth grinding disappeared. I had TMG without B12 and folic

acid, and several nights after that could not sleep. He was

very happy and still wanted to play and investigate the world at

night, but I was very tired. I ordered TMG with B12 and folic acid,

and we started sleeping during the night again. Performance was a

little bit worse. I tried to switch several times between

preparations with b12 and folic acid and without them, it seems that

he performs a little bit better on pure TMG formula but every time we

have sleepless night on it.

I am very interested to hear about other kids who improved with TMG

or DMG. It shows to some type of biochemistry. What other treatments

did help?

Margaret

> In the Summer of 2000, I had read about DMG helping some autistic

kids. So,

> I started na on it and saw some improvements, the improvements

were

> slow, but there. More eye contact and she started recognizing her

father. I

> upped the dose a little and saw a little more. This went on until

she was

> getting 5 125mg a day, there was no further improvement by giving

her 6. I

> was reluctant to try taking her off of it, but there came a time

when we ran

> out and would be unable to get more for a few days (the closest

town that

> had it is 40 min. away and we just couldn't get there). There were

no

> regressions. She was on it for a year and has been off of it for 6

months.

> Since then I have been hearing of TMG. What is the difference? And

did

> anyone start their kid on DMG then switch to TMG and get better

results?

> Does it also need to be accompanied by other B vitamins? I

appreciate any

> input from anyone using TMG.

>

> Thanks,

> Tana

>

>

>

>

>

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Some chemical information but no practical experience:

TMG is DMG with another methyl group stuck on the nitrogen.

TMG is thought of more as a methyl source, which helps vitamins B-12

and folic acid do their things. However, once the methyl group comes

off it IS DMG.

Andy

> In the Summer of 2000, I had read about DMG helping some autistic

kids. So,

> I started na on it and saw some improvements, the improvements

were

> slow, but there. More eye contact and she started recognizing her

father. I

> upped the dose a little and saw a little more. This went on until

she was

> getting 5 125mg a day, there was no further improvement by giving

her 6. I

> was reluctant to try taking her off of it, but there came a time

when we ran

> out and would be unable to get more for a few days (the closest town

that

> had it is 40 min. away and we just couldn't get there). There were

no

> regressions. She was on it for a year and has been off of it for 6

months.

> Since then I have been hearing of TMG. What is the difference? And

did

> anyone start their kid on DMG then switch to TMG and get better

results?

> Does it also need to be accompanied by other B vitamins? I

appreciate any

> input from anyone using TMG.

>

> Thanks,

> Tana

>

>

>

>

> [Non-text portions of this message have

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I buy TMG from Kirkman Labs http://www.kirkmanlabs.com . They have it

in liquid, powder and capsules. You can try liquid or powder (my son

swallows capsules - I put them inside banana)

Margaret

> HI MY NAME IS VICKI LOWERY AND I AM INTRESTED IN KNOWING WHAT TMG

IS AND HOW

> IT IS GIVEN TO THE CHILD??(PILL FORM OR LIQUID) AND WHAT

SUPPLEMENTS DO YOU

> RECOMMEND FOR CHILDREN LIKE MY SON WHO IS ONLY 5 AND CANT SWALLOW

PILLS YET.

> THANKS

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Hi Tana, TMG is the " big brother " of DMG and is stronger. Given for the

samer reasons, it is linked to helping make gains in speech. Come is liquid

from Kirkmans, nice flavor, you start 1/2 t twice a day and build up to a

teaspoon twice a day. My son has been on it 3 months as we are slowely

moving up to 2 teaspoons twice a day. You move slow because it can make them

stimmy or hyper if you move to fast. I am not sure if it has helped or

not, simply becuase he has been improving steadly all along. I never saw

anything with DMG, however, and that is why we are trying this. :) cab

[ ] TMG & DMG

> In the Summer of 2000, I had read about DMG helping some autistic kids.

So,

> I started na on it and saw some improvements, the improvements were

> slow, but there. More eye contact and she started recognizing her father.

I

> upped the dose a little and saw a little more. This went on until she was

> getting 5 125mg a day, there was no further improvement by giving her 6. I

> was reluctant to try taking her off of it, but there came a time when we

ran

> out and would be unable to get more for a few days (the closest town that

> had it is 40 min. away and we just couldn't get there). There were no

> regressions. She was on it for a year and has been off of it for 6 months.

> Since then I have been hearing of TMG. What is the difference? And did

> anyone start their kid on DMG then switch to TMG and get better results?

> Does it also need to be accompanied by other B vitamins? I appreciate any

> input from anyone using TMG.

>

> Thanks,

> Tana

>

>

>

>

>

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I used dmg for a while with my boys. I saw alot of improvements. When I heard

of Tmg, I read up on it. It is the same as dmg, but with one more methyl

group. It produces seratonin and naturally produces SAMe. I made the switch

and I've seen even more improvements, especially in behavior, than I did with

the dmg. I did notice that there was some hyperactivity, but when I added two

800mcg of folic acid with the tmg dose, it took care of that. Hope this

helped. You can learn more about it at the kirkman labs website. They have

some interresting articles on different products for autism.

www.kirkmanlabs.com. God bless, Sharon

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Hi Sharon,

It looks like my boy has something common with your boys. Could you

please tell me what other supplements and treatments helped to your

boys?

Thank you,

Margaret

> I used dmg for a while with my boys. I saw alot of improvements.

When I heard

> of Tmg, I read up on it. It is the same as dmg, but with one more

methyl

> group. It produces seratonin and naturally produces SAMe. I made

the switch

> and I've seen even more improvements, especially in behavior, than

I did with

> the dmg. I did notice that there was some hyperactivity, but when I

added two

> 800mcg of folic acid with the tmg dose, it took care of that. Hope

this

> helped. You can learn more about it at the kirkman labs website.

They have

> some interresting articles on different products for autism.

> www.kirkmanlabs.com. God bless, Sharon

>

>

>

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After several months without liquid TMG, I put my son on the capsules

w/ folic acid & B12. He had changed schools and was a bit stressed

with new schedules, etc. So was I! We are both calmer & more

focussed after 3-5 days (faster for him than me). TMG has a number

of great properties in addition to increased SAMe, such as protection

from myelin destructive antibodies. There are good articles at

kirkmanlab.com and vrp.com, as well as other sources.

Some kids need extra folic acid to convert the TMG and will be hyper

without extra supplementation.

Some adults (count me in) find TMG very helpful in reducing the

effects of stress.

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