Re: DMG vit C and much more questions help

[Guest guest]

Hi,

Your little boy is sure getting a lot of support! Great job with the

diet!

I predict the candidase is going to supercharge the Fluconazole. We

had a huge regression for about week when we added Candex. Now we

give Candex one hour before breakfast, every day. We also have

Nystatin on board (.450 ml 3x day). Our kid was super yeasty.

Have you considered Methy-B12?

Our DAN! doc told us not to use TMG with Methy-B12.

I _highly_ recommend hard chamber HBOT.

--penumbra

>

> I have been giving my son Kirkmans DMG 1/2 cap for a few months now

and I don't see much gain at all from it. I am considering dropping it

or switching brands or trying TMG. My son is 2 years 10 months and

weighs 24 pounds (little guy!)

>  

> We have also tried vit. C as we know he really needs it in the

healing but him seems to have a sore tummy after (he is non verbal)

but he loses appetite we tried Calcium ascorbate crystals from new

roots 1/8 to 1/4 teaspoon but it doesn't seem to work for him. My son

is not a big drinker so it is hard to get him to drink the dissolved

crystals so we were putting them in the apple/pear sauce so maybe it

was too concentrated? Since joining this group I am now trying to fine

tune his supplement protocol to make sure we are getting the most out

of it.

> We have been at this for about six months and have seen a few gains

but not as much as the initial gains of changing to GFCF about one

month after the diagnoses.

> He is also taking

> digest Gold,

>  Selectra multi vitamen,

> Co Q10 kirkmans,

> Fluconazole,c

> od liver oil,(Nordic 1/2 teaspooon),

> Cal/Mag 3 caps per day (thorne)

> zinc 1/2 cap (genestra)

> P5P 1/2 cap (throne)

> custom probiotics from DD

> Omgea 3

> Flora pro liquid magnese cutom from DD 1 teaspoon /day

> L-Glutathione 250mg (douglas labs) giving rectally before bed as

sugested by our DD

> just added in vira stop and candidase

>  

> Any advice would be great

>

[Guest guest]

Thanks for the point on the TMG and Methy-B12, we have also been been giving Methy B-12 for a few months now every three days.

Thanks for the advice, penumbra

Shell

Subject: Re: DMG vit C and much more questions helpTo: mb12 valtrex Received: Friday, October 24, 2008, 2:29 AM

Hi,Your little boy is sure getting a lot of support! Great job with the diet!I predict the candidase is going to supercharge the Fluconazole. We had a huge regression for about week when we added Candex. Now we give Candex one hour before breakfast, every day. We also have Nystatin on board (.450 ml 3x day). Our kid was super yeasty.Have you considered Methy-B12?Our DAN! doc told us not to use TMG with Methy-B12. I _highly_ recommend hard chamber HBOT.--penumbra>> I have been giving my son Kirkmans DMG 1/2 cap for a few months now and I don't see much gain at all from it. I am considering dropping it or switching brands or trying TMG. My son is 2 years 10 months and weighs 24 pounds (little guy!) >

> We have also tried vit. C as we know he really needs it in the healing but him seems to have a sore tummy after (he is non verbal) but he loses appetite we tried Calcium ascorbate crystals from new roots 1/8 to 1/4 teaspoon but it doesn't seem to work for him. My son is not a big drinker so it is hard to get him to drink the dissolved crystals so we were putting them in the apple/pear sauce so maybe it was too concentrated? Since joining this group I am now trying to fine tune his supplement protocol to make sure we are getting the most out of it. > We have been at this for about six months and have seen a few gains but not as much as the initial gains of changing to GFCF about one month after the diagnoses.> He is also taking> digest Gold,> Selectra multi vitamen,> Co Q10 kirkmans, > Fluconazole, c> od liver oil,(Nordic 1/2 teaspooon),>

Cal/Mag 3 caps per day (thorne)> zinc 1/2 cap (genestra)> P5P 1/2 cap (throne)> custom probiotics from DD> Omgea 3> Flora pro liquid magnese cutom from DD 1 teaspoon /day> L-Glutathione 250mg (douglas labs) giving rectally before bed as sugested by our DD> just added in vira stop and candidase > > Any advice would be great>

[Guest guest]

Hi

My son is not much younger than yours : ) Have you tried kirkmans

vitamin c hypoalergenic buffered? Its easier on the tummy. We also had

huge gains with GF/CF. My son acts up on calcium and we found he is

high in it from his blood work. I was so worried he would be low..It sounds like

your doing great. We also use glutathione but the cream. Will your son take cod

liver oil? This was another big for us. We started DMG a few weeks ago and

didnt see anything much so I slowly upped the dose and he was more vocal

( so far 3 days ) what brand are you using?

38 and Mom to threeTasha 23..new Mommy ( means I am a Grammy )Casey-Mae 13..sweet as pieElijah 2.. ASD and beautiful

To: mb12 valtrex Sent: Thursday, October 23, 2008 10:39:57 PMSubject: Re: Re: DMG vit C and much more questions help

Thanks for the point on the TMG and Methy-B12, we have also been been giving Methy B-12 for a few months now every three days.

Thanks for the advice, penumbra

Shell

From: A Shadow <penumbraposts@ yahoo.com>Subject: Re: DMG vit C and much more questions helpTo: mb12 valtrex@ yahoogroups. comReceived: Friday, October 24, 2008, 2:29 AM

Hi,Your little boy is sure getting a lot of support! Great job with the diet!I predict the candidase is going to supercharge the Fluconazole. We had a huge regression for about week when we added Candex. Now we give Candex one hour before breakfast, every day. We also have Nystatin on board (.450 ml 3x day). Our kid was super yeasty.Have you considered Methy-B12?Our DAN! doc told us not to use TMG with Methy-B12. I _highly_ recommend hard chamber HBOT.--penumbra>> I have been giving my son Kirkmans DMG 1/2 cap for a few months now and I don't see much gain at all from it. I am considering dropping it or switching brands or trying TMG. My son is 2 years 10 months and

weighs 24 pounds (little guy!) > > We have also tried vit. C as we know he really needs it in the healing but him seems to have a sore tummy after (he is non verbal) but he loses appetite we tried Calcium ascorbate crystals from new roots 1/8 to 1/4 teaspoon but it doesn't seem to work for him. My son is not a big drinker so it is hard to get him to drink the dissolved crystals so we were putting them in the apple/pear sauce so maybe it was too concentrated? Since joining this group I am now trying to fine tune his supplement protocol to make sure we are getting the most out of it. > We have been at this for about six months and have seen a few gains but not as much as the initial gains of changing to GFCF about one month after the diagnoses.> He is also taking> digest Gold,> Selectra multi vitamen,> Co Q10 kirkmans, > Fluconazole, c>

od liver oil,(Nordic 1/2 teaspooon),> Cal/Mag 3 caps per day (thorne)> zinc 1/2 cap (genestra)> P5P 1/2 cap (throne)> custom probiotics from DD> Omgea 3> Flora pro liquid magnese cutom from DD 1 teaspoon /day> L-Glutathione 250mg (douglas labs) giving rectally before bed as sugested by our DD> just added in vira stop and candidase > > Any advice would be great>

[Guest guest]

Hi ,

I too have started DMG with my daughter and didn’t notice

much either, but have been reluctant to up the dosage. What mg are giving

daily? My daughter is 4 and 38 lbs.

Thanks in advance,

Janet

From:

mb12 valtrex [mailto:mb12 valtrex ] On Behalf

Of Largey

Sent: Thursday, October 23, 2008 8:51 PM

To: mb12 valtrex

Subject: Re: Re: DMG vit C and much more questions help

Hi

My son is not much younger

than yours : ) Have you tried kirkmans

vitamin c hypoalergenic

buffered? Its easier on the tummy. We also had

huge gains with GF/CF. My son

acts up on calcium and we found he is

high in it from his blood

work. I was so worried he would be low..It sounds like

your doing great. We also use

glutathione but the cream. Will your son take cod

liver oil? This was another

big for us. We started DMG a few weeks ago and

didnt see anything much so I

slowly upped the dose and he was more vocal

( so far 3 days ) what brand

are you using?

38 and Mom to three

Tasha 23..new Mommy ( means I am a Grammy )

Casey-Mae 13..sweet as pie

Elijah 2.. ASD and beautiful

To: mb12 valtrex

Sent: Thursday, October 23, 2008 10:39:57 PM

Subject: Re: Re: DMG vit C and much more questions help

Thanks for the point on the TMG and Methy-B12, we have

also been been giving Methy B-12 for a few months now every three days.

Thanks for the advice, penumbra

Shell

From: A Shadow

<penumbraposts@ yahoo.com>

Subject: Re: DMG vit C and much more questions help

To: mb12 valtrex@ yahoogroups. com

Received: Friday, October 24, 2008, 2:29 AM

Hi,

Your little boy is sure getting a lot of support! Great job with the

diet!

I predict the candidase is going to supercharge the Fluconazole. We

had a huge regression for about week when we added Candex. Now we

give Candex one hour before breakfast, every day. We also have

Nystatin on board (.450 ml 3x day). Our kid was super yeasty.

Have you considered Methy-B12?

Our DAN! doc told us not to use TMG with Methy-B12.

I _highly_ recommend hard chamber HBOT.

--penumbra

>

> I have been giving my son Kirkmans DMG 1/2 cap for a few months now

and I don't see much gain at all from it. I am considering dropping it

or switching brands or trying TMG. My son is 2 years 10 months and

weighs 24 pounds (little guy!)

>

> We have also tried vit. C as we know he really needs it in the

healing but him seems to have a sore tummy after (he is non verbal)

but he loses appetite we tried Calcium ascorbate crystals from new

roots 1/8 to 1/4 teaspoon but it doesn't seem to work for him. My son

is not a big drinker so it is hard to get him to drink the dissolved

crystals so we were putting them in the apple/pear sauce so maybe it

was too concentrated? Since joining this group I am now trying to fine

tune his supplement protocol to make sure we are getting the most out

of it.

> We have been at this for about six months and have seen a few gains

but not as much as the initial gains of changing to GFCF about one

month after the diagnoses.

> He is also taking

> digest Gold,

> Selectra multi vitamen,

> Co Q10 kirkmans,

> Fluconazole, c

> od liver oil,(Nordic 1/2 teaspooon),

> Cal/Mag 3 caps per day (thorne)

> zinc 1/2 cap (genestra)

> P5P 1/2 cap (throne)

> custom probiotics from DD

> Omgea 3

> Flora pro liquid magnese cutom from DD 1 teaspoon /day

> L-Glutathione 250mg (douglas labs) giving rectally before bed as

sugested by our DD

> just added in vira stop and candidase

>

> Any advice would be great

>

[Guest guest]

Hi ,

yes we are giving cod liver oil nordic naturals 1/2 teaspoon daily. The DMG we are using is Kirkmans but only 1/2 cap per day the last time I did an increase he seemed off so I went back to half a cap. Maybe it was not DMG related. My guy is small, about 24-25 pounds. I will look into kirkman hypo allergenic vitmen c.

Thanks

Shell

From: A Shadow <penumbraposts@ yahoo.com>Subject: Re: DMG vit C and much more questions helpTo: mb12 valtrex@ yahoogroups. comReceived: Friday, October 24, 2008, 2:29 AM

Hi,Your little boy is sure getting a lot of support! Great job with the diet!I predict the candidase is going to supercharge the Fluconazole. We had a huge regression for about week when we added Candex. Now we give Candex one hour before breakfast, every day. We also have Nystatin on board (.450 ml 3x day). Our kid was super yeasty.Have you considered Methy-B12?Our DAN! doc told us not to use TMG with Methy-B12. I _highly_ recommend hard chamber HBOT.--penumbra>> I have been giving my son Kirkmans DMG 1/2 cap for a few months now and I don't see much gain at all from it. I am considering dropping it or switching brands or trying TMG. My son is 2 years 10 months and weighs 24 pounds (little guy!) >

> We have also tried vit. C as we know he really needs it in the healing but him seems to have a sore tummy after (he is non verbal) but he loses appetite we tried Calcium ascorbate crystals from new roots 1/8 to 1/4 teaspoon but it doesn't seem to work for him. My son is not a big drinker so it is hard to get him to drink the dissolved crystals so we were putting them in the apple/pear sauce so maybe it was too concentrated? Since joining this group I am now trying to fine tune his supplement protocol to make sure we are getting the most out of it. > We have been at this for about six months and have seen a few gains but not as much as the initial gains of changing to GFCF about one month after the diagnoses.> He is also taking> digest Gold,> Selectra multi vitamen,> Co Q10 kirkmans, > Fluconazole, c> od liver oil,(Nordic 1/2 teaspooon),>

Cal/Mag 3 caps per day (thorne)> zinc 1/2 cap (genestra)> P5P 1/2 cap (throne)> custom probiotics from DD> Omgea 3> Flora pro liquid magnese cutom from DD 1 teaspoon /day> L-Glutathione 250mg (douglas labs) giving rectally before bed as sugested by our DD> just added in vira stop and candidase > > Any advice would be great>

[Guest guest]

To - When you say you upped the dose of DMG;

Please reveal to us-- What amount are you giving?

" Verizon " wrote:

Hi ,

I too have started DMG with my daughter and didn't notice much

either, but have been reluctant to up the dosage. What mg are giving

daily? My daughter is 4 and 38 lbs.

Thanks in advance,

Janet

On Behalf Of Largey>>>

Hi

> My son is not much younger than yours : ) Have you tried kirkmans

>vitamin c hypoalergenic buffered? Its easier on the tummy. We also

had huge gains with GF/CF. My son acts up on calcium and we found he

is high in it from his blood work. I was so worried he would be

low..It sounds like your doing great. We also use glutathione but the

cream. Will your son take cod liver oil? This was another big for us.

We started DMG a few weeks ago and didnt see anything much so I

slowly upped the dose and he was more vocal( so far 3 days ) what

brand are you using?

>

>

> 38 and Mom to three

> Tasha 23..new Mommy ( means I am a Grammy )

> Casey-Mae 13..sweet as pie

> Elijah 2.. ASD and beautiful

[Guest guest]

Hi

I think with DMG, being its a methyl donor, some kids react negatively

if they are over methylaters..Just like with Mb12. How long ago did you start

your little guy on mb12? If it wasnt that long ago, it might be just that he

is still adjusting to better methylation? Just a thought.

The first few times I gave my son DMG he either got a tiny bit hyper or it

didnt seem to do anything. Then I read some kids need small doses through

out the day. I use Food Science of Vermont liquid which we really like. It is pricey

but 1 ml is 300 mg. I bought it thinking if it didnt work, I could use it. Its great for

the immune system. So I have been giving 100mg in the am, noon, and again

at like 4 pm. I am also thinking next time trying this product to add

http://www.fslabs.com/vitamins-supplements/behavior-balance-dmg.php

... buffered c was much better tolerated by my little guy. Worth a shot

vitamin c is such a good supplement : )

38 and Mom to threeTasha 23..new Mommy ( means I am a Grammy )Casey-Mae 13..sweet as pieElijah 2.. ASD and beautiful

To: mb12 valtrex Sent: Friday, October 24, 2008 7:24:27 AMSubject: Re: DMG vit C and much more questions help

To - When you say you upped the dose of DMG; Please reveal to us-- What amount are you giving?"Verizon" <micklane333@ ...> wrote:Hi ,I too have started DMG with my daughter and didn't notice much either, but have been reluctant to up the dosage. What mg are giving daily? My daughter is 4 and 38 lbs. Thanks in advance,JanetOn Behalf Of Largey>>>Hi > My son is not much younger than yours : ) Have you tried kirkmans>vitamin c hypoalergenic buffered? Its easier on the tummy. We also had huge gains with GF/CF. My son acts up on calcium and we found he is high in it from his blood work. I was so worried he would be low..It sounds like your doing great. We also use glutathione but the cream. Will your son take cod liver oil? This was another big for us. We started DMG a few weeks ago and didnt see anything much so I slowly upped the

dose and he was more vocal( so far 3 days ) what brand are you using?> > > 38 and Mom to three> Tasha 23..new Mommy ( means I am a Grammy )> Casey-Mae 13..sweet as pie> Elijah 2.. ASD and beautiful

[Guest guest]

Sorry I forgot to add my son is 30 lbs..after being 28 lbs

for almost a year 38 and Mom to threeTasha 23..new Mommy ( means I am a Grammy )Casey-Mae 13..sweet as pieElijah 2.. ASD and beautiful

To: mb12 valtrex Sent: Friday, October 24, 2008 7:24:27 AMSubject: Re: DMG vit C and much more questions help

To - When you say you upped the dose of DMG; Please reveal to us-- What amount are you giving?"Verizon" <micklane333@ ...> wrote:Hi ,I too have started DMG with my daughter and didn't notice much either, but have been reluctant to up the dosage. What mg are giving daily? My daughter is 4 and 38 lbs. Thanks in advance,JanetOn Behalf Of Largey>>>Hi > My son is not much younger than yours : ) Have you tried kirkmans>vitamin c hypoalergenic buffered? Its easier on the tummy. We also had huge gains with GF/CF. My son acts up on calcium and we found he is high in it from his blood work. I was so worried he would be low..It sounds like your doing great. We also use glutathione but the cream. Will your son take cod liver oil? This was another big for us. We started DMG a few weeks ago and didnt see anything much so I slowly upped the

dose and he was more vocal( so far 3 days ) what brand are you using?> > > 38 and Mom to three> Tasha 23..new Mommy ( means I am a Grammy )> Casey-Mae 13..sweet as pie> Elijah 2.. ASD and beautiful

[Guest guest]

about the vitamin c he might be developing oxalates from it. it can

happen when you have a leaky gut. I too was doing high doses of vit.

C and my kid would start flapping and he was obviously in a lot of

pain. I dropped it and went on a low oxalate diet for a while and

that helped tremendously to dump excess oxalate.

> >

> > I have been giving my son Kirkmans DMG 1/2 cap for a few months

now

> and I don't see much gain at all from it. I am considering dropping

it

> or switching brands or trying TMG. My son is 2 years 10 months and

> weighs 24 pounds (little guy!)

> >  

> > We have also tried vit. C as we know he really needs it in the

> healing but him seems to have a sore tummy after (he is non verbal)

> but he loses appetite we tried Calcium ascorbate crystals from new

> roots 1/8 to 1/4 teaspoon but it doesn't seem to work for him. My

son

> is not a big drinker so it is hard to get him to drink the

dissolved

> crystals so we were putting them in the apple/pear sauce so maybe

it

> was too concentrated? Since joining this group I am now trying to

fine

> tune his supplement protocol to make sure we are getting the most

out

> of it.

> > We have been at this for about six months and have seen a few

gains

> but not as much as the initial gains of changing to GFCF about one

> month after the diagnoses.

> > He is also taking

> > digest Gold,

> >  Selectra multi vitamen,

> > Co Q10 kirkmans,

> > Fluconazole,c

> > od liver oil,(Nordic 1/2 teaspooon),

> > Cal/Mag 3 caps per day (thorne)

> > zinc 1/2 cap (genestra)

> > P5P 1/2 cap (throne)

> > custom probiotics from DD

> > Omgea 3

> > Flora pro liquid magnese cutom from DD 1 teaspoon /day

> > L-Glutathione 250mg (douglas labs) giving rectally before bed as

> sugested by our DD

> > just added in vira stop and candidase

> >  

> > Any advice would be great

> >

>