Re: Group Meeting Results/DAN Info.

[Guest guest]

Hey Liz,

Dont worry. You are moving in the right direction and that is all that

matters. I just went to get my daughters ears rechecked and they are fine -

Thank goodness. So I also took Charlie and he had had what looks like a zit

or boil on the outside of the beginning of his inner ear. He can now tell me

boo boo in ear thank good ness, so I took him. Of course they gave me an

antiboitic and drops. I am going to give him the drops first to see if that

does anything then if I have to give him the antiboitic, then I will get a

probiotic from my dan that can out live anitboitics. I will also call DAN!

because perhaps it is from the detox stuff.

I went back in the files and today ordered all of the tests on apraxia. Some

I have done and need to be retested. But with the results of the metal

testing coming soon and these testing we are on our way to an even more

taylor made version of therapy.

My MD is very interested in seeing Charlie's vitamin protocol. Impressed

with what is happening with Charlie. Pretty openminded guy, but like

Janice's MD from her story. Mine was much like hers, he said literally, " I

plead ignorance on this...Its a shame studies are not being conducted. " All

in all a good doc who shows interest.

Colleen

Mother of Charlie 30 months

[ ] Group Meeting Results/DAN Info.

Went to the group meeting in my town tonight. My town is 1/4 square

mile, Mayberry, everyone knows everyone elses beeswax so we signed

confidentiality agreements but are allowed to do what I am doing now

so long as we say, " Someone in my group. "

The group is made up of parents of the following types of kids but

not all have just speech issues and one, the only one exposed to

fluoride in large doses, is diagnosed with dyspraxia.

1) PDD Nos, sensory issues pretty severe.

2) Nonverbal, PDD Nos, older sibling possible Aspergers. Going to

Neubrander, slightly leary about him.

3) Me, with one kid with shiners and, off GFCF diet she is whiney,

has focus issues, food strikes and less unprovoked speech. The other

kid is undiagnosed but had signs of apraxia and ASD. Low tone,

initial trouble producing speech, poor receptive, fine and gross

motor issues. Those things improved and some resolved on GFCF diet

and removal of bad water. Articulation issues pend.

The mom of the sensory kid went GFCF in Sept and has seen major

changes. She went to a DAN (A PhD not MD), Dr. King who operates in

conjunction with an MD, Dr. Podell, in Springfield, NJ. The mom is

healing the kid on diet but wanted to know where the kids gut was at,

if she was getting the right vitamins and minerals, using the right

probiotic, etc. She was not interested in chelation. She also wanted

alternative remedies to things that have plagued her kid in the past,

like ear stuff.

She did poop and pee tests via Drs Data and vitamin measurements via

Bioreference. She also did an IGE test. What she discovered was that

milk and wheat are an issue and some other things as well, mostly she

realized but a few, like soy and rice, must leave the diet. The

metals testing showed the worst of her stuff was actually, at this

point " high normal. " The two big things that need addressing were

aluminum and nickel. Neither are a surprise. We live in a town where

aluminum frame windows are made and then there are the vaccines.

Several industries have operated in this town so nickel is also not a

surprise.

The interesting thing was the poop test and what it told her about

what the kid was and was not getting from the current probiotic and

how to address it as well as a panel showing bacterial

susceptibilities and natural agents that could be used to address

these.

Despite giving calmag every day the kid is low in calcium.

So for $500 for the first visit, $350 paid by insurance, and another

$1500 for poop, pee, minerals, vitamin and bacterial susceptibility

tests and IGG food sensitivity testing and maybe some more for a

second visit this woman has a blueprint to treat her child. A new

probiotic was ordered, she is starting CLO, flax seed and some other

stuff tailored to her child.

So here I sit, one month shy of my son's EI age out date. There are

no preschools to take him because I waited. The town preschool that I

waived because I thought they would not abide by diet, is actually

asking the parents I was sitting with to present the GFCF diet to the

school parents as it has helped NT siblings with behavioral stuff and

parents. I can get him in there in 2 months. After what I have seen

in that meeting, where AP kids go GFCF and there problems leave

whereas my kid has aticulation stuff makes me wonder if what is left

in my guy is fluoride and lead. I need the testing. I see that now.

None of these tests seem to address fluoride which concerns me. I

will test the baby water though. At least I'll have a gauge of what

went in. I need to know the minerals, the vitamins, the flora info.

and the remedies. This is the testing we should be able to get when

we go to a mainstream dr. with a child with delays. I am scared. I am

mad. This should not have taken this long.

Hubby is on board. We are behind the 8 ball now and it is time to

catch up. Janice was right. You have to do it all:

The therapy

The diet/vitamin and mineral regimen

and

the DAN testing

You have to know what is in front of you and how to fix it. My DAN

knows the tests. Beyond that I don't know if he can give me a

blueprint like this woman got or if hers is even correct. What I do

know is I need the tests and I trust my own instincts to find someone

knowledgable and trustworthy to help me find a map from there.

[Guest guest]

We had a cheek boil that went away on its own. It was detox. Check

the drops for mercury.

I am in love with your pediatrician!

>

> Hey Liz,

>

> Dont worry. You are moving in the right direction and that is all

that

> matters. I just went to get my daughters ears rechecked and they

are fine -

> Thank goodness. So I also took Charlie and he had had what looks

like a zit

> or boil on the outside of the beginning of his inner ear. He can

now tell me

> boo boo in ear thank good ness, so I took him. Of course they gave

me an

> antiboitic and drops. I am going to give him the drops first to see

if that

> does anything then if I have to give him the antiboitic, then I

will get a

> probiotic from my dan that can out live anitboitics. I will also

call DAN!

> because perhaps it is from the detox stuff.

>

> I went back in the files and today ordered all of the tests on

apraxia. Some

> I have done and need to be retested. But with the results of the

metal

> testing coming soon and these testing we are on our way to an even

more

> taylor made version of therapy.

>

> My MD is very interested in seeing Charlie's vitamin protocol.

Impressed

> with what is happening with Charlie. Pretty openminded guy, but like

> Janice's MD from her story. Mine was much like hers, he said

literally, " I

> plead ignorance on this...Its a shame studies are not being

conducted. " All

> in all a good doc who shows interest.

>

> Colleen

> Mother of Charlie 30 months

>

>

>

> [ ] Group Meeting Results/DAN Info.

>

>

>

> Went to the group meeting in my town tonight. My town is 1/4 square

> mile, Mayberry, everyone knows everyone elses beeswax so we signed

> confidentiality agreements but are allowed to do what I am doing

now

> so long as we say, " Someone in my group. "

>

> The group is made up of parents of the following types of kids but

> not all have just speech issues and one, the only one exposed to

> fluoride in large doses, is diagnosed with dyspraxia.

>

> 1) PDD Nos, sensory issues pretty severe.

> 2) Nonverbal, PDD Nos, older sibling possible Aspergers. Going to

> Neubrander, slightly leary about him.

> 3) Me, with one kid with shiners and, off GFCF diet she is whiney,

> has focus issues, food strikes and less unprovoked speech. The

other

> kid is undiagnosed but had signs of apraxia and ASD. Low tone,

> initial trouble producing speech, poor receptive, fine and gross

> motor issues. Those things improved and some resolved on GFCF diet

> and removal of bad water. Articulation issues pend.

>

> The mom of the sensory kid went GFCF in Sept and has seen major

> changes. She went to a DAN (A PhD not MD), Dr. King who operates in

> conjunction with an MD, Dr. Podell, in Springfield, NJ. The mom is

> healing the kid on diet but wanted to know where the kids gut was

at,

> if she was getting the right vitamins and minerals, using the right

> probiotic, etc. She was not interested in chelation. She also

wanted

> alternative remedies to things that have plagued her kid in the

past,

> like ear stuff.

>

> She did poop and pee tests via Drs Data and vitamin measurements

via

> Bioreference. She also did an IGE test. What she discovered was

that

> milk and wheat are an issue and some other things as well, mostly

she

> realized but a few, like soy and rice, must leave the diet. The

> metals testing showed the worst of her stuff was actually, at this

> point " high normal. " The two big things that need addressing were

> aluminum and nickel. Neither are a surprise. We live in a town

where

> aluminum frame windows are made and then there are the vaccines.

> Several industries have operated in this town so nickel is also not

a

> surprise.

>

> The interesting thing was the poop test and what it told her about

> what the kid was and was not getting from the current probiotic and

> how to address it as well as a panel showing bacterial

> susceptibilities and natural agents that could be used to address

> these.

>

> Despite giving calmag every day the kid is low in calcium.

>

> So for $500 for the first visit, $350 paid by insurance, and

another

> $1500 for poop, pee, minerals, vitamin and bacterial susceptibility

> tests and IGG food sensitivity testing and maybe some more for a

> second visit this woman has a blueprint to treat her child. A new

> probiotic was ordered, she is starting CLO, flax seed and some

other

> stuff tailored to her child.

>

> So here I sit, one month shy of my son's EI age out date. There are

> no preschools to take him because I waited. The town preschool that

I

> waived because I thought they would not abide by diet, is actually

> asking the parents I was sitting with to present the GFCF diet to

the

> school parents as it has helped NT siblings with behavioral stuff

and

> parents. I can get him in there in 2 months. After what I have seen

> in that meeting, where AP kids go GFCF and there problems leave

> whereas my kid has aticulation stuff makes me wonder if what is

left

> in my guy is fluoride and lead. I need the testing. I see that now.

> None of these tests seem to address fluoride which concerns me. I

> will test the baby water though. At least I'll have a gauge of what

> went in. I need to know the minerals, the vitamins, the flora info.

> and the remedies. This is the testing we should be able to get when

> we go to a mainstream dr. with a child with delays. I am scared. I

am

> mad. This should not have taken this long.

>

> Hubby is on board. We are behind the 8 ball now and it is time to

> catch up. Janice was right. You have to do it all:

>

> The therapy

> The diet/vitamin and mineral regimen

> and

> the DAN testing

>

> You have to know what is in front of you and how to fix it. My DAN

> knows the tests. Beyond that I don't know if he can give me a

> blueprint like this woman got or if hers is even correct. What I do

> know is I need the tests and I trust my own instincts to find

someone

> knowledgable and trustworthy to help me find a map from there.

>

>

>

>

>

>

>

>

>

[Guest guest]

If antibiotic is needed consider a compounding pharmacy.

>

> Hey Liz,

>

> Dont worry. You are moving in the right direction and that is all

that

> matters. I just went to get my daughters ears rechecked and they

are fine -

> Thank goodness. So I also took Charlie and he had had what looks

like a zit

> or boil on the outside of the beginning of his inner ear. He can

now tell me

> boo boo in ear thank good ness, so I took him. Of course they gave

me an

> antiboitic and drops. I am going to give him the drops first to see

if that

> does anything then if I have to give him the antiboitic, then I

will get a

> probiotic from my dan that can out live anitboitics. I will also

call DAN!

> because perhaps it is from the detox stuff.

>

> I went back in the files and today ordered all of the tests on

apraxia. Some

> I have done and need to be retested. But with the results of the

metal

> testing coming soon and these testing we are on our way to an even

more

> taylor made version of therapy.

>

> My MD is very interested in seeing Charlie's vitamin protocol.

Impressed

> with what is happening with Charlie. Pretty openminded guy, but like

> Janice's MD from her story. Mine was much like hers, he said

literally, " I

> plead ignorance on this...Its a shame studies are not being

conducted. " All

> in all a good doc who shows interest.

>

> Colleen

> Mother of Charlie 30 months

>

>

>

> [ ] Group Meeting Results/DAN Info.

>

>

>

> Went to the group meeting in my town tonight. My town is 1/4 square

> mile, Mayberry, everyone knows everyone elses beeswax so we signed

> confidentiality agreements but are allowed to do what I am doing

now

> so long as we say, " Someone in my group. "

>

> The group is made up of parents of the following types of kids but

> not all have just speech issues and one, the only one exposed to

> fluoride in large doses, is diagnosed with dyspraxia.

>

> 1) PDD Nos, sensory issues pretty severe.

> 2) Nonverbal, PDD Nos, older sibling possible Aspergers. Going to

> Neubrander, slightly leary about him.

> 3) Me, with one kid with shiners and, off GFCF diet she is whiney,

> has focus issues, food strikes and less unprovoked speech. The

other

> kid is undiagnosed but had signs of apraxia and ASD. Low tone,

> initial trouble producing speech, poor receptive, fine and gross

> motor issues. Those things improved and some resolved on GFCF diet

> and removal of bad water. Articulation issues pend.

>

> The mom of the sensory kid went GFCF in Sept and has seen major

> changes. She went to a DAN (A PhD not MD), Dr. King who operates in

> conjunction with an MD, Dr. Podell, in Springfield, NJ. The mom is

> healing the kid on diet but wanted to know where the kids gut was

at,

> if she was getting the right vitamins and minerals, using the right

> probiotic, etc. She was not interested in chelation. She also

wanted

> alternative remedies to things that have plagued her kid in the

past,

> like ear stuff.

>

> She did poop and pee tests via Drs Data and vitamin measurements

via

> Bioreference. She also did an IGE test. What she discovered was

that

> milk and wheat are an issue and some other things as well, mostly

she

> realized but a few, like soy and rice, must leave the diet. The

> metals testing showed the worst of her stuff was actually, at this

> point " high normal. " The two big things that need addressing were

> aluminum and nickel. Neither are a surprise. We live in a town

where

> aluminum frame windows are made and then there are the vaccines.

> Several industries have operated in this town so nickel is also not

a

> surprise.

>

> The interesting thing was the poop test and what it told her about

> what the kid was and was not getting from the current probiotic and

> how to address it as well as a panel showing bacterial

> susceptibilities and natural agents that could be used to address

> these.

>

> Despite giving calmag every day the kid is low in calcium.

>

> So for $500 for the first visit, $350 paid by insurance, and

another

> $1500 for poop, pee, minerals, vitamin and bacterial susceptibility

> tests and IGG food sensitivity testing and maybe some more for a

> second visit this woman has a blueprint to treat her child. A new

> probiotic was ordered, she is starting CLO, flax seed and some

other

> stuff tailored to her child.

>

> So here I sit, one month shy of my son's EI age out date. There are

> no preschools to take him because I waited. The town preschool that

I

> waived because I thought they would not abide by diet, is actually

> asking the parents I was sitting with to present the GFCF diet to

the

> school parents as it has helped NT siblings with behavioral stuff

and

> parents. I can get him in there in 2 months. After what I have seen

> in that meeting, where AP kids go GFCF and there problems leave

> whereas my kid has aticulation stuff makes me wonder if what is

left

> in my guy is fluoride and lead. I need the testing. I see that now.

> None of these tests seem to address fluoride which concerns me. I

> will test the baby water though. At least I'll have a gauge of what

> went in. I need to know the minerals, the vitamins, the flora info.

> and the remedies. This is the testing we should be able to get when

> we go to a mainstream dr. with a child with delays. I am scared. I

am

> mad. This should not have taken this long.

>

> Hubby is on board. We are behind the 8 ball now and it is time to

> catch up. Janice was right. You have to do it all:

>

> The therapy

> The diet/vitamin and mineral regimen

> and

> the DAN testing

>

> You have to know what is in front of you and how to fix it. My DAN

> knows the tests. Beyond that I don't know if he can give me a

> blueprint like this woman got or if hers is even correct. What I do

> know is I need the tests and I trust my own instincts to find

someone

> knowledgable and trustworthy to help me find a map from there.

>

>

>

>

>

>

>

>

>

[Guest guest]

Aluminum replaced thimerosol in many vaccines and it was not a great

replacement. Momresearch posted on this a while back. If you can find

it in the archives it is a mustread.

Aluminum is a lighter metal and considered easier to leave so I think

(someone please correct me here if I am wrong) two things to look at

are as follows:

1) Diet: packaged foods are high in this. If he is getting too much

in and can't excrete what he already has then reduction of the

aluminum laced stuff in diet could help.

2) Immune system stuff: This may be the time to find out via genetic

testing if he has celiac or gluten sensitivity genes. The tests won't

tell you if they are turned on but will tell you if he is

predisposed. Wuth your thyroid stuff an autoimmune component would

not be out of the ordinary. If his immune system can't excrete

aluminum well then you need to look further, at gluten for one,

especially with the high B12 thing and the milk elimination respnse.

Gluten and casein are metal trappers and could be trapping the

aluminum. Genetic predisposition may make them better at it. Also,

aluminum is in a lot of gluten stuff so I often wonder when

responders do not investigate whether it is the gluten or the

aluminum or both.

Be forewarned, I think (again someone help me here) aluminum detox

involves a lot of pee.

Whatever you do, get guidance. Changing water and diet can cause

overloaded detox like we had and I'd like to see you avoid that.

> >

> > Hey Liz,

> >

> > Dont worry. You are moving in the right direction and that is all

> that

> > matters. I just went to get my daughters ears rechecked and they

> are fine -

> > Thank goodness. So I also took Charlie and he had had what looks

> like a zit

> > or boil on the outside of the beginning of his inner ear. He can

> now tell me

> > boo boo in ear thank good ness, so I took him. Of course they

gave

> me an

> > antiboitic and drops. I am going to give him the drops first to

see

> if that

> > does anything then if I have to give him the antiboitic, then I

> will get a

> > probiotic from my dan that can out live anitboitics. I will also

> call DAN!

> > because perhaps it is from the detox stuff.

> >

> > I went back in the files and today ordered all of the tests on

> apraxia. Some

> > I have done and need to be retested. But with the results of the

> metal

> > testing coming soon and these testing we are on our way to an

even

> more

> > taylor made version of therapy.

> >

> > My MD is very interested in seeing Charlie's vitamin protocol.

> Impressed

> > with what is happening with Charlie. Pretty openminded guy, but

like

> > Janice's MD from her story. Mine was much like hers, he said

> literally, " I

> > plead ignorance on this...Its a shame studies are not being

> conducted. " All

> > in all a good doc who shows interest.

> >

> > Colleen

> > Mother of Charlie 30 months

> >

> >

> >

> > [ ] Group Meeting Results/DAN Info.

> >

> >

> >

> > Went to the group meeting in my town tonight. My town is 1/4

square

> > mile, Mayberry, everyone knows everyone elses beeswax so we

signed

> > confidentiality agreements but are allowed to do what I am doing

> now

> > so long as we say, " Someone in my group. "

> >

> > The group is made up of parents of the following types of kids

but

> > not all have just speech issues and one, the only one exposed to

> > fluoride in large doses, is diagnosed with dyspraxia.

> >

> > 1) PDD Nos, sensory issues pretty severe.

> > 2) Nonverbal, PDD Nos, older sibling possible Aspergers. Going to

> > Neubrander, slightly leary about him.

> > 3) Me, with one kid with shiners and, off GFCF diet she is

whiney,

> > has focus issues, food strikes and less unprovoked speech. The

> other

> > kid is undiagnosed but had signs of apraxia and ASD. Low tone,

> > initial trouble producing speech, poor receptive, fine and gross

> > motor issues. Those things improved and some resolved on GFCF

diet

> > and removal of bad water. Articulation issues pend.

> >

> > The mom of the sensory kid went GFCF in Sept and has seen major

> > changes. She went to a DAN (A PhD not MD), Dr. King who operates

in

> > conjunction with an MD, Dr. Podell, in Springfield, NJ. The mom

is

> > healing the kid on diet but wanted to know where the kids gut was

> at,

> > if she was getting the right vitamins and minerals, using the

right

> > probiotic, etc. She was not interested in chelation. She also

> wanted

> > alternative remedies to things that have plagued her kid in the

> past,

> > like ear stuff.

> >

> > She did poop and pee tests via Drs Data and vitamin measurements

> via

> > Bioreference. She also did an IGE test. What she discovered was

> that

> > milk and wheat are an issue and some other things as well, mostly

> she

> > realized but a few, like soy and rice, must leave the diet. The

> > metals testing showed the worst of her stuff was actually, at

this

> > point " high normal. " The two big things that need addressing were

> > aluminum and nickel. Neither are a surprise. We live in a town

> where

> > aluminum frame windows are made and then there are the vaccines.

> > Several industries have operated in this town so nickel is also

not

> a

> > surprise.

> >

> > The interesting thing was the poop test and what it told her

about

> > what the kid was and was not getting from the current probiotic

and

> > how to address it as well as a panel showing bacterial

> > susceptibilities and natural agents that could be used to address

> > these.

> >

> > Despite giving calmag every day the kid is low in calcium.

> >

> > So for $500 for the first visit, $350 paid by insurance, and

> another

> > $1500 for poop, pee, minerals, vitamin and bacterial

susceptibility

> > tests and IGG food sensitivity testing and maybe some more for a

> > second visit this woman has a blueprint to treat her child. A new

> > probiotic was ordered, she is starting CLO, flax seed and some

> other

> > stuff tailored to her child.

> >

> > So here I sit, one month shy of my son's EI age out date. There

are

> > no preschools to take him because I waited. The town preschool

that

> I

> > waived because I thought they would not abide by diet, is

actually

> > asking the parents I was sitting with to present the GFCF diet to

> the

> > school parents as it has helped NT siblings with behavioral stuff

> and

> > parents. I can get him in there in 2 months. After what I have

seen

> > in that meeting, where AP kids go GFCF and there problems leave

> > whereas my kid has aticulation stuff makes me wonder if what is

> left

> > in my guy is fluoride and lead. I need the testing. I see that

now.

> > None of these tests seem to address fluoride which concerns me. I

> > will test the baby water though. At least I'll have a gauge of

what

> > went in. I need to know the minerals, the vitamins, the flora

info.

> > and the remedies. This is the testing we should be able to get

when

> > we go to a mainstream dr. with a child with delays. I am scared.

I

> am

> > mad. This should not have taken this long.

> >

> > Hubby is on board. We are behind the 8 ball now and it is time to

> > catch up. Janice was right. You have to do it all:

> >

> > The therapy

> > The diet/vitamin and mineral regimen

> > and

> > the DAN testing

> >

> > You have to know what is in front of you and how to fix it. My

DAN

> > knows the tests. Beyond that I don't know if he can give me a

> > blueprint like this woman got or if hers is even correct. What I

do

> > know is I need the tests and I trust my own instincts to find

> someone

> > knowledgable and trustworthy to help me find a map from there.

> >

> >

> >

> >

> >

> >

> >

> >

> >

[Guest guest]

Good choice Colleen,

I would wait some time before using something so strong on our little

Charlie....slow and gentle is absolutely the way to go. I'm becoming very fond

of him.... please post pictures someday....

Janice

[ ] Group Meeting Results/DAN

Info.

> > >

> > >

> > >

> > > Went to the group meeting in my town tonight. My town is 1/4

> square

> > > mile, Mayberry, everyone knows everyone elses beeswax so we

> signed

> > > confidentiality agreements but are allowed to do what I am

doing

> > now

> > > so long as we say, " Someone in my group. "

> > >

> > > The group is made up of parents of the following types of

kids

> but

> > > not all have just speech issues and one, the only one

exposed to

> > > fluoride in large doses, is diagnosed with dyspraxia.

> > >

> > > 1) PDD Nos, sensory issues pretty severe.

> > > 2) Nonverbal, PDD Nos, older sibling possible Aspergers.

Going to

> > > Neubrander, slightly leary about him.

> > > 3) Me, with one kid with shiners and, off GFCF diet she is

> whiney,

> > > has focus issues, food strikes and less unprovoked speech.

The

> > other

> > > kid is undiagnosed but had signs of apraxia and ASD. Low

tone,

> > > initial trouble producing speech, poor receptive, fine and

gross

> > > motor issues. Those things improved and some resolved on

GFCF

> diet

> > > and removal of bad water. Articulation issues pend.

> > >

> > > The mom of the sensory kid went GFCF in Sept and has seen

major

> > > changes. She went to a DAN (A PhD not MD), Dr. King who

operates

> in

> > > conjunction with an MD, Dr. Podell, in Springfield, NJ. The

mom

> is

> > > healing the kid on diet but wanted to know where the kids

gut was

> > at,

> > > if she was getting the right vitamins and minerals, using

the

> right

> > > probiotic, etc. She was not interested in chelation. She

also

> > wanted

> > > alternative remedies to things that have plagued her kid in

the

> > past,

> > > like ear stuff.

> > >

> > > She did poop and pee tests via Drs Data and vitamin

measurements

> > via

> > > Bioreference. She also did an IGE test. What she discovered

was

> > that

> > > milk and wheat are an issue and some other things as well,

mostly

> > she

> > > realized but a few, like soy and rice, must leave the diet.

The

> > > metals testing showed the worst of her stuff was actually,

at

> this

> > > point " high normal. " The two big things that need addressing

were

> > > aluminum and nickel. Neither are a surprise. We live in a

town

> > where

> > > aluminum frame windows are made and then there are the

vaccines.

> > > Several industries have operated in this town so nickel is

also

> not

> > a

> > > surprise.

> > >

> > > The interesting thing was the poop test and what it told her

> about

> > > what the kid was and was not getting from the current

probiotic

> and

> > > how to address it as well as a panel showing bacterial

> > > susceptibilities and natural agents that could be used to

address

> > > these.

> > >

> > > Despite giving calmag every day the kid is low in calcium.

> > >

> > > So for $500 for the first visit, $350 paid by insurance, and

> > another

> > > $1500 for poop, pee, minerals, vitamin and bacterial

> susceptibility

> > > tests and IGG food sensitivity testing and maybe some more

for a

> > > second visit this woman has a blueprint to treat her child.

A new

> > > probiotic was ordered, she is starting CLO, flax seed and

some

> > other

> > > stuff tailored to her child.

> > >

> > > So here I sit, one month shy of my son's EI age out date.

There

> are

> > > no preschools to take him because I waited. The town

preschool

> that

> > I

> > > waived because I thought they would not abide by diet, is

> actually

> > > asking the parents I was sitting with to present the GFCF

diet to

> > the

> > > school parents as it has helped NT siblings with behavioral

stuff

> > and

> > > parents. I can get him in there in 2 months. After what I

have

> seen

> > > in that meeting, where AP kids go GFCF and there problems

leave

> > > whereas my kid has aticulation stuff makes me wonder if what

is

> > left

> > > in my guy is fluoride and lead. I need the testing. I see

that

> now.

> > > None of these tests seem to address fluoride which concerns

me. I

> > > will test the baby water though. At least I'll have a gauge

of

> what

> > > went in. I need to know the minerals, the vitamins, the

flora

> info.

> > > and the remedies. This is the testing we should be able to

get

> when

> > > we go to a mainstream dr. with a child with delays. I am

scared.

> I

> > am

> > > mad. This should not have taken this long.

> > >

> > > Hubby is on board. We are behind the 8 ball now and it is

time to

> > > catch up. Janice was right. You have to do it all:

> > >

> > > The therapy

> > > The diet/vitamin and mineral regimen

> > > and

> > > the DAN testing

> > >

> > > You have to know what is in front of you and how to fix it.

My

> DAN

> > > knows the tests. Beyond that I don't know if he can give me

a

> > > blueprint like this woman got or if hers is even correct.

What I

> do

> > > know is I need the tests and I trust my own instincts to

find

> > someone

> > > knowledgable and trustworthy to help me find a map from

there.

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >