DAN Doctors

[Guest guest]

> So here is the question can I start enzymes with the same results

> without doing the diet??

For many kids, yes. Some kids still need food removals tho. You can

certainly try doing enzymes without diet, see if it works for your child.

Dana

[Guest guest]

Well, they told me that to. They said there is nothing anyone could do for

my special needs child other than psych meds. Well, they were 100% wrong.

He is no longer on psych meds and now in regular school with no modifications.

Only listen to those who have been successful. If someone says your child

can't be helped, then they can not help them. Go to those who can. I

remember the first things I tried were digestive enzymes and Ginger Root, just

to

see if my son could be helped. WOW, DOUBLE WOW, just on those two things. I

knew then that all this stuff I was reading on the web was true.

Heidi N

************************************** See what's new at http://www.aol.com

[Guest guest]

Hi ,

I don't post regularly here, but I saw " Tulsa " and thought I would

respond. I'm originally from there, but living overseas at the moment.

We searched for a DAN doctor in the Tulsa area and found one in Jenks--

it's listed on the ARI site of DAN doctors. But, we never went to him

as we were getting along OK without a doc and decided to save some

money. So I don't have any personal experience with this doc to advise

you.

Also, after reading the recommendations for DAN docs on one of these

message boards, I have decided that if we ever do go to one I would

use a doc in Kansas City with at least 20 years of experience treating

ASD kids. His name is Dr. Baptist. I mention this because I

want to make you aware that just because a doctor is on the DAN list

doesn't necessarily mean they are a good DAN doc--have read some

stories on these message boards over the years that were negative and

made me want to make sure I was using an experienced practitioner.

http://www.autismwebsite.com/practitioners/danus.html

This is the list of DAN's for the US.

Good luck,

Satia

> I am searching for a DAN doctor in Tulsa Oklahoma. My pediatrician

said

> that all of the bio-chemical stuff is useless, but I do not believe

> that. I am looking for someone who can educate me, and help my son.

> Thank You,

>

>

[Guest guest]

When I give my kids supplements, this is how I dose. Many supplements

bought from companies who specialize in making supplements for special needs

kids,

have recommended doseage on them. When, I buy a herb from the store or net

that is from a general company, I take what they say myself, and see how I

feel. If I like the recommended dose for me, I half it for my 10 year old, and

1/3 it for my 5 year olds. I also research much on the net about safety and

side effects. The herbs I always use have no bad side effects unless you

were to take gobs or were on meds. I occasionally take herbs for short periods

of time that may have side effects, but I always take them with milk thistle

to help with that. Thus, you have to research each herb and also take it

yourself. Plus, give small amounts at first and then work up to a recommended

dose, sometimes, depending. At my house, I take 550mg Ginger Root twice a

day. I take a digestive enzyme 3 times a day. I just give them to my kids

twice a day due to the fact that I have to work around school. I try to keep

all supplements on the once or twice a day regime to make it easier to work

around school, and it works for me. Now I send gf-cf lunches to school for my

5

year old so they don't have to take enzymes at lunch. My 15 year old does

not each lunch because he is too embarrassed to pack a lunch.

Heidi N

************************************** See what's new at http://www.aol.com

[Guest guest]

Thanks for the reply. My son is 5 and about 40LBS. How much? and what kind?

These are my never ending questions. I am completely new to all of this, and I

am incapable for some reason of figuring out what to give my son. I guess it is

obvious that my doctor is of no help.

Proud Mother of

---- Ambitionn01@... wrote:

> Well, they told me that to. They said there is nothing anyone could do for

> my special needs child other than psych meds. Well, they were 100% wrong.

> He is no longer on psych meds and now in regular school with no

modifications.

> Only listen to those who have been successful. If someone says your child

> can't be helped, then they can not help them. Go to those who can. I

> remember the first things I tried were digestive enzymes and Ginger Root,

just to

> see if my son could be helped. WOW, DOUBLE WOW, just on those two things. I

> knew then that all this stuff I was reading on the web was true.

>

> Heidi N

>

>

>

> ************************************** See what's new at http://www.aol.com

>

>

>

[Guest guest]

http://health.groups.yahoo.com/group/SillyYaks/

The above is an awesome group.

Also, this drink may be interesting for you:

http://www.neocate.com/aaa_neocate/703-neocate-products-E028-splash.html

Finally, we are starting feeding therapy next Friday so that's

probably my default suggestion to everyone for the next 6 mos, lol!

It's generally done by a speech language pathologist, anyone like that

near you?

Debi

[Guest guest]

http://health.groups.yahoo.com/group/SillyYaks/

The above is an awesome group.

Also, this drink may be interesting for you:

http://www.neocate.com/aaa_neocate/703-neocate-products-E028-splash.html

Finally, we are starting feeding therapy next Friday so that's

probably my default suggestion to everyone for the next 6 mos, lol!

It's generally done by a speech language pathologist, anyone like that

near you?

Debi

[Guest guest]

http://health.groups.yahoo.com/group/SillyYaks/

The above is an awesome group.

Also, this drink may be interesting for you:

http://www.neocate.com/aaa_neocate/703-neocate-products-E028-splash.html

Finally, we are starting feeding therapy next Friday so that's

probably my default suggestion to everyone for the next 6 mos, lol!

It's generally done by a speech language pathologist, anyone like that

near you?

Debi

[Guest guest]

i just put in a request to join this group, might be good for my daughter with

celiacs.

Cheryl S [chez]

To: Autism_in_Girls@...: fightingautism@...: Wed, 1

Oct 2008 23:35:46 +0000Subject: Re: DAN Doctors

http://health.groups.yahoo.com/group/SillyYaks/The above is an awesome

group.Also, this drink may be interesting for

you:http://www.neocate.com/aaa_neocate/703-neocate-products-E028-splash.htmlFina\

lly, we are starting feeding therapy next Friday so that'sprobably my default

suggestion to everyone for the next 6 mos, lol!It's generally done by a speech

language pathologist, anyone like thatnear you?Debi

_________________________________________________________________

[Guest guest]

i just put in a request to join this group, might be good for my daughter with

celiacs.

Cheryl S [chez]

To: Autism_in_Girls@...: fightingautism@...: Wed, 1

Oct 2008 23:35:46 +0000Subject: Re: DAN Doctors

http://health.groups.yahoo.com/group/SillyYaks/The above is an awesome

group.Also, this drink may be interesting for

you:http://www.neocate.com/aaa_neocate/703-neocate-products-E028-splash.htmlFina\

lly, we are starting feeding therapy next Friday so that'sprobably my default

suggestion to everyone for the next 6 mos, lol!It's generally done by a speech

language pathologist, anyone like thatnear you?Debi

_________________________________________________________________

[Guest guest]

i just put in a request to join this group, might be good for my daughter with

celiacs.

Cheryl S [chez]

To: Autism_in_Girls@...: fightingautism@...: Wed, 1

Oct 2008 23:35:46 +0000Subject: Re: DAN Doctors

http://health.groups.yahoo.com/group/SillyYaks/The above is an awesome

group.Also, this drink may be interesting for

you:http://www.neocate.com/aaa_neocate/703-neocate-products-E028-splash.htmlFina\

lly, we are starting feeding therapy next Friday so that'sprobably my default

suggestion to everyone for the next 6 mos, lol!It's generally done by a speech

language pathologist, anyone like thatnear you?Debi

_________________________________________________________________

[Guest guest]

Hi Becky,

My daughter is 6 also and I took her to 2 different DAN drs. in the past.

Because they are so expensive, I decided to go and get the lab tests needed as

well as have the dr. put my daughter on her initial group of supplements. From

there, once the tests results were back and I knew what was going on in my

daughters system, I did a lot of reading and kind of started trying different

supplements and protocals on my own. That was all done after seeing the first

DAN dr. After about a year, I then went to another DAN that was closer to me

and redid some of the initial tests to see if there were any changes and I

allowed her (the second dr.) to rework the supplements/dosages that my daughter

was on, due to the results of the second group of labs. After that, again I

went on my own with finding things that worked for my daughter.

I have found that once you are familiar with many of the basic supplements along

with some specifically tailored to your child, the dr. part is not as pertinent

unless you need a rx. prescription such as Diflucan, Valtrex, mb12 injections,

etc. And also, you may want to keep in mind that Stan Kurtz, who is BIG in the

world of autism did not have a DAN dr. when he was trying to recover his son

(who is now recovered). He went through trial and error, and had a good

pediatrician.

Probably not much help, just something to think about.

Karmen

DAN Doctors

I have a 6 year old daughter that was diagnosed when she was 3. Many

of you mention taking your children to DAN Dr's. I have never heard of

them other then here. Where do I find them, or does your Pedeatrition

have to refer you?

Becky

In South GA

[Guest guest]

Hi Becky,

My daughter is 6 also and I took her to 2 different DAN drs. in the past.

Because they are so expensive, I decided to go and get the lab tests needed as

well as have the dr. put my daughter on her initial group of supplements. From

there, once the tests results were back and I knew what was going on in my

daughters system, I did a lot of reading and kind of started trying different

supplements and protocals on my own. That was all done after seeing the first

DAN dr. After about a year, I then went to another DAN that was closer to me

and redid some of the initial tests to see if there were any changes and I

allowed her (the second dr.) to rework the supplements/dosages that my daughter

was on, due to the results of the second group of labs. After that, again I

went on my own with finding things that worked for my daughter.

I have found that once you are familiar with many of the basic supplements along

with some specifically tailored to your child, the dr. part is not as pertinent

unless you need a rx. prescription such as Diflucan, Valtrex, mb12 injections,

etc. And also, you may want to keep in mind that Stan Kurtz, who is BIG in the

world of autism did not have a DAN dr. when he was trying to recover his son

(who is now recovered). He went through trial and error, and had a good

pediatrician.

Probably not much help, just something to think about.

Karmen

DAN Doctors

I have a 6 year old daughter that was diagnosed when she was 3. Many

of you mention taking your children to DAN Dr's. I have never heard of

them other then here. Where do I find them, or does your Pedeatrition

have to refer you?

Becky

In South GA

[Guest guest]

Don, I don't know & don't need to know the name of your DAN, but let

me say not all DANs are created equal. I saw 2 crappy ones before I

saw a good one. And, among those highly regarded they aren't effective

for all people all the time. Sometimes it may be a personality issue

as much as anything. Just wanted to share because while biomed doesn't

help every person with autism, sometimes a bad doc may keep kids who

would respond away.

Debi

[Guest guest]

Don, I don't know & don't need to know the name of your DAN, but let

me say not all DANs are created equal. I saw 2 crappy ones before I

saw a good one. And, among those highly regarded they aren't effective

for all people all the time. Sometimes it may be a personality issue

as much as anything. Just wanted to share because while biomed doesn't

help every person with autism, sometimes a bad doc may keep kids who

would respond away.

Debi

[Guest guest]

Don, I don't know & don't need to know the name of your DAN, but let

me say not all DANs are created equal. I saw 2 crappy ones before I

saw a good one. And, among those highly regarded they aren't effective

for all people all the time. Sometimes it may be a personality issue

as much as anything. Just wanted to share because while biomed doesn't

help every person with autism, sometimes a bad doc may keep kids who

would respond away.

Debi

[Guest guest]

Hi Ricky,

We have seen Jeanne Hubbuch in Newton, who I think is very good. She is very

even-keeled and empathetic, and seems to be pretty knowledgeable, really listens

and doesn't force her recommendations if you are not comfortable with them.

Like most DANs she does not accept insurance, which was a hurdle for us. Also,

communication with her office is not the best (e.g. I would call or email

her/the office with a question, and not get an answer for 3-4 days.

If you do use her, be cautious of the chelation aspect if you get to that point.

She recommended zeolites for my daughter (we never used). She is familiar with

the AC protocol, does not think the chelators need to be dosed every 3 hrs. But

was not averse to us doing it either.

We have also seen Hardy in Hingham briefly. I did not think he was as

knowledgeable, got the feeling I was driving the process, not him. JMO though.

Good luck

>

> Does anyone know any good Dan doctors in the Boston area? Thanks.

>

> Ricky

>

>

>

>

>

[Guest guest]

Thanks !

________________________________

From: khieken <khieken@...>

Sent: Sun, June 27, 2010 9:55:35 AM

Subject: [ ] Re: Dan Doctors

 

Hi Ricky,

We have seen Jeanne Hubbuch in Newton, who I think is very good. She is very

even-keeled and empathetic, and seems to be pretty knowledgeable, really listens

and doesn't force her recommendations if you are not comfortable with them.

Like most DANs she does not accept insurance, which was a hurdle for us. Also,

communication with her office is not the best (e.g. I would call or email

her/the office with a question, and not get an answer for 3-4 days.

If you do use her, be cautious of the chelation aspect if you get to that point.

She recommended zeolites for my daughter (we never used). She is familiar with

the AC protocol, does not think the chelators need to be dosed every 3 hrs. But

was not averse to us doing it either.

We have also seen Hardy in Hingham briefly. I did not think he was as

knowledgeable, got the feeling I was driving the process, not him. JMO though.

Good luck

>

> Does anyone know any good Dan doctors in the Boston area? Thanks.

>

> Ricky

>

>

>

>

>

[Guest guest]

Really just wondering what people think about DAN Doctors?

I never really met anyone in the middle. Either they are all for them or not at

all. Most in medical field I have encounter seem to think there isn't enough

research yet.

Sent from my iPhone

On Mar 8, 2011, at 12:55 PM, " kiddietalk " <kiddietalk@...> wrote:

> Marie most of us checked out NV with our child's pediatric medical doctor- you

can use the information here http://pursuitofresearch.org/find-a-professional/

There is much information about this in the archives. It's just food, all

essential nutrients are from food, so not like taking a supplement which can

have issues -thus makes it easier to approve. (kind of like approving water)

>

> About speak- there is also much information about this in the archives-

including recently so as it's a sore spot for many here who's children had

horrific side effects on speak- we don't go into details. But please look up

hypervitaminosis in regards to the amounts of vitamin e and k in the product.

Also, this group had experience over a period of 2 years with primarily 200 to

400 IUs of vitamin e- there were to my knowledge only a handful of parents

working direct with either Dr. or Dr. Agin -Cheryl was one of them for

her daughter Shea who at 4 years old was put on (Cheryl jump in if I'm getting

the dosage wrong) but 1000 IU of vitamin e- and I don't know the exact amounts

but mega amounts of vitamin k as well. Basically Shea was put on the speak

formula but prior to speak existing and by the doctor that formulated it with

her theory of vitamin e. From the formula of speak- Cheryl's daughter started

having psychotic episodes as you can find the archives which di d not cease- and

she was not progressing without regressing again until NV as is also in the

archives.

>

> Below is a recent message from a parent of a two year old that did know about

the side effects in others from this group -but Ivy tried the one month special

from the speak company anyway -and the following is a recent topic between us.

Again much more in the archives -but I'm sure there is much in the following as

well.

>

> ~~~first message from Ivy -then me- then Ivy

>

> Oh my gosh! Thank you for this message back to me. I am so sickened with anger

and disgust, and cannot believe I gave that product to him. I am so concerned

now, and have much to look into. The doctor (we don't see currently) who

approved us using it, my son was little and underwt last year, saw the amt of E

and K in it and said " go ahead " . Wow, and my little guy did all four caps

weighing about 26lbs.

>

> I know that my son did awful on the SPEAK product, yet I never made the

connection that his regression was cause by it. He didn't go totally silent

after that oil, but definately lost all gains in speech and never could get back

up. IF it had been a dead-stop halt on everything or such bad groping coming out

of his mouth, it would have been much clearer to me.

>

> Disgusted is what i am now. Also, maybe have a direction to seek help going

forward..so many unanswered questions as to his regression have been drilling my

head. Thank you again for shedding light on this. I see Tanner took 7 months to

get back to where he was before SPEAK. My son is 13 months since..and not

getting better. NV, yes, will put him back on this AM. BTW i think i never

answered you when you asked what else my son was on when he did the NV trial..he

was only on a homeopathic remedy, which doesnt matter now..since we may have

answer to this whole situation.

>

> I never saw seizures. Yet i should look up the date when he started rubbing

his forehead..since he doesnt sign " pain/owie " and doesnt point to painful

areas..what if he HAS been getting headaches? He is a kind gemtle child,

cooperative..yet somedays he throws toys outta nowhere and i always attributed

it as yeast/bacteria. (we are having a stool test done this next week because of

all of the symptoms i mentioned). Homeopathy has gotten him to come running to

me with semi-disturbed tears when hurt or to complain about his brother..that

area has improved!

>

> My son never really feels pain as much as other kiddos..and when he is hurt,

he shows pain for a fraction of time..much less than other kids. He feels it,

but gets over it fast. WHAT if he has headaches and doesnt attribute the pain,

discomfort, to tnat and acts out? I cannot give a reason to the head rub he

does.

> How do i know if he has headaches?

> How long to heal from effects of that nasty oil?

>

> WHAT else do I do to help him? EEG to check for seizures? How do i fix and

check for " hypervitaminosis " ? And is it only the vit E..what about the K..how do

I check..especially since so long ago taken?

>

> Okay going to read up on stuff. Scared a bit at what happened to him..all

possibly because of that product.

>

> Thanks for shedding light,

> Ivy

>

>

>

> Oh Ivy!!! I'm so sorry!!! Now it all makes sense -I was so confused before and

now it makes sense!!!

>

> My son who was way 11 years old -way older than yours. in less than 2 weeks

(so half the time you had your child on pharma omega speak) regressed to where

he couldn't say ANYTHING on this same product and it took 7 months to be

anywhere back to normal. I still get a knot in my stomach thinking of the poor

little guy standing in our driveway when he opened his mouth to say something

and nothing at all came out -and the look of horror on his face -he regressed

back from 11 years old all the way to before he was on fish oils at 2. I have

gone into detail about this as I've outlined my son's severe regression many

times here and how I had to go to his school where he was doing so incredible

and speak to the entire school -teachers, students, head of school all there

about Tanner-with Tanner there. It had gotten around that I put Tanner on an

" exploratory drug " and nobody could figure out why Tanner had trouble saying

even simple words -when prior to pharma omega speak - this is how he was

speaking http://www.debtsmart.net/talk/tanner.html In addition to Tanner's

horrific regression in speech- Tanner's grade PLUMMETED from mainly As and a few

Bs to Ds -he suddenly found the school work difficult that he was able to do

prior. This was after again less than 2 weeks on pharma omega speak. Tanner

wasn't put on NV until about 2 years after pharma omega speak and all that know

Tanner -family, friends and professionals credit NV for not only bringing Tanner

back -but he's so beyond where he was prior -he's excelling beyond the norm in

so many areas now!

>

> While I (or you for that matter) don't know if there were seizures from this

product unless you witnessed it or tested for it, quite a few parents reported

that their children had seizures from this product pharma omega speak that never

had seizures prior. We have used fish oils of all dosages in this group for over

ten years -myself included -at one point Tanner was up to 9 capsules and Dakota

(my ADHD son) up to 10 fish oil capsules a day- and doing great as you can tell

from the recordings of Tanner above. By the way the other thing Tanner developed

after being on pharma omega speak was severe headaches. Do you know if your

child gets headaches? There is a list of side effects in this group and I

believe here as well

http://www.facebook.com/topic.php?uid=115029735601 & topic=7363

>

> I personally am shocked that pharma omega speak is still on the market and it

sickens me to my stomach when I think that (to me) I poisoned my son with

vitamin E and K. You may want to again read the following page

> http://www.facebook.com/topic.php?uid=115029735601 & topic=7363

>

> And to read all the reports compiled from this group after trying pharma omega

speak which was overwhelmingly negative you may want to read this from our link

section

/links/Pharma_Omega_Spea\

k_reports_from_group_001224703760/

>

> PLEASE don't take your child off NV Ivy!!!!! Again now that you shared this.

Now it all makes sense to me where I was clearly so confused before! That's what

I was trying to find out -why did your son regress it just didn't make sense!

>

> You absolutely need to take all the information above to your child's doctors

and have your child tested to see if there are any signs of neuro damage since

being on pharmaomega speak.

>

> Look up the words " hypervitaminosis E " and check the meta analysis which shows

vitamin e toxicity and links to giving even an adult 400 IU of vitamin E

increase death for various reasons. Please check the " upper tolerable level "

here at this NIH site and you'll see your child should not have any more than

300 IU of vitamin E http://ods.od.nih.gov/factsheets/vitamine/ Each speak

capsule from what I can remember has 200 IU of alpha vitamin E and 100 IU of

gamma vitamin E. Your child got at least double over the amount of vitamin E.

>

> Before you told me this, as I wrote in the one email, I would have agreed with

that one doctor to stop NV as nothing has made a difference with all the

therapies, therapists, alternative treatments...it all didn't make sense- but

again now it does- and please don't stop NV now that I know!!! Ivy NV is the

only thing that brought my son Tanner back to where he was prior to that being

put on that (in my opinion and yes I'm going to scream it!!!) CRAP!!!!! And my

son was only on it for less than 2 weeks. Not only did NV bring him back but I

thank God every day that he's had such tremendous surges in areas that were

above and beyond from before. Tanner just happened to be in the same school with

the same professionals -one of them highly respected in education in my area of

Florida (Tanner's school was one of the 2 from Florida invited to the

inauguration no matter who became president) It was this head of school after

Tanner was on NV for one week that called me up in shock over the changes in

Tanner in speech and academics -specifically reading non stop and being alert

and focused and participating in class- noticed by all in the school -sudden

dramatic change. Also Tanner effortlessly normalized in weight very quickly -he

lost 6 pounds in 5 days where he never lost a pound prior and 9 pounds in 2

weeks -then he shot up -at one point he grew taller and had lost 15 pounds- he's

now slightly over 6 foot tall at 14 years old and around 180 pounds. he's become

I'd say even graceful in playing basketball and football- he's a different

person. He's independent -all the areas of surge I have here

http://pursuitofresearch.org/pursuit-of-research/

>

> I believe that pharma omega speak created both neurodamage and damage to my

child's metabolic system. THAT is the reason I put my son on NV to begin with

for those that wonder " who in the world would put their child on a product that

was formulated for weight management in adults? " My son was 5 7 and 162 at 13

years old -2 years after that product and no matter how well he ate and how much

he exercised he just kept gaining weight. I have this in the history here

http://pursuitofresearch.org/the-history-why-nutriiveda-for-therapeutic-use-for-\

autism-apraxia-etc/

>

> And for those reading this -if your child has a growth disorder, failure to

thrive and is put on NV -read the reports that the same child will have growth

in height and weight/muscle. These are all the conditions that have not just

parental but professionals anecdotal feedback of positive surges once on NV

Autism Spectrum Disorder, Apraxia, Dyspraxia, Dysarthria, Undiagnosed Speech

Delay, Language Disorder, Asperger Syndrome, ADHD, CAPD, Traumatic Brain Injury,

Seizure Disorders, Epilepsy, Metabolic Disorder, Delayed Myelinazation, Cerebral

Palsy, Tic Disorders, Growth Disorders, Failure To Thrive, Hypotonia, Mild

Periventricular Leukomalacia, Genetic Syndrome, Chromosomal Abnormalities,

Sensory Integration Dysfunction, Cognitive Impairment, Mental Retardation,

Congenital Insensitivity To Pain With Anhidrosis (CIPA) Rare Genetic Disorder,

Agenesis Of Corpus Callosum (Congenital Disorder) Global Delays and even in

Alzheimer's Disease

>

> And we even in our survey have have reports of surges in those children with

undiagnosed speech delays http://pursuitofresearch.org/survey/

>

> The other thing that is very interesting is the high number of older children,

teens and even young adults. It does not appear to matter what age you start NV

to see results -Clearly Teri's 89 year old father who suffered from Alzheimer's

for 9 years is a clear indication of that too!!

http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift-\

in-diseases-of-the-elderly/

>

> In this past year based on my son and SO many others, and based on research on

the foods in NV, I now believe that NV both supports the metabolic system and

creates neuro repair. In regards to the metabolic system - who's 5 and a

half year old son's remarkable surge from severe profound to mild moderate

apraxic in 3 months (yes you read that right -THREE months!!) documented by the

child's SLP and neurologist from Kent University as " must be a combination of

therapy and Nutriiveda " and what will tell you is that her son was

getting 2 days a week of therapy at Kent University and after being put on NV

the therapy was cut to once a week -and yet he still had that surge!

>

> Well another update is that this same child's neurologist did blood testing

since being on NV and now all nutritional levels that were low before are

normalized and this one test which had a range say of 4 to 11 or something - any

higher being really bad -well her son was one below the lowest number. So the

mom asked the neurologist what that meant...and you ready?? The neurologist said

" that just means your child's metabolism is working better than the average

person " She is mailing me the entire report so I can take out names and put that

up here on the same page where her child's professional anecdotal report from

Kent University of the remarkable surge from basically profound to mild apraxia

in 3 months is

http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift-\

in-treatment-of-speech-impairments/

>

> Please email me in private- lisa@ I would like to talk to you to help you help

your child. I want to talk to you a bit more about dosage considering the

situation so you can talk to your child's doctor. Oh and by the way -the study

that Jeanne just posted here yesterday about serotonin links to autism -I

updated our page which talks about this one essential amino acid

http://pursuitofresearch.org/2010/11/24/dont-let-the-turkeys-get-you-down-becaus\

e-they-cant/

>

> When you supplement you only get a fraction of the nutrient -perhaps 10 to 30

percent...when you get that same nutrient in food you absorb typically 100

percent. That in itself may be why NV is helping our kids -the essential amino

acid it contains from food are linked to neuro repair

http://pursuitofresearch.org/2010/10/15/two-new-studies-choice-is-diet-or-drugs-\

to-help-tbitraumatic-brain-injury-research-amino-acids/ and the entire product

was formulated by world renowned medical doctors

http://pursuitofresearch.org/endorsed-by-the-chopra-center/ to support the

metabolic system- and as I wrote above we know that's working the way it

should!!

>

> I am so sorry I didn't know your child was ever on pharma omega speak...again

I was so confused but now it all makes sense to me!! And yes I do believe there

is hope Ivy -based on what I have seen in my son Tanner, and now that I know

what your child is dealing with - I so believe that!!!

>

> Hugs,

>

>

>

> =====

>