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RE: New video after 6mos on NutriiVeda

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Wow Sharon both to the surges and to the job you have done in documenting this

journey. Most who are not parents or professionals that deal with apraxia won't

be as impressed by the dramatic surges because most don't appreciate what a

long, slow, intensive speech therapy almost daily road to see even a glimmer of

progress road apraxia typically is. The average person would be more moved by

an older child or teen as they probably look at this and think " cute " but think

he's just " talking like a baby " You see for most -it goes from " he's just a

late talker " to " what's wrong with him " by around the age of 4 years old. I

think you just may be able to skip the horrible stage I and many of us had to go

through -the " what's wrong with him? " stage where perfect strangers believe it

appropriate to ask you that question in public and right in front of your

precious child!!

Not only is this remarkable what you did -but even for the public that is still

cluelesss -I think this will be one of the greatest ways to bring awareness to

just what we as parents go through in raising an apraxic child -how we have to

translate for them, and we can. It also shows not all that can't talk are

autistic. clearly is not autistic but clearly is speech impaired and

desperately is trying to talk to you. And by the way Missy -you missed your

calling as a teacher -OMG you are so amazing!!!

These videos bring to light all the times when Tanner was little where he would

talk and people would look at me (his translator :)

And once again if apraxia had physical characteristics...for sure it means ultra

adorable!!!! What a cutie pie!!!

Before I go into my observations just wanted to point out a few technical

difficulties I had because I don't know if it was just my computer. The video

under 2 weeks after nutriiveda where is wearing the white shirt (second one

down there) it starts and stops -so either it's my computer or it's not loaded

right.

Also the video under 3 months -also the second one down -where is singing

" you are my sunshine " I recall that being longer than a sentence -did it get cut

short or did you cut it short?

Also just want to point out that CHERAB is with an 'A' (for apraxia) because you

have it with a U :)

My observations

1. While I rarely understood him in previous videos without your help or visual

cues -his speech and articulation...OMG what a tremendous difference!!!

2. Because you don't clarify what's what I have no idea if the surge is from

nutriiveda or the other new thing you just added as you don't really specify how

long and what exactly you are doing with it. To see that tremendous of a surge

in a few months is just amazing. I think you need to break down exactly what

created what surge. I typically waited at least 3 months before adding new

therapies so new and could explain what surges were from what therapies. The

way the blog is now if I was to read it for the first time I'd be a bit

overwhelmed in knowing what to do- what helped the most. In fact based on the

progression it appears since the 6 month update is the most dramatic and recent

that it may have to do with NAET treatments (never did them with Tanner so

unknown to me) How many did you do? I find the fish oils (the essential fatty

acids) to compliment the essential amino acids because both are essential

nutrients. You say the NAET compliments nutriiveda -what is it and how? It

would be good if you can break this down a bit more as again it's hard to know

why he surged so much again between 3 and 6 months and based on what you wrote

it looks like it's the combination...but would he have surged without NAET?

What if....now this is just a thought but I love to do this when people credit

other therapies to surges and I have done this for years with the fish

oils...you keep doing NAET...but stop the nutriiveda for a few days and document

that via video update. To me right now that is the only way of knowing what is

doing what as again it's not clear.

No matter what 's articulation, ability to correct himself when you ask,

talk on command -that's all just amazing.

My suggestion other than trying to stop nutriiveda and just using this other new

thing for a few days...is to teach how to use his toys to motor plan. From

3 years old I had Tanner using either his hands- or two toys to motor plan words

that he didn't know how to say. is talking so much and from what I was

taught by his SLPs over the years you don't want to get things into the motor

memory wrong -and it appears like with the word " tree " that says it the way

he does because it's in his motor memory that way -so comfortable. But if

he/you were to take one tree and hold it up and say " t " " t " " t " (3 times is the

magic amount I've been told) and then take another tree and hold it up and say

" ree " " ree " " ree " and have him repeat..;then take the one tree he is holding

-the " t " tree and say " t " and the " ree " tree and slowly move them together

saying as they got closer and closer " t " " ree " " t " " ree " and then saying " tree "

that is the way we taught Tanner how to correct.

I was extremely impressed with his alphabet and to me it appears he is working

extra hard in making sure his articulation for the letters was perfect.

Sharon once again this website and all you have done is just incredible and

beautiful. Please don't think I'm being hard on you by pointing out anything

-and please feel free to change or not change based on what you think is best.

I used to be an art director and worked in media and the film industry and I

myself LOVE constructive criticism as that's how we can learn to improve. I

used to hate when someone would look at something I did and just say " wow that's

great " I'd always say " well what can be improved? "

Funniest was one day someone said to me " you always say you love constructive

criticism. What's the difference between criticism and constructive criticism? "

:)

My answer and this is a for real quote

:)

" Criticism is when someone says 'you suck' and constructive criticism is when

someone says 'you suck because' "

Anyway in conclusion to add one more thing -I'd have a written evaluation from

your child's SLP included on this page. All of it right now is parental

anecdotal and what we can see -your child's SLP will be awesome in providing a

professional look at what's going on.

I just heard from Barbara SLP yesterday about a parent who took her child

off nutriiveda after a few months and didn't tell her- but the child had a

complete regression in both behavior and speech -ability to imitate etc.

Barbara specifically asked " did you give him his nutriiveda? " and that is when

she found out the parents took the child off for a few days to see if it still

made a difference (did) so of course put him back on and within one day he had

tremendous surges back again. Barbara is thinking of writing a case study on

this. That's what I mean -if your child's SLP is able to write something

up...just like I posted there is going to be a written report from a neurologist

from Kent University where the doctor and SLP both credit nutriiveda (and

therapy of course too) to the child going from profound to mild/moderate apraxic

in months. Now as all know...that's not reality with therapy alone.

Anyway -hope I helped and BRAVO!!! to you and !!! You must be over the moon

thrilled with progress Sharon!!! Is your husband still a skeptic? (you don't

say in the blog update)

Sharon's blog for : http://apraxiastory.wordpress.com/before-after-video

Sharon's first testimony for on Pursuit

http://pursuitofresearch.org/testimonials.html

=====

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Hi Sharon,

Thanks for your post! It is inspiring and hopeful to see!

Miner has been on fish oils (Nordic Jr. 3-6-9) for about 4 weeks and NV for

2 weeks and has had a speech therapist coming once a week for 5 weeks now.

I have noticed more " noise " coming from him, but no real improvement in his

speech/communication. He points and says " ehh " a lot to get what he wants

or acts things out. We do have one syllable and some repeat one syllable

word cards we do with him. He can sit and say most of them with me and we

do it daily (probably 25 different words) He makes no attempt to use words

to communicate besides when I sit down with the cards. He only says mom,

dad, me and uice for juice on his own without prompting. I was hoping to

see some more progress, but am trying to have more patience!

I have not been able to find a PROMPT certified therapist in my area. I am

still looking. Some say they are " familiar " with it but not certified. (I

did contact the institute and was given a list... most went to a course, but

aren't certiified..)

I am open to other suggestions on what to try! I was wondering the

difference between the Nordic JR 3-6-9 and the PROEFA/ EPA oils?

Miner is 33 months.

Thanks again for your inspiring videos and information!

Malinda

>

> Wow Sharon both to the surges and to the job you have done in documenting this

journey. Most who are not parents or professionals that deal with apraxia won't

be as impressed by the dramatic surges because most don't appreciate what a

long, slow, intensive speech therapy almost daily road to see even a glimmer of

progress road apraxia typically is. The average person would be more moved by

an older child or teen as they probably look at this and think " cute " but think

he's just " talking like a baby " You see for most -it goes from " he's just a

late talker " to " what's wrong with him " by around the age of 4 years old. I

think you just may be able to skip the horrible stage I and many of us had to go

through -the " what's wrong with him? " stage where perfect strangers believe it

appropriate to ask you that question in public and right in front of your

precious child!!

>

>

> Not only is this remarkable what you did -but even for the public that is

still cluelesss -I think this will be one of the greatest ways to bring

awareness to just what we as parents go through in raising an apraxic child -how

we have to translate for them, and we can. It also shows not all that can't

talk are autistic. clearly is not autistic but clearly is speech impaired

and desperately is trying to talk to you. And by the way Missy -you missed your

calling as a teacher -OMG you are so amazing!!!

>

> These videos bring to light all the times when Tanner was little where he

would talk and people would look at me (his translator :)

>

> And once again if apraxia had physical characteristics...for sure it means

ultra adorable!!!! What a cutie pie!!!

>

> Before I go into my observations just wanted to point out a few technical

difficulties I had because I don't know if it was just my computer. The video

under 2 weeks after nutriiveda where is wearing the white shirt (second one

down there) it starts and stops -so either it's my computer or it's not loaded

right.

>

> Also the video under 3 months -also the second one down -where is singing

" you are my sunshine " I recall that being longer than a sentence -did it get cut

short or did you cut it short?

>

> Also just want to point out that CHERAB is with an 'A' (for apraxia) because

you have it with a U :)

>

> My observations

>

> 1. While I rarely understood him in previous videos without your help or

visual cues -his speech and articulation...OMG what a tremendous difference!!!

>

> 2. Because you don't clarify what's what I have no idea if the surge is from

nutriiveda or the other new thing you just added as you don't really specify how

long and what exactly you are doing with it. To see that tremendous of a surge

in a few months is just amazing. I think you need to break down exactly what

created what surge. I typically waited at least 3 months before adding new

therapies so new and could explain what surges were from what therapies. The

way the blog is now if I was to read it for the first time I'd be a bit

overwhelmed in knowing what to do- what helped the most. In fact based on the

progression it appears since the 6 month update is the most dramatic and recent

that it may have to do with NAET treatments (never did them with Tanner so

unknown to me) How many did you do? I find the fish oils (the essential fatty

acids) to compliment the essential amino acids because both are essential

nutrients. You say the NAET compliments nutriiveda -what is it and how? It

would be good if you can break this down a bit more as again it's hard to know

why he surged so much again between 3 and 6 months and based on what you wrote

it looks like it's the combination...but would he have surged without NAET?

>

> What if....now this is just a thought but I love to do this when people credit

other therapies to surges and I have done this for years with the fish

oils...you keep doing NAET...but stop the nutriiveda for a few days and document

that via video update. To me right now that is the only way of knowing what is

doing what as again it's not clear.

>

> No matter what 's articulation, ability to correct himself when you ask,

talk on command -that's all just amazing.

>

> My suggestion other than trying to stop nutriiveda and just using this other

new thing for a few days...is to teach how to use his toys to motor plan.

From 3 years old I had Tanner using either his hands- or two toys to motor plan

words that he didn't know how to say. is talking so much and from what I

was taught by his SLPs over the years you don't want to get things into the

motor memory wrong -and it appears like with the word " tree " that says it

the way he does because it's in his motor memory that way -so comfortable. But

if he/you were to take one tree and hold it up and say " t " " t " " t " (3 times is

the magic amount I've been told) and then take another tree and hold it up and

say " ree " " ree " " ree " and have him repeat..;then take the one tree he is holding

-the " t " tree and say " t " and the " ree " tree and slowly move them together

saying as they got closer and closer " t " " ree " " t " " ree " and then saying " tree "

that is the way we taught Tanner how to correct.

>

> I was extremely impressed with his alphabet and to me it appears he is working

extra hard in making sure his articulation for the letters was perfect.

>

> Sharon once again this website and all you have done is just incredible and

beautiful. Please don't think I'm being hard on you by pointing out anything

-and please feel free to change or not change based on what you think is best.

I used to be an art director and worked in media and the film industry and I

myself LOVE constructive criticism as that's how we can learn to improve. I

used to hate when someone would look at something I did and just say " wow that's

great " I'd always say " well what can be improved? "

>

> Funniest was one day someone said to me " you always say you love constructive

criticism. What's the difference between criticism and constructive criticism? "

>

> :)

>

> My answer and this is a for real quote

>

> :)

>

> " Criticism is when someone says 'you suck' and constructive criticism is when

someone says 'you suck because' "

>

>

> Anyway in conclusion to add one more thing -I'd have a written evaluation from

your child's SLP included on this page. All of it right now is parental

anecdotal and what we can see -your child's SLP will be awesome in providing a

professional look at what's going on.

>

> I just heard from Barbara SLP yesterday about a parent who took her

child off nutriiveda after a few months and didn't tell her- but the child had a

complete regression in both behavior and speech -ability to imitate etc.

Barbara specifically asked " did you give him his nutriiveda? " and that is when

she found out the parents took the child off for a few days to see if it still

made a difference (did) so of course put him back on and within one day he had

tremendous surges back again. Barbara is thinking of writing a case study on

this. That's what I mean -if your child's SLP is able to write something

up...just like I posted there is going to be a written report from a neurologist

from Kent University where the doctor and SLP both credit nutriiveda (and

therapy of course too) to the child going from profound to mild/moderate apraxic

in months. Now as all know...that's not reality with therapy alone.

>

> Anyway -hope I helped and BRAVO!!! to you and !!! You must be over the

moon thrilled with progress Sharon!!! Is your husband still a skeptic? (you

don't say in the blog update)

>

>

> Sharon's blog for : http://apraxiastory.wordpress.com/before-after-video

> Sharon's first testimony for on Pursuit

http://pursuitofresearch.org/testimonials.html

>

> =====

>

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Sharon-

What is NAET treatments?

[ ] New video after 6mos on

NutriiVeda

Hello all:

I started videoing my son before/after NutriiVeda. Originally, I

posted updates on his before footage, then after 2 weeks on NV, then

after 3 months on NV, and I now have footage of him after 6 months on

NutriiVeda.

In a nutshell, we're still seeing progress. We also did NAET

treatments since the 3mo video update, as he suffers with several

significant IgG & IgG food allergies. Our hope was to remove the

sensitivies/allergies so his body could perform even better with

NutriiVeda. And, I believe it has helped even more. I've got all the

details and video footage on my blog if you'd like to check it out.

Direct link:

http://apraxiastory.wordpress.com/before-after-video/

Once there, you can watch his progression from 27 mos up to the

recent update mentioned above. Or...if you've seen the other video's,

feel free to scroll to the bottom. The last 2 video's are most recent.

Thinking hopeful thoughts for all... :)

sharon

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All:

Thanks for the kind comments on our blog and our son's progress. He is doing

just beautifully. Wanted to respond to a few questions & comments received so

far:

1. Video Technical Difficulties: A couple of the videos aren't working

correctly, but there are still enough to get a good idea of 's progress.

I'm working on this issue now and hope to have it resolved soon.

2. Seems the biggest progress is the most recent video I posted. You can

really start to understand !! lisa asked if my husband was still a NV

skeptic and I'd like to answer that with a big fat NO! He stopped being a

skeptic after the first 2 weeks and doesn't let us leave home without it. He

even takes it as a protein supplement daily - and took even more while he was

training for the 70.3 Ironman competition.

3. NAET: I just want to clarify that we did this therapy specifically to

address 's allergy situation, not to affect his speech/lang per se. While I

know not everyone believes allergies contribute to the performance of our kids

neurologically, there are those who think otherwise (Healing the New Childhood

Epidemics book - Bock). has several significant allergies (IgE)

and the majority are to wheat, milk, barley, etc - essentially gluten and

casein. I did not want to be forced to go completely GFCF - selfish I know, but

true :) So, we were trying to find alternatives. NAET is a VERY alternative

method that is not supported by the traditional medical community and there is

no clinical proof out there that it works. Admittedly, there are probably a

bunch of quacks out there doing it (we even call it " Voo doo " treatments at our

house b/c it's just a very different way of thinking about the body than I'm

used to). However, we were desparate to try to find ways to relieve 's

allergies w/o removing major food groups from his diet. We found a great doc

here locally, Dr Pitman (chiropractor), and saw good results....mostly

specific to 's appetite and willingness to try new foods. NAET is basically

accupressure that targets certain spots in the body to remove the blockage of

energy pathways. It is supposed to remove or lessen the bodies response to an

allergen so it can tolerate a particular food more easily. We go in, they do

accupressure and we have to avoid a specific food for 25 hours - then is

supposedly okay to eat it. I can't know for sure if it is " working " on his

allergies, but we believe we've seen some positive things. I certainly don't

want to give the impression that if you pair NAET with NV you'll see even better

results. They are totally separate in my mind. I originally said they

" complimented " each other b/c, IF eventually we learn it's true that certain

types of allergic/sensitivity responses do affect a more neuro-sensitive child,

then it would make sense that it may allow NV to go deeper for some. I am

nowhere close to being in the medical community, so take this as one mom's

personal theory that I realize is not widely accepted. For now, my family is

100% sold on the surges we're seeing being due to NutriiVeda. The blog you guys

visited is our personal blog dedicated to documenting our journey with apraxia

and all the things we've tried to help him - the good (NV), bad (nothing yet)

and even the wierd (NAET) :)

Sharon

>

> Sharon-

> What is NAET treatments?

>

>

> [ ] New video after 6mos on

> NutriiVeda

>

>

>

>

> Hello all:

>

> I started videoing my son before/after NutriiVeda. Originally, I

> posted updates on his before footage, then after 2 weeks on NV, then

> after 3 months on NV, and I now have footage of him after 6 months on

> NutriiVeda.

>

> In a nutshell, we're still seeing progress. We also did NAET

> treatments since the 3mo video update, as he suffers with several

> significant IgG & IgG food allergies. Our hope was to remove the

> sensitivies/allergies so his body could perform even better with

> NutriiVeda. And, I believe it has helped even more. I've got all the

> details and video footage on my blog if you'd like to check it out.

>

> Direct link:

> http://apraxiastory.wordpress.com/before-after-video/

>

> Once there, you can watch his progression from 27 mos up to the

> recent update mentioned above. Or...if you've seen the other video's,

> feel free to scroll to the bottom. The last 2 video's are most recent.

>

> Thinking hopeful thoughts for all... :)

>

> sharon

>

>

>

>

>

>

>

>

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As a parent who has severe allergies in the family you write this is about NV

but the page ends up being more about what I consider to be a potentially

dangerous allergy method I never heard of which from what I read online is a

scam. Allergies can be life threatening and a child can go into anaphylactic

shock from a food allergy because some parent through their child was cured of

an allergy due to this as you do. You should check with an attorney if you

could be named in a suit if that happened. Sorry if this comes across like I am

upset, I know you should not write when you are upset but my son's pediatrician

and therapist have both approved NV for my son who does have food allergies and

I am scared for parents that don't know reading about this allergy method to

" reset energy pathways " and you do put the two together. You say below you

don't see them together but the following is from your website. Kate

NAET is supposed to de-sensitize or remove your allergies/sensitivities.

Basically, it is a form of accupressure that is supposed to reset the energy

pathways in your body so it can process food and not attack it as an allergen.

" Sounds like voo doo, but given had real milk allergies, etc, we wanted to

try something that wouldn't limit his food intake (and my already less than

impressive cooking abilites). So far, we think it's working and is a really

nice compliment to the work NutriiVeda is doing for him as well. We've done 15

accupressure/NAET treatments so far and after the 2nd one, which was

dairy/calcium, we noticed another surge in appetite, willingness to try new

foods and language/articulation. It's hard to know what's what, but I am still

convinced that NutriiVeda is continuing to allow to progress. I think the

NAET compliments NutriiVeda in that it's letting his body process food easier

and really letting NutriiVeda get in there and do it's best work.

> >

> > Sharon-

> > What is NAET treatments?

> >

> >

> > [ ] New video after 6mos on

> > NutriiVeda

> >

> >

> >

> >

> > Hello all:

> >

> > I started videoing my son before/after NutriiVeda. Originally, I

> > posted updates on his before footage, then after 2 weeks on NV, then

> > after 3 months on NV, and I now have footage of him after 6 months on

> > NutriiVeda.

> >

> > In a nutshell, we're still seeing progress. We also did NAET

> > treatments since the 3mo video update, as he suffers with several

> > significant IgG & IgG food allergies. Our hope was to remove the

> > sensitivies/allergies so his body could perform even better with

> > NutriiVeda. And, I believe it has helped even more. I've got all the

> > details and video footage on my blog if you'd like to check it out.

> >

> > Direct link:

> > http://apraxiastory.wordpress.com/before-after-video/

> >

> > Once there, you can watch his progression from 27 mos up to the

> > recent update mentioned above. Or...if you've seen the other video's,

> > feel free to scroll to the bottom. The last 2 video's are most recent.

> >

> > Thinking hopeful thoughts for all... :)

> >

> > sharon

> >

> >

> >

> >

> >

> >

> >

> >

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I think that she made it very clear that this was something that she was

not sure of, that it was VERY alternative, and I think that she made it

clear that it isn't for everyone. I too have a child with allergies,

some severe, and I like to hear about potential therapies.... two years

ago if someone told you to give your child a protein shake to make them

talk you might have thought that was crazy...

In addition, the Nutrition Genius that everyone was jumping all over the

other day is very nice. I had a response from him about some questions

and he is like all of the others out here..... in the same boat, but

very willing to help.

Please try not to come down so much on these posters.... you haven't met

with the doctor she uses and spoke with him about this have you? We are

all under the same pressures, and I feel like any parent with severe

allergies that knows their child will understand what they are capable

of eating...

Also, these IgEs can be caused from food allergies that aren't life

threatening, such as with my daughter. She has over 15 foods that cause

spikes in her blood, but no real outward signs... wheezing, hives,

shock....

Sharon, thank you for sharing, as I was the one who was curious about

the treatment, and I appreciate you taking the time to write back.

Lets not attack each other on here....

[ ] New video after 6mos on

> > NutriiVeda

> >

> >

> >

> >

> > Hello all:

> >

> > I started videoing my son before/after NutriiVeda.

Originally, I

> > posted updates on his before footage, then after 2 weeks on

NV, then

> > after 3 months on NV, and I now have footage of him after 6

months on

> > NutriiVeda.

> >

> > In a nutshell, we're still seeing progress. We also did NAET

> > treatments since the 3mo video update, as he suffers with

several

> > significant IgG & IgG food allergies. Our hope was to remove

the

> > sensitivies/allergies so his body could perform even better

with

> > NutriiVeda. And, I believe it has helped even more. I've got

all the

> > details and video footage on my blog if you'd like to check

it out.

> >

> > Direct link:

> > http://apraxiastory.wordpress.com/before-after-video/

> >

> > Once there, you can watch his progression from 27 mos up to

the

> > recent update mentioned above. Or...if you've seen the other

video's,

> > feel free to scroll to the bottom. The last 2 video's are

most recent.

> >

> > Thinking hopeful thoughts for all... :)

> >

> > sharon

> >

> >

> >

> >

> >

> >

> >

> >

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Kate:

I apprecite your response and, while doesn't have life threatening

allergies, I can only imagine the fear and worry it might create when reading

something like this.

While I certainly don't want to start a posting war (as I know your note was

meant that way) :), I wanted to at least respond.

I have been a member of this messageboard for well over a year now and consider

it to be a place where we all share what is going on with our kids/families -

the good, the bad, the ugly and even the wierd. That's all I was doing -

sharing my personal experience. I was not making a recommendation for others to

try NAET in any way.

In regards to it being a scam...who knows. I know what I and my son experienced

with it, and we are pleased. As well, I researched this for over a year before

we tried it, and was encouraged by some truly great people whom I trust. I'll

be the first to admit it sounds odd, but to be fair, if you google Chelation,

Cranial Sacral therapy or even NutriiVeda, there's plenty of sites (on the first

page of google even) that call them out as scams as well. I think we can ALL

agree that NV is not a scam, and although I haven't tried cranial sacral therapy

or Chelation, I know many many parents on this messageboard (and personally) who

swear it's been an integral part of their child's progress.

I saw a note come through the messageboards asking what NAET was, so I clarified

further in my note earlier today - because I was asked to. It is quite simply

accupressure (which is very similar to accupuncture). I tried to make it clear

in my note that it is not a widely accepted form of therapy by saying:

" NAET is a VERY alternative method that is not supported by the traditional

medical community and there is no clinical proof out there that it works.

Admittedly, there are probably a bunch of quacks out there doing it (we even

call it " Voo doo " treatments at our house b/c it's just a very different way of

thinking about the body than I'm used to). "

and went on to clarify that I'm not in the medical field and it's just my

personal experience as a Mom. I would hope that someone wouldn't read one

messageboard post and run out and do ANYTHING without further research and then

sue me if it didn't work out.

I am really sorry that I offended you, as that was far far from my intention. I

truly just wanted to share the total story of what's happened with my son in the

last 3 months since we posted, and felt it wasn't fair to not include a therapy

we had tried. I will say it again, we still believe NV is THE biggest factor in

my son's progress in the last 6 months, but I stand by what I wrote about NAET

earlier, as it was just a simple, sincere effort to share a personal story.

All the best,

Sharon

> > >

> > > Sharon-

> > > What is NAET treatments?

> > >

> > >

> > > [ ] New video after 6mos on

> > > NutriiVeda

> > >

> > >

> > >

> > >

> > > Hello all:

> > >

> > > I started videoing my son before/after NutriiVeda. Originally, I

> > > posted updates on his before footage, then after 2 weeks on NV, then

> > > after 3 months on NV, and I now have footage of him after 6 months on

> > > NutriiVeda.

> > >

> > > In a nutshell, we're still seeing progress. We also did NAET

> > > treatments since the 3mo video update, as he suffers with several

> > > significant IgG & IgG food allergies. Our hope was to remove the

> > > sensitivies/allergies so his body could perform even better with

> > > NutriiVeda. And, I believe it has helped even more. I've got all the

> > > details and video footage on my blog if you'd like to check it out.

> > >

> > > Direct link:

> > > http://apraxiastory.wordpress.com/before-after-video/

> > >

> > > Once there, you can watch his progression from 27 mos up to the

> > > recent update mentioned above. Or...if you've seen the other video's,

> > > feel free to scroll to the bottom. The last 2 video's are most recent.

> > >

> > > Thinking hopeful thoughts for all... :)

> > >

> > > sharon

> > >

> > >

> > >

> > >

> > >

> > >

> > >

> > >

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It's tough sometimes via email for passionate and loving parents to share and

not be attacked by others for doing so by others. And it happens on both sides

of the fence. Vaccines for example are very rarely brought up without both

sides jumping in...however what caught my eye on one debate was a parent on the

pro flu vaccine side wrote about the death of a child she knew, and the anti flu

vaccine side posters just continued on attacking without noticing (literally)

the dead body that was now in the middle of the debate.

What we all should remember is that if we all met in person it would be more

unlikely these type of debates would happen because most just read the words and

forget there are real people behind them who are going through real life

struggles. Most of are members are either parents or professionals that deal

directly on a daily basis with at least one special needs child.

I've tried to search the archives to find out more about this debate but there

is very little info in our archives on naet -so unlike vaccines this isn't a

well known debate at least here. Like Sharon I have tried many therapies over

the years to try to help, but unlike Sharon my children don't have any allergies

so can't really comment on this approach. What I typically look for is

alternative therapies that are benign, and affordable...if you want to try

letting your child swim with a dolphin, sleep with a magnet under his pillow,

try any of the sensory therapies, music, listening, etc. that's fine.

From what I understand ASHA doesn't respect oral motor therapy which I find to

be nuts, and don't you worry about apraxia because I remember when we first ran

our support meetings there were a group of SLPs arguing at one of our first

meetings about the existence of apraxia as some of the SLPs thought it was a

scam concocted by certain SLPs to make more money from parents for increased

speech therapy...but when a medical doctor uses off label medications with

unknown and known severe side effects to try to treat autism outside of the

realm of a clinical study...would that be a scam? Or would that just fall under

dangerous. I mean there is a difference to me between a waste of money and a

risk of someone's life. And how in the world is electroshock therapy back in

vogue again?

I mean we can fight amongst ourselves but we need to look at the bigger picture

I believe. We have a rising group of children for still an unknown reason who

have various amounts of neurologically based impairments to communication, motor

planning, muscle tone, sensory issues...and add to that those that have severe

psychological issues on top of the impairments. Some call all of it autism -but

autism doesn't come with a clear list of therapies that are good and bad

depending upon the diagnosis -so your child gets the diagnosis of autism and

your child is not autistic your child probably gets therapy and placement that

is inappropriate.

But going back to what does this large group mean? It means that we can fight

amongst ourselves or continue to love our children while keeping an eye on the

big picture. Kate you said so yourself that you know about allergies so someone

like you that has a child or family history of severe allergies is probably not

going to try to cure an allergy the way Sharon did...but keep in mind in regards

to over diagnosis, in my opinion some alternative professionals recommend trying

a trial of dairy elimination as an auto response...which in direct response to

that according to the research there is now a rise in children with short

statue, weak brittle easy to break bones, and for some reason prone to obesity.

What does that tell me -as always most don't look at the pros and the cons as

there are both sides to just about everything.

I am from the school of thought to study what you are going to try, consult with

medical professionals you respect, and for me I only tried things again that

were benign...well if you consider having electrodes attached to your face to

try to stimulate the nerve endings from oral apraxia benign!! Yes I had to do

it before Tanner would even try it.

I have tried various therapies but through the years the only consistent have

been traditional speech therapy from at least one or more therapist that I

trust, fish oils, appropriate placement...and that's pretty much the past

decade. As I write all the alternatives in The Late Talker book I left enough

time in between each to know what did what. Tanner has been on nutriiveda

steady since October of 2009 and I have written here over the past few months

the various surges I have seen in my son which are unexplainable other than to

the nutriiveda as we are not doing anything else new and the kid just turned 14-

we had started to accept his little quirks from apraxia as " Tanner " I mean was

he mainstreamed, talking, friends with lots of other kids, a good student? Yes

all of the above...but if you look at this list here

http://pursuitofresearch.org/pursuit.html

SPEECH articulation, complexity and sophistication of sentence structure

LANGUAGE better understanding of written and spoken word, development of

better reading and writing skills

ACADEMICS/LEARNING reported surges in all areas of school

FINE AND GROSS MOTOR SKILLS also multi tasking

SENSE OF HUMOR both catching subtle humor and wanting to make others

laugh-joking around

AWARENESS OF SURROUNDINGS (for autism) reported following gaze and more

interactions

FACIAL EXPRESSIONS more non-verbal communication, for oral apraxia more

expressions instead of blank stares when not engaged in conversation

FOCUS on task, more willing to listen and try

MULTI TASKING (for apraxia as this is something typically not done or done

well)

SOCIAL wanting to participate with others via play and communication

MOOD reported seems " happier " for a number

DEVELOPMENTAL CATCHING UP for those that never went through stages

-reportedly going through them for the first time.

DECREASE IN SEIZURES so far in several cases elimination of any seizures and

headaches and decrease in seizure meds as well

IMAGINATIVE PLAY increase in imaginative play and story telling

Within 1 month or more:

SENSORY improvement in sensory awareness for those affected with sensory

integration dysfunction

GROWTH reported dramatic surges in height as well as increase in muscle and

normalization in weight

Much of the above were first seen firsthand by me in my son Tanner and since

then reported by others, and more amazing -typically for some reason more so by

professionals that work with the child rather than the parent.

I don't really know any risks to trying cranial sacral or any massage for a

normal person. I don't know of any risks at all of trying nutriiveda and in

fact in my opinion there are risks from feeding your child most of the food out

there...but I do know there are risks to chelation so I wouldn't put that in the

same boat as a benign therapy. Kate feels there is a risk to naet but in my

opinion again I highly doubt anyone who has a child with a severe allergy will

go full steam ahead without their doctor into this.

So again to me this is about yes being able to share, but also knowing that just

because something is recommended by a traditional speech therapist or medical

doctor doesn't mean it's fine automatically either. Dig, ask questions, open

new doors, explore pros and cons. That's what this group should help with.

=====

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OMG! In my note below tht just passed through, I meant to say

" as I know your note was NOT meant that way " - not that it was.

Sorry for the typo - was typing fast and missed a VERY important word of that

sentence.

> > > >

> > > > Sharon-

> > > > What is NAET treatments?

> > > >

> > > >

> > > > [ ] New video after 6mos on

> > > > NutriiVeda

> > > >

> > > >

> > > >

> > > >

> > > > Hello all:

> > > >

> > > > I started videoing my son before/after NutriiVeda. Originally, I

> > > > posted updates on his before footage, then after 2 weeks on NV, then

> > > > after 3 months on NV, and I now have footage of him after 6 months on

> > > > NutriiVeda.

> > > >

> > > > In a nutshell, we're still seeing progress. We also did NAET

> > > > treatments since the 3mo video update, as he suffers with several

> > > > significant IgG & IgG food allergies. Our hope was to remove the

> > > > sensitivies/allergies so his body could perform even better with

> > > > NutriiVeda. And, I believe it has helped even more. I've got all the

> > > > details and video footage on my blog if you'd like to check it out.

> > > >

> > > > Direct link:

> > > > http://apraxiastory.wordpress.com/before-after-video/

> > > >

> > > > Once there, you can watch his progression from 27 mos up to the

> > > > recent update mentioned above. Or...if you've seen the other video's,

> > > > feel free to scroll to the bottom. The last 2 video's are most recent.

> > > >

> > > > Thinking hopeful thoughts for all... :)

> > > >

> > > > sharon

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

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