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Barbara,

I'm wondering if you have any info on how Nutriveda might affect kids with

seizures. Also, do you know what the carbohydrate content is?

Thanks!

Tamsin (mom to Lulu with seizures on ketogenic diet)

________________________________

From: Barbara <helpmespeak@...>

Sent: Wed, January 13, 2010 2:50:44 PM

Subject: [ ] NutriiVeda amount

There are 2 canisters per order; each has 30 scoops of Nutriiveda powder;

an adult dose (9yrs+>)= 2scoops/ once or twice a day

a 4-8yo= 2scoops/day

a child <4yrs = 1 scoop/day

Once a day is recommended for nutrition and maintenance and twice a day for for

weight loss and/or for those that don't need more of the nutrients. So an adult

could use any range from 2 to 4 cans/month and kids under 9 can range from 1 to

2 cans a month.

Call my cell 410-274-9898 or office (M-Th 9-8) with any additional

questions.

Warmest wishes,

Barbara

Barbara A. , M.S., CCC-SLP

Executive Director/ Help Me Speak, LLC

<http://www.helpmesp eak.com/> http://www.helpmesp eak.com

(o) 410-442-9791 (f) 410-442-9783

2500 Wallington Way; Suite 103

Marriottsville, MD 21104

follow us on FaceBook:

http://www.facebook .com/pages/ Marriottsville- MD/Help-Me- Speak-LLC/

1046288520

32

From: @groups. com

[mailto: @groups. com] On Behalf Of tgowest

Sent: Wednesday, January 13, 2010 8:21 AM

@groups. com

Subject: [childrensapraxiane t] Re: Update on Tanner on

Nutriiveda/interest ingnew study

How long does the $87.50 container last? Is it a couple of months?

>

> It's $87.50 (incl tax & sh) You can find it at

http://www.pursuito fresearch. org Contact me if you have any questions

>

> Warmest wishes,

>

> Barbara A , M.S., CCC-SLP

> Executive Director, Help Me Speak, LLC

> 410-442-9791

>

>

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Until Barbara answers -I know that Ketchum (see

http://www.pursuitofresearch.org under blogs) was in the hospital about 4 years

ago and 2 years ago almost died from seizures and has been not only seizure free

since on the nutriiveda but her doctor has just lowered the Depakape dosage

because of how well Mel is doing. She's also no longer getting headaches, no

eyes tearing up from head pain, no staring spells, not getting stuck in her

movement, and due to privacy issues can't say why -but for sure no more seizures

through the night either.

Mel had sadly gained 30 pounds on the Depakape but since being on the Nutriiveda

this past month she lost 10 pounds (!!!) Not that Robin brings this up in the

blog yet -but this is in addition to all the other amazing surges -like

outgrowing her computer program. I'm sure Robin will update more.

As a matter of fact Robin had told me that while she was taking care of a friend

who has cancer Tom was taking care of Mel and thought Mel only got 2 scoops a

day (which is what Mel's sisters take) Well Mel regressed -just like Tanner she

had trouble once again with feeding herself with the spoon again, no normal

babble or speech again, no smiling -just a blank face- not caring if she just

sat and watched TV. Robin put her back on 4 scoops a day yesterday and she woke

up today all " chattery " again today as she had been before. So just like my son

the regression is THAT quick off of it.

If you want to see the ingredient list check here

You can find tons of info on it at http://www.pursuitofresearch.org under Zrii

product under nutriiveda. (exact page is

http://pursuitofresearch.hmgsuccess.com/?page_id=392 )

Here's nutrition label for chocolate

http://www.up0.net/content/666799/Choco_NutritionFacts.pdf

and vanilla

http://www.up0.net/content/666799/Vanilla_NutritionFacts.pdf

Again I'm sure you'll hear more from Barbara and Robin!

Also Robin wants to update about her daughter Tomi -which is an amazing

testimony for athletes- and there are doctor reports behind this too.

(Robin said she's starting to share at Big Tent too!

https://www.bigtent.com/groups/cherab )

=====

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For those of you who have their children on Nutriiveda, did you take them off of

their regular multi-vitamins? I assume you've continued with the Omegas?

From: kiddietalk@...

Date: Wed, 13 Jan 2010 23:38:36 +0000

Subject: [ ] Re: NutriiVeda amount

Until Barbara answers -I know that Ketchum (see

http://www.pursuitofresearch.org under blogs) was in the hospital about 4 years

ago and 2 years ago almost died from seizures and has been not only seizure free

since on the nutriiveda but her doctor has just lowered the Depakape dosage

because of how well Mel is doing. She's also no longer getting headaches, no

eyes tearing up from head pain, no staring spells, not getting stuck in her

movement, and due to privacy issues can't say why -but for sure no more seizures

through the night either.

Mel had sadly gained 30 pounds on the Depakape but since being on the Nutriiveda

this past month she lost 10 pounds (!!!) Not that Robin brings this up in the

blog yet -but this is in addition to all the other amazing surges -like

outgrowing her computer program. I'm sure Robin will update more.

As a matter of fact Robin had told me that while she was taking care of a friend

who has cancer Tom was taking care of Mel and thought Mel only got 2 scoops a

day (which is what Mel's sisters take) Well Mel regressed -just like Tanner she

had trouble once again with feeding herself with the spoon again, no normal

babble or speech again, no smiling -just a blank face- not caring if she just

sat and watched TV. Robin put her back on 4 scoops a day yesterday and she woke

up today all " chattery " again today as she had been before. So just like my son

the regression is THAT quick off of it.

If you want to see the ingredient list check here

You can find tons of info on it at http://www.pursuitofresearch.org under Zrii

product under nutriiveda. (exact page is

http://pursuitofresearch.hmgsuccess.com/?page_id=392 )

Here's nutrition label for chocolate

http://www.up0.net/content/666799/Choco_NutritionFacts.pdf

and vanilla

http://www.up0.net/content/666799/Vanilla_NutritionFacts.pdf

Again I'm sure you'll hear more from Barbara and Robin!

Also Robin wants to update about her daughter Tomi -which is an amazing

testimony for athletes- and there are doctor reports behind this too.

(Robin said she's starting to share at Big Tent too!

https://www.bigtent.com/groups/cherab )

=====

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Just wanted to clarify on this due to an email I got!!! No Tanner never had

trouble feeding himself -at least as long as I can remember. Tanner did regress

twice when not on the nutriiveda- but for him it shows as hesitations in speech

-or what I call " bumpy " . He wasn't off it more than a weekend the second time

-but the regression is quick off it or even when reduced to once a day (2

scoops) just like Mel. But right away surges once back on...It does appear that

there is a link to the fish oils in that the surges and regressions are so

quick.

So I meant to say like ; on just one dosage a day (2 scoops) Tanner

regresses for some reason...and when put back on the 2 dosages (4 scoops a day)

Tanner surges again. Like Mel he did have a dramatic change in facial

expressions since being on this. Tanner has oral apraxia and while he's been

mainstreamed and is a good student -the lack of facial expressions for those

that don't know him make it appear as if he's not paying attention. Like Robin

said it's a " blank look " As I've posted Tanner's surges are not limited to just

speech and facial expressions but reading, school, energy, focus, sense of

humor...and even interests! I mean he all of a sudden is interested in Japanese

movies with subtitles and is apparently starting to learn some Japanese from

watching...Dakota is the one that noticed that new interest.

But most just notice the change in speech and facial expressions to start.

Since the nutriiveda Tanner as some of you have seen in person or through

photos- has facial expressions all the time now (Yay!!!!) and his speech and

communication as well as even interests appear to have become more sophisticated

and quick. Just amazing.

I'm not sure why some of our kids regress on just one serving (2 scoops) vs the

4 scoops a day. I'm not suggesting that little ones need to be on a higher

dosage, and we are getting reports of surges on the lower dosages for little

ones -but just want to point out we still don't know what is creating the

surges. Do we need a particular dosage of it? Or is it the synergistic blend?

Right now we don't know.

One of the parents I was speaking with today said to me " what would you do if

they stopped making it? " The thought honestly makes me sick to my stomach. You

know what my husband said when I said this to him? " I would take a canister of

it to a lab and have them make it up for me. Regardless of the cost we can't

have our children regress " Wow! And this coming from Glenn who when I first

started this with Tanner he was SO skeptical! ha- funny. I mean they say

lightning doesn't strike twice -but after having 2 kids with special needs- go

figure that I would be the voice to not just fish oil for our kids....but now

" chocolate milk " as my husband calls it too. This time I found out by mistake.

Who would have ever thought??? Then again they say the greatest things happen

by mistake.

And PS -Nelia just saw your question and yes the nutriiveda is full meal and

vitamin replacement if you want it to be. (please see nutritional info in links

I've sent out) No vitamins anymore but I didn't and wouldn't stop the fish oils

-but that's me. But I did cut Tanner's dosage in half.

=====

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Thanks ,

That's exactly the information I was looking for.

Tamsin

________________________________

From: kiddietalk <kiddietalk@...>

Sent: Wed, January 13, 2010 7:55:28 PM

Subject: [ ] Re: NutriiVeda amount

Just wanted to clarify on this due to an email I got!!! No Tanner never had

trouble feeding himself -at least as long as I can remember. Tanner did regress

twice when not on the nutriiveda- but for him it shows as hesitations in speech

-or what I call " bumpy " . He wasn't off it more than a weekend the second time

-but the regression is quick off it or even when reduced to once a day (2

scoops) just like Mel. But right away surges once back on...It does appear that

there is a link to the fish oils in that the surges and regressions are so

quick.

So I meant to say like ; on just one dosage a day (2 scoops) Tanner

regresses for some reason...and when put back on the 2 dosages (4 scoops a day)

Tanner surges again. Like Mel he did have a dramatic change in facial

expressions since being on this. Tanner has oral apraxia and while he's been

mainstreamed and is a good student -the lack of facial expressions for those

that don't know him make it appear as if he's not paying attention. Like Robin

said it's a " blank look " As I've posted Tanner's surges are not limited to just

speech and facial expressions but reading, school, energy, focus, sense of

humor...and even interests! I mean he all of a sudden is interested in Japanese

movies with subtitles and is apparently starting to learn some Japanese from

watching...Dakota is the one that noticed that new interest.

But most just notice the change in speech and facial expressions to start.

Since the nutriiveda Tanner as some of you have seen in person or through

photos- has facial expressions all the time now (Yay!!!!) and his speech and

communication as well as even interests appear to have become more sophisticated

and quick. Just amazing.

I'm not sure why some of our kids regress on just one serving (2 scoops) vs the

4 scoops a day. I'm not suggesting that little ones need to be on a higher

dosage, and we are getting reports of surges on the lower dosages for little

ones -but just want to point out we still don't know what is creating the

surges. Do we need a particular dosage of it? Or is it the synergistic blend?

Right now we don't know.

One of the parents I was speaking with today said to me " what would you do if

they stopped making it? " The thought honestly makes me sick to my stomach. You

know what my husband said when I said this to him? " I would take a canister of

it to a lab and have them make it up for me. Regardless of the cost we can't

have our children regress " Wow! And this coming from Glenn who when I first

started this with Tanner he was SO skeptical! ha- funny. I mean they say

lightning doesn't strike twice -but after having 2 kids with special needs- go

figure that I would be the voice to not just fish oil for our kids....but now

" chocolate milk " as my husband calls it too. This time I found out by mistake.

Who would have ever thought??? Then again they say the greatest things happen

by mistake.

And PS -Nelia just saw your question and yes the nutriiveda is full meal and

vitamin replacement if you want it to be. (please see nutritional info in links

I've sent out) No vitamins anymore but I didn't and wouldn't stop the fish oils

-but that's me. But I did cut Tanner's dosage in half.

=====

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Hi Tamsin,

has had seizures for the past 4 years and now that she is on

the Nutriiveda we have not seen any seizure activity. is

still on medication

for her seizures but her dose has been decreased. feels

better with less seizure medication and has lost 10 pounds so far of

he 20 pounds that she

needed to lose due to her medication. This is the first year we will

be able to travel with and we are all looking forward to some

vacation time.

Please e-mail me if you have any other questions.

Thanks,

Robin

rcketchem@ bellsouth.net

On Jan 13, 2010, at 5:50 PM, Tamsin Eames wrote:

> Barbara,

>

> I'm wondering if you have any info on how Nutriveda might affect

> kids with seizures. Also, do you know what the carbohydrate content

> is?

>

> Thanks!

>

> Tamsin (mom to Lulu with seizures on ketogenic diet)

>

> ________________________________

> From: Barbara <helpmespeak@...>

>

> Sent: Wed, January 13, 2010 2:50:44 PM

> Subject: [ ] NutriiVeda amount

>

> There are 2 canisters per order; each has 30 scoops of Nutriiveda

> powder;

>

> an adult dose (9yrs+>)= 2scoops/ once or twice a day

>

> a 4-8yo= 2scoops/day

>

> a child <4yrs = 1 scoop/day

>

> Once a day is recommended for nutrition and maintenance and twice a

> day for for weight loss and/or for those that don't need more of the

> nutrients. So an adult could use any range from 2 to 4 cans/month

> and kids under 9 can range from 1 to 2 cans a month.

>

> Call my cell 410-274-9898 or office (M-Th 9-8) with any additional

> questions.

>

> Warmest wishes,

>

> Barbara

>

> Barbara A. , M.S., CCC-SLP

>

> Executive Director/ Help Me Speak, LLC

>

> <http://www.helpmesp eak.com/> http://www.helpmesp eak.com

>

> (o) 410-442-9791 (f) 410-442-9783

>

> 2500 Wallington Way; Suite 103

>

> Marriottsville, MD 21104

>

> follow us on FaceBook:

> http://www.facebook .com/pages/ Marriottsville- MD/Help-Me- Speak-

> LLC/ 1046288520

> 32

>

> From: @groups. com

> [mailto: @groups. com] On Behalf Of tgowest

> Sent: Wednesday, January 13, 2010 8:21 AM

> @groups. com

> Subject: [childrensapraxiane t] Re: Update on Tanner on

> Nutriiveda/interest ingnew study

>

> How long does the $87.50 container last? Is it a couple of months?

>

>

> >

> > It's $87.50 (incl tax & sh) You can find it at

> http://www.pursuito fresearch. org Contact me if you have any

> questions

> >

> > Warmest wishes,

> >

> > Barbara A , M.S., CCC-SLP

> > Executive Director, Help Me Speak, LLC

> > 410-442-9791

> >

> >

>

>

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So apparently someone is making A LOT of money on this since it seems it would

take $160 plus shipping and taxes for a one month supply. Too bad not all

families have the finances for this miracle.

> >

> > It's $87.50 (incl tax & sh) You can find it at

> http://www.pursuitofresearch.org Contact me if you have any questions

> >

> > Warmest wishes,

> >

> > Barbara A , M.S., CCC-SLP

> > Executive Director, Help Me Speak, LLC

> > 410-442-9791

> >

> >

>

>

>

>

>

>

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When I first spoke to about Nutriiveda I also had some

reservations concerning the price. I spoke with at length about

all the life changes the Nutriiveda had made for Tanner plus her

family. I decided I wanted to try the Nutriiveda for as a

weight loss option as had gained 30 pounds thanks to her

seizure medication. I spoke with my husband about the Nutriiveda and

all the changes that 's family has experienced and asked him what

he thought. He looked at me and asked me how could I put a price on

's health. He reminded me of all the money we had already

spent on either 's lawsuit, various evaluations by doctors

around the country, and taking her to a variety of therapies each

week. He asked me did I once think of that money we had spent. I had

to answer that I actually had not so he asked me what was the

difference. Wow I thought to myself he was right.

We had a family meeting to discuss beginning Nutriiveda.

Immediately the rest of my family wanted to take the Nutriiveda as

well to show support for . I thought to myself and proposed

this question to my family how are we going to afford for everyone to

take Nutriiveda each day with . Well my family has decided to

make budget cuts in the family budget. This is what we have done to

be able to afford the Nutriiveda. We no longer go to movies we go to

the Red Box instead and have movie night each Saturday night. We no

longer eat out but we still have a special meal each weekend we just

make it at home. We only purchase items that are on sale and we

really think twice before we purchase that item. Our grocery bill has

been cut by 60% as I am purchasing less food and really pay close

attention to the sales. I make up our dinner menu each week now

according to the items that are on sale.

The product is being sold at wholesale cost. The changes that I am seeing

in my entire family no amount of money could ever replace. is

doing so well and thanks to Nutriiveda we have a much different

concern for her this year. We are now worried about communication for

and yes we still worry about seizures for but not as

much. We are able to pursue things this year for that we

never thought was a possibility any longer. has also lost 10

pounds and does not feel the need to eat on a constant basis. She is

much happier these days!! Mindy our middle daughter is working out at

the gym each day and running around the campus. She told my husband

last night that she has never felt so well in her entire life and

thanked us for allowing her to use the Nutriiveda. Tomi our youngest

daughter is now training for the Jr. Olympics once again for long

distance running. That dream was taken away from her over a year ago

and now she is back training thanks to the Nutriiveda repairing her

injuries. We spent 4 days a week in PT for 6 months and had a

Personal Trainer for Tomi so she could run once again and that did not

work. Tomi was told last October by her doctor that he was sorry but

there was nothing else that could be done for her and to look for

another sport that would not be as hard on her legs. Tomi was told

yesterday that her ankles are all healed and her injury is healed as

well. Tomi has her first official race this Saturday and has been

training hard all week without any pain and her time has gotten faster

once again for her running. Tom is losing his weight but more

importantly is able to maintain his work schedule and work his 11 hour

days without feeling exhausted at the end of the day. Tom works a 4

day work week schedule due to the fact that has always had so

many doctor appts. and he did not want to miss one. Now is

going once a month and soon that will be changed to once every 6 weeks

for her seizure checkup. I feel much better and find myself having

the energy to do everything that his now needed to be done each day

due to wanting to explore life and Tomi's training schedule.

I know the Nutriiveda works. I have seen many changes within my own

family. I would continue to cut our budget if necessary to make sure

our family can continue on the Nutriiveda. Please if I can answer any

questions e-mail me at rcketchem@.... I truly believe in

Nutriiveda and see changes within my own family each day. As I type

this e-mail, has either been humming, saying all the words

she knows, or making new sounds without stopping. Last year she was

quiet and had a blank expression and this year many amazing changes.

All this thanks to Nutriiveda!

Robin

On Jan 14, 2010, at 8:24 AM, tgowest wrote:

> So apparently someone is making A LOT of money on this since it

> seems it would take $160 plus shipping and taxes for a one month

> supply. Too bad not all families have the finances for this miracle.

>

>

> > >

> > > It's $87.50 (incl tax & sh) You can find it at

> > http://www.pursuitofresearch.org Contact me if you have any

> questions

> > >

> > > Warmest wishes,

> > >

> > > Barbara A , M.S., CCC-SLP

> > > Executive Director, Help Me Speak, LLC

> > > 410-442-9791

> > >

> > >

> >

> >

> >

> >

> >

> >

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Its very easy to read numbers but very difficult to visualise progress because

progress is an unmeasurable quantity.

My son has double diagnosis. We have tried everything under the roof...ABA, 4x

speech[not PROMPT], OT, TOmatis Litsening Therapy, Hippotherapy, Biomedical,

neurofeedback, chiropractic treatment, accupuncture, NACD.... He still has not

shown any surges...even though he has made progress. When Nutriiveda was first

mentioned I jumped right away because it was something within my territory. I

have known 90% of the ingredients from my childhood.

We cannot afford lots of stuff and it is expensive for us....our household runs

from paycheck to pay check...but we are ready to do anyting to help our son.

Especially when something is ALL NATURAL we are all for it.

There are still no concrete study to say why our kids are like this why they

struggle to communicate, why they are " different " from the rest. No matter what

the reasons are - it has not stopped anyone among us from looking for

answers....looking for that RAY OF LIGHT , THAT HOPE - that things will turn

arround and that you would hear that little sweet voice calling out to you. The

day I hear my son talk in sentences is sure going to be PRICELESS.

sowmya

>

> Dear tgowest,

>

> Just like what is " talking " what is expensive is relative. Each 2 scoops of

nutriiveda which is gluten casein free, fat and sodium free, all natural with 20

grams of isolate protein which is easily digestible per serving with all the

essential amino acids, vitamins and minerals costs about 2.70 per full serving

which is 2 scoops and is FULL meal and vitamin replacement.

>

> We talk about 2 types of people at least that are looking at the product. For

teens and adults that are looking to lose weight with or without apraxia,

autism, ADHD, and for those of all ages little ones to seniors who don't eat

enough or well and no matter how overweight they are they are undernourished and

full of ama (toxins). Many young children and thin healthy people who just want

to supplement and maintain would use just one serving a day to nourish, replace

one meal, and naturally detox the body. And yes you could eat with it or mix it

with food -but it is very filling and you don't have to.

>

> So

> to use it 2x a day @ 2 scoops each so 4 scoops a day = 5.40 a day

> to use it 1x a day @ 2 scoops each so 2 scoops a day = 2.70 a day

> for children under 4 @ 1 scoop a day =1.35 a day

>

> So each serving to put that into overweight average American perspective...

less than the cost of a Happy Meal per serving.

>

> I know Robin said her grocery bill was cut by 60 percent and I know she's not

using it to replace dinner like we are...we are using it to replace dinner and

for less than 3 dollars a person per meal.... we have MORE money in our

household because we are spending WAY less on food, snacks...and even if we do

go out to dinner none of us seem to eat as much! So we are going to movies

more. (Avatar 3D was great!!)

>

> After spending at one point hundreds (and hundreds and hundreds) a WEEK on

private therapy both traditional (even back when Tanner's private SLP was 100

dollars for 1.2 hour) and alternative not excluding cranial sacral,

hippotherapy, or those magnets I stuck under his pillow " just in case " and don't

forget to add the gas and time driving all over the place for therapy- and

should I include my passes to Disney and Universal for my " ride therapy " ??? to

try to seek help for my son Tanner- to me it's remarkably and almost TOO CHEAP

to have the amount of surges we are seeing in a 13 year old for ONLY 160 a

month...and that covers 2 meals a day for him too??? That's like that old

Saturday Night Live skit " it's a dessert topping...and a floor cleaner! " I mean

who would have thought???

>

> And in just a few months as close to normal as ever? = Priceless.

>

> And this isn't only about my son Tanner now -did you actually take the time to

read Robin's blog about her TWENTY FIVE YEAR OLD DAUGHTER who up till...um about

a month ago when she started nutriiveda -was essentially sitting on the coach

watching TV each day, not talking, feeding herself, in pain, on high levels of

seizure meds, in a shell -and now she's seeing the world for the first time...a

child who was misdiagnosed most of her life as mentally retarded and autistic

-who sued the PA school system for abuse and won, who has been to therapists and

doctors and therapy all over the country...perhaps you need to read this again:

> http://littlemermaidmelanie.wordpress.com/about/

>

> And you read that and think...wow she spent " $160 plus shipping and taxes for

(that) one month supply...someone is making a TON of money "

>

> Oh and PS -some of our states don't charge tax- like mine doesn't.

>

> Even though we didn't have to -Cherab sells it wholesale and supports the

Cherab Foundation so you buy it at the exact same cost as if you were a

distributer -but you can buy it retail through the Chopra Center for Wellbeing

and ask Dr. Chopra if he's making a profit.

http://store.chopra.com/productinfo.asp?item=708 I sure hope he is because right

about now I'm ready to build a little shrine in my front yard to him for this

life changing inexpensive remarkable product called nutriiveda. Those who want

to support Cherab can continue to buy it through

http://www.pursuitofresearch.org and the world will know when we are making a

TON of money (which I hope is soon) selling it at our wholesale cost because

then we can get the fish oil study done finally and 'try' to end the

ignorance...but clearly sometimes it will always stick it's ugly head out.

>

> =====

>

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Oh sowmya, isn't that the truth. I'll never forget telling my son's first

speech therapist that if he could just say ma, mom, mommy, mama - I'd be over

the moon with happiness. And I was beyond happy when it happened. AND when he

said Aye O Oooo - for I love you - a hugged him and cried a river of tears

(frightening him in the process!).

My outlook has been from the start - if it might help and it doesn't hurt we'll

give it a shot. This healthy protein powder definitely fits my criteria. LOL -

in fact - it is one better - it is a - it is healthy, it might be helping and it

won't hurt!!

Expensive? Would I buy it for myself for a meal replacement (assuming I wasn't

allergic to dairy)? Maybe yes, maybe no (I'm a mom - my needs are lower on the

priority scale!!). Would I buy it for my son to try as a possible help -

without question or hesitation. Am I glad I took the plunge and bought it for

him and started him on it? Without question! Am I sure that the surges I am

seeing are because of the powder? No. BUT THEY JUST MIGHT BE. Do I plan to

keep him on it? You better believe it. Am I excited about the possibility that

something so easy, so healthy, so affordable (cost is all relative) just might

be making a huge difference in the future my child will have? Excited beyond

belief!

Lori

>

>

> Its very easy to read numbers but very difficult to visualise progress

because progress is an unmeasurable quantity.

>

> My son has double diagnosis. We have tried everything under the roof...ABA, 4x

speech[not PROMPT], OT, TOmatis Litsening Therapy, Hippotherapy, Biomedical,

neurofeedback, chiropractic treatment, accupuncture, NACD.... He still has not

shown any surges...even though he has made progress. When Nutriiveda was first

mentioned I jumped right away because it was something within my territory. I

have known 90% of the ingredients from my childhood.

> We cannot afford lots of stuff and it is expensive for us....our household

runs from paycheck to pay check...but we are ready to do anyting to help our

son. Especially when something is ALL NATURAL we are all for it.

> There are still no concrete study to say why our kids are like this why they

struggle to communicate, why they are " different " from the rest. No matter what

the reasons are - it has not stopped anyone among us from looking for

answers....looking for that RAY OF LIGHT , THAT HOPE - that things will turn

arround and that you would hear that little sweet voice calling out to you. The

day I hear my son talk in sentences is sure going to be PRICELESS.

> sowmya

>

>

>

>

>

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