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Agreed.SPEAK is Not good for most (if not all) kids.

Warmest wishes,

Barbara

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

CEO/ Help Me Speak, LLC

<http://www.helpmespeak.com/> http://www.helpmespeak.com

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

2500 Wallington Way; Suite 103

Marriottsville, MD 21104

From:

[mailto: ] On Behalf Of Alberta

Sent: Friday, March 11, 2011 4:45 AM

Subject: Re: [ ] nutritionist

I know a mom who uses Speak and swears by it but I hate it. When I looked

up what it was, I was thinking, " Is she nuts??? " I don't like Speak for a

lot of reasons but the #1 reason why is because it has soy. The high levels

of Vit E in Speak is all soy. All soy in North America is GMO. Soy has

been linked so far to breast cancer and soy also has enzyme inhibitors, so

if your child has any pre-existing digestive issues, soy will exacerbate

it. If your child has any issues with milk, the molecular structure of the

soy protein is so similar to milk that the body cannot tell the difference

and the effect of soy will mimick the milk protein.

One might think that Vit E is a good thing but at those levels...personally,

I feel it's playing with fire. Vit E toxicity for a child who may or may

not have Vit E associated metabolic issues (and therefore elevated levels of

Vit E before starting any supplement) can have dire consequences. If you

look up what Vit E toxicity does to adults, you'll find that one of the

things it does cause is a hemorrahagic stroke. What will it do to kids with

pre-existing elevated levels of E due to metabolic issues? They would reach

toxicity levels much sooner than even a child with no metabolic issues.

I'm not saying whether or not Speak is bad for *everyone* because all our

kids have different issues and we do what we need to do as parents

but...putting aside the fact that it contains soy (I personaly really hate

soy), even if it were synthetic Vit E or ones (rarely) derived from other

sources like sunflower, suitable candidates for Speak would be kids who have

very major Vit E deficiencies. If you're unsure whether or not your child

has severe Vit E deficiencies, I wouldn't do it. And even if your child has

severe Vit E deficiencies, I would choose an alternate Vit E source other

than soy. Sometimes the inability to verbalize is not even associated with

Vit E and I would raise Vit E levels very cautiously when supplementing Vit

E separately, too. There is a relationship between Vit E, Zinc, and

Carnosine. That's already two other variables that Speak will not address

because Speak works under the assumption that there are no carnosine or zinc

deficiencies (which is a very broad assumption to make). Or it could be a

methylation issue, in which case you're totally barking up the wrong tree

and Speak will not resolve it. Then we could talk about viruses,

parasites...so many variables -- and Speak will DEFINITELY not address any

of these. It's a product with a very narrow scope.

I won't even get into the issue of possible pre-existing metabolic issues

with Vit K -- another source of possible complications that can arise from

using Speak. I don't know what people were thinking when they designed this

supplement. Insanely high sources of Vit K and Vit E. Stupid.

>

> 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

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

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

Speak_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-sh

ift-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-sh

ift-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-be

cause-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-dr

ugs-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,

>

>

>

>

> =====

>

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