how fast does NV work?

[Guest guest]

Hi everyone,

I started my 4 yr old daughter Evangeligue on NV 2 weeks ago today. She is

getting 2 scoops per day mixed with water put through her feeding tube. So far I

have not seen any surges or changes. I am keeping a daily diary and am very

eager to see some results. I have a few questions:

1. On average how long did it take you notice any differences in your kids?

2. Have there been any kids where NV just did not work for them?

thanks all

Sam

On 2010-09-26, at 9:25 PM, kiddietalk wrote:

> I've run this group for over a decade now and the success rate no matter how

severe the child is when first diagnosed is extremely high for those parents in

this group. It doesn't appear that those stats yet reflect to those children who

have parents that don't know how to advocate and secure appropriate services and

placement. In addition in this group we have for the past decade recommended in

addition to traditional speech and occupational therapy to explore multisensory

and alternative therap ies. Have you read The Late Talker book?

>

> Also over the years most in this group use fish oils (the essential fatty

acids) and more recently we are having even more dramatic and quicker surges

with NV (essential amino acids and essential nutrients from whole foods)

>

> My apraxic son Tanner was diagnosed severe profound apraxic at 2 years 10

months. He also was diagnosed with oral apraxia, dysarthria, sensory integration

dysfunction, hypotonia and motor planning deficits as well throughout his body.

He required speech, occupational and physical therapy. No matter how much

therapy he had his progress was painfully slow until I discovered fish oils

which helped him tremendously throughout most of his life. My son Tanner has

been mainstreamed since kindergarten and is a good kid. Outside of a product

called Pharma Omega Speak which has mega vitamin e in it that created MASSIVE

regressions in my poor son which lasted for months- the rest has been awesome

-but it wasn't until NV that Tanner went from having any apraxia quirks to well

above normal in various areas (see http://pursuitofresearch.org/pursuit.html as

much of what is there first started with Tanner but many others today are seeing

the same)

>

> So to answer your question...from what I have seen more so than the severity

of the initial diagnosis, prognosis for verbal disabled children depends greatly

on the involvement of the parents -and being your are here...your child is one

of the lucky ones!

>

> There honestly is so much hope!! And please please if you have not yet -read

The Late Talker for basic advocacy and other info to learn how to secure

appropriate therapy -and please look into fish oils and NV!!!

>

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