Updates for Dawn's 2 children prone to seizures on nutriiveda

[Guest guest]

Vinny and Lily 2 Months on NV update

Hi, things are going well. I don't know if I said this already but I did speak

to my kids neurologist and he was very intrigued and told me to keep giving it

to them because he noticed that something was different about them from their

prior visit( didn't tell him until end of appt.)Anyway, great progress for my

son in school regarding focus, participation and getting things correct. Also,

more words heard in school( he has always not said anything in school at all

before NV)This morning he was watching a repeat of the Knicks game and I was

turned away from him and I heard " shoot " so I said " shoot what Vin? " and he goes

" shoot the ball " WOW!! Then yesterday my daughter's teacher tells me that in

music theyn were singing the spongebob song and they put the microphone to her

for her turn and she said " spongebob " 3 times!! My daughter is even more

non-verbal than my son.Also at a party over the weekend, I was helping Lily eat

cake ( white dress ) and I guess I was talking too much, I felt her tap me on

the arm, so I said " what do you want Lil? " and I hear " I wan mo " > Thing s are

surprising me all the time, the teachers and therapists still don't know

anything about that they are taking NV, And I'm going to just keep going with

this! Good Luck All~~Dawn Falley Mom to Vinny(13, seizure disorder, PDD,

agenesis of the corpus collosum) & Lily(9, seizure disorder, PDD)

dawn falley (daffy4@...)

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Don't forget to print out survey so you know what to look for here

http://pursuitofresearch.org/NutriiVeda%20Survey.pdf

(and link for online survey here http://pursuitofresearch.org/survey.html )

Sample of some other testimonies here

http://pursuitofresearch.org/testimonials.html

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