hello

[Guest guest]

I found the most information about respite care and special summer schools for children with learning disabilites from the resource teacher at my sons school, he goes there for one on one throughout the day. The have given me such hope! kk61377 <kekerr@...> wrote: Roxanna, what a small world! I would like to know whether you havehad positive experiences in dealing with your child's school. If sowhat are they? What are the negative experiences. What do you feel youhelp you more.

Thanks, so much!>> What do you want to know. I am in Medina!> > Roxanna> Autism Happens> ( ) hello> > > Hello,> I am a student at Kent State University taking a class on> Parent/teacher collaboration. I am looking to talk to some people> about their experiences with a special ed. teacher and the IEP process> to learn what is helpful and what you feel could be done better. I am> really looking forward to talking with some of you and gaining some> valuable insight.>

Thanks!!!!>

Never miss an email again! Toolbar alerts you the instant new Mail arrives. Check it out.

[Guest guest]

My daughter is a Kent State graduate, class of 2005.

Suzanne

-- Re: ( ) hello

Roxanna, what a small world! I would like to know whether you havehad positive experiences in dealing with your child's school. If sowhat are they? What are the negative experiences. What do you feel youhelp you more. Thanks, so much!>> What do you want to know. I am in Medina!> > Roxanna> Autism Happens> ( ) hello> > > Hello,> I am a student at Kent State University taking a class on> Parent/teacher collaboration. I am looking to talk to some people> about their experiences with a special ed. teacher and the IEP process> to learn what is helpful and what you feel could be done better. I am> really looking forward to talking with some of you and gaining some> valuable insight.> Thanks!!!!>

[Guest guest]

Hi Angel

Where abouts do you live in Kansas? I live in northeast Kansas and have a

son who is 11 with autism. I also have an older boy who is 13.

************************************** See what's free at http://www.aol.com.

[Guest guest]

Ok We live in Topeka. Not too far away. Its nice to meet you.

************************************** See what's free at http://www.aol.com.

[Guest guest]

Hi,

You must be in my class. I am not having any luck on interviewing people. Can

you help?? All responses, I have received are very short. Can you please let me

know what you have done?? (time is running out)

Thanks rb

--

ph W. Bandiera

9632 Simsbury Court

Twinsburg, Ohio 44087

---- kk61377 <kekerr@...> wrote:

Hello,

I am a student at Kent State University taking a class on

Parent/teacher collaboration. I am looking to talk to some people

about their experiences with a special ed. teacher and the IEP process

to learn what is helpful and what you feel could be done better. I am

really looking forward to talking with some of you and gaining some

valuable insight.

Thanks!!!!

[Guest guest]

Hi ,

I live in the Olathe Gardner area. We go bowling in Olathe every

Friday. They have 99 cent games. He loves it. It is so nice to meet

you.

(Angel)

>

> Hi Angel

> Where abouts do you live in Kansas? I live in northeast Kansas

and have a

> son who is 11 with autism. I also have an older boy who is 13.

>

>

>

>

>

> ************************************** See what's free at

http://www.aol.com.

>

>

>

[Guest guest]

Welcome to the list. Sounds like a DDI hair elements test with counting rules

applied would provide some useful info for your mother and your son. How many

mercury amalgam dental fillings does she have? You can order them without a doc

through Direct Lab Services. If you mention this list, they'll give you a

discount.

S S

Hello everyone,

I have signed up to a few groups and don't remember the ones I

introduced myself on so I am just going to reintroduce myself. My

name is . I am a mother of the most wonderful boy I know. His

name is Shane, and he is autistic. We live in Kansas. It is so

upsetting that I can not seem to find any help in Kansas. We have

been been self employed for many years. The company that we sub

contracted for hired my husband to work hourly. It was a huge

blessing. My son has been the only one with health INS in our family,

but now the Gov is taking that away from my son cause they say $2000

is to much money for 3 people. Now of course they finally opening an

autism resource wing at one of the hospital here. First we had

insurance and no doc that worked with autism and now we have a whole

wing and no INS.

We loved the schools here. They did such a wonder for him. Then

in 7th grade they dropped the ball. So now I am now home schooling

him. He loves it. Before he would make him self sick cause he was so

stressed out about going to school. I can't find any help, or groups.

They schools wont even talk to me, the gov is now not helping and I

can't find the grants everyone says is so easy to get. We do go

bowling every Friday. My best friend goes with us. Now the summer

movie pack is starting but he really wants to play with other

children. He loves to draw and I found a teacher to come work with

him but no funds. I am so lost and at time can't breath. I am so

happy that June 11th is the first time autism has its day in court. I

am also surprised how many spell Autism -Autisum.

O we are trying to move to Branson Mo. It is the only place on

earth that my son loves. He takes after me it is the only place I

feel at home in my soul. WE are looking for land there so we can put

our trailer on and my parents can live next door to us. My son needs

them closer and so do I . My mom has Neuropathy, Polysystic Kidneys,

Lupus, Rheumapoid arthritis, and auto immune disease. My father has

had colon cancer twice. Sorry so long. Hope to meet some new friends

and get some information on some help. Have a wonderful day. God

bless you all.

_______________________________________________

Join Excite! - http://www.excite.com

The most personalized portal on the Web!

[Guest guest]

Hi - I don't think it will be too late, but getting the helmet as early as possible for optimizing growth is important. Can you call them and 'nag' a bit to get an earlier appt?? I did, and my daughter was helmeted at 5.75 mo rather than a bit over 6 mo.

HELLO

HI, IM NEW HERE, MY 6MO OLD DAUGHTER [VALERIA] WAS JUST DIAGNOSED WITH

TORTICOLLIS AND SEVERE PLAGIO. I NOTICED THIS SINCE SHE WAS ABOUT 2-3

WEEKS OLD AND MY PEDIATRICIAN TOLD ME NOT TO WORRY AND THAT IT WOULD

CORRECT ITSELF AND SHE WILL BE FINE, BUT HER CONDITION WORSENED AND BY

THE TIME I SAW A SPECIALIST IT WAS ALREADY SEVERE. SHE WAS JUST

DIAGNOSED AND HER APPOINTMENT WITH CRANIAL TECH. WILL BE UNTIL SHES

ALREADY 7 ALMOST 8MOS. I WAS WONDERING IF ITS NOT GOING TO BE TOO

LATE. ANY ADVICE?

-FRANCES

AOL now offers free email to everyone. Find out more about what's free from AOL at AOL.com.

[Guest guest]

Hello. unfortunately, your story is like a lot of other peoples. SO

many pediatricians say " don't worry about it " , or it will round out

on it's own, etc. But, sadly that just isn't often the case.

My Daughter got her band shortly after 7mo and she got great

correction. MANY babies get their bands after 7mo.... some even

after a year old and still get great correction. So, don't worry too

much.... you still have time to see some great growth and

correction.

Keep us updated.

Jen

katie (3 yrs), Hanger Band Grad

(5 1/2 yrs)

>

> HI, IM NEW HERE, MY 6MO OLD DAUGHTER [VALERIA] WAS JUST DIAGNOSED

WITH

> TORTICOLLIS AND SEVERE PLAGIO. I NOTICED THIS SINCE SHE WAS ABOUT

2-3

> WEEKS OLD AND MY PEDIATRICIAN TOLD ME NOT TO WORRY AND THAT IT

WOULD

> CORRECT ITSELF AND SHE WILL BE FINE, BUT HER CONDITION WORSENED AND

BY

> THE TIME I SAW A SPECIALIST IT WAS ALREADY SEVERE. SHE WAS JUST

> DIAGNOSED AND HER APPOINTMENT WITH CRANIAL TECH. WILL BE UNTIL SHES

> ALREADY 7 ALMOST 8MOS. I WAS WONDERING IF ITS NOT GOING TO BE TOO

> LATE. ANY ADVICE?

>

> -FRANCES

>

[Guest guest]

-

Hello!

My little one started wearing her helmet around 8 mos. of age. After

3 mos. her flat spot grew out 1/4 of an inch. This is just one of

many positive stories that you will read about from other moms. Each

childs rate of growth is very different. Some months I see results

and others not as much. I have read stories from this group that

will amaze you. Some babies started over 12 mos. of age and achieved

amazing results. It is going to be a lengthy process. My child has

had her helmet for 4 months now. It may take another 2 mos. or

perhaps longer I do not know. At this point the helmet seems part of

her. She has pretty severe plagio as well. However, each month I

see little changes that keep my spirits up.

I wish you and Valeria the best. Just keep reading these messages

and asking questions. I went from being filled with worrry to

feeling at ease and much more positive about my daughters situation

thanks to this goup of parents.

Kristi, mother to Ellie 9 mos. tort./plagio.

-- In Plagiocephaly , " Frances Delgadillo "

<xkaramosa_gphio@...> wrote:

>

> HI, IM NEW HERE, MY 6MO OLD DAUGHTER [VALERIA] WAS JUST DIAGNOSED

WITH

> TORTICOLLIS AND SEVERE PLAGIO. I NOTICED THIS SINCE SHE WAS ABOUT

2-3

> WEEKS OLD AND MY PEDIATRICIAN TOLD ME NOT TO WORRY AND THAT IT

WOULD

> CORRECT ITSELF AND SHE WILL BE FINE, BUT HER CONDITION WORSENED AND

BY

> THE TIME I SAW A SPECIALIST IT WAS ALREADY SEVERE. SHE WAS JUST

> DIAGNOSED AND HER APPOINTMENT WITH CRANIAL TECH. WILL BE UNTIL SHES

> ALREADY 7 ALMOST 8MOS. I WAS WONDERING IF ITS NOT GOING TO BE TOO

> LATE. ANY ADVICE?

>

> -FRANCES

>

[Guest guest]

Welcome !

This is a wonderful group of helpful parents. Feel fre to ask any questions you have - or look thru old messages to see what has been discussed in the past!

Jen and Luli - 22 months

Left tort - Right Plagio - Hanger Band Grad - CA

http://www.babiesonline.com/babies/j/jens5th/

hello

hi my name is kristen and i have a 5 month old son who has

plagiocephly. he hasnt been fitted for a helmet yet but will be or

should i say should be by the end of the month. i am a little scared

about this whole thing. i guess it is because i dont know what to

expect. i came acroos this group hoping to meet moms who are or did go

though what i am going though and to hopefully and to get answer on

what i should except will happen and if it is being done right. so

basically i write this message with the title please help me to

understand what i will be going through.

Email and AIM finally together. You've gotta check out free AOL Mail!

[Guest guest]

Hi !

I joined the group a week or so ago, and my son is 1 week into wearing his helmet 23 hrs. This group has been very informative, and I wish I would have found it before we got his helmet, so you are lucky! Good luck with everything!

Jodie

>> hi my name is kristen and i have a 5 month old son who has > plagiocephly. he hasnt been fitted for a helmet yet but will be or > should i say should be by the end of the month. i am a little scared > about this whole thing. i guess it is because i dont know what to > expect. i came acroos this group hoping to meet moms who are or did go > though what i am going though and to hopefully and to get answer on > what i should except will happen and if it is being done right. so > basically i write this message with the title please help me to > understand what i will be going through.>

[Guest guest]

Hi Leah,

When you consider the alternative to banding, which is not banding

and potentially allowing your child's head to remain deformed with

potential consequences, I think the 5 hour drive each way is well

worth it. We drove from Tulsa to Dallas every week and I'd do it

again in a heartbeat. I couldn't live with myself if I didn't do

anything to correct something that is so correctable, only to have

my daughter be teased or have medical complications later on down

the road. It's a personal choice and you have to go with your gut

on this, but for me personally, I felt that banding was the only

option. And I've never looked back and my daughter's head looks

incredible now!

Good luck with your decision,

Lori

Mom to , 9 months

DOC Band grad July 07

>

> I am a new member and am just reading all the messages. I

hate

> to be the sourpuss, but I am not near as positive as you all are!

My

> daughter is almost 6 months and was diagnosed with brachycephalic.

> We

> are going to the neurosurgeon on Thursday to see what he thinks.

My

> overwhelming feeling right now is GUILT! As a first time mom, I

did

> not know how important it was to rotate sleeping positions!!!! My

> doctor did notice the back of her head becoming flat at her 2 and

> 4-month check-up, but she did NOT make a big deal about it!!! She

> actually told me at her 4-month check-up that even if I tried

> switching her sleeping position, would probably just end up

on

> her back....so I felt there wasn't much bother in doing it. Well,

> after a trip home to my parents my mother INSISTED I see another

> doctor. She (my mother) is a Labor & Delivery nurse for 30+ years

> and

> had not seen a babies head shaped as 's was. So, I took her

in

> and now am having these terrible guilty feelings that this could

have

> been prevented!!!! Also, am I the only one that does not like the

> looks of the helmets???? In this age of technology, can't there

be

> anything that looks better to the eye? I don't want to sound so

> pessimistic, as I know there are sooooo many other things that my

> angel could have, but I feel this is MY fault!!!! Also, if anyone

> can

> tell me what is soooo bad about the helmets and soooo good about

the

> bands, I would appreciate it. Is it worth traveling 5+ hours for

the

> bands each way? If these bands are soooo good, why aren't they

> available in every city? Sorry to ramble.

>

> If you have the time to look, I have put 's pictures of her

> flat

> head on my website and would appreciate anyone looking at them to

> compare if their child had improvement with a similar looking

head.

> http://www.geocities.com/leah_black/brachy.html

>

> Thank you,

> Leah

>

[Guest guest]

please list the products.

[ ] Hello

Hello all,

I am a new member to this group and have found some products that

really help with many different issues. We found the products because

our son was having difficulty saying his " s and g " sounds. The

doctors recommended speech therapy. We found these amazing products.

We put him on the products and within 1 month he was pronouncing his

letters and sounds better. He was learning things much quicker and

catching onto things better as well. The daycare had been working

with him very closely and called me into the office one day for a

conference. They asked me what I had changed in the last month with

regards to his learning. I told them nothing, we were still doing the

same things that we had done before I found these products. They

asked what products they were and I told them. They had never heard

of them, but said that whatever they are, they are working, keep

doing it.

If anyone is interested in these great products, please feel free

to contact me at any time. I would love to help anyone and answer

questions you may have.

Thanks,

Sarita Blanchette

[Guest guest]

I completely agree with Lori. We chose to band for the same

reasons...I didn't want my son teased or to have medical

complications later on. Even if you rotated your daughter's head,

it might not have helped. We repositioned our son for 4 months and

didn't see improvement. I do think it kept his head from getting

worse but we definitely didn't have any improvement. We went to CT

at 3 months and finally banded at 7.5 months...both measurements

were the exact same. I would think the 5 hour drive would be worth

it. We were very pleased with our results. My guess is that the

band/helmet is not readily available because the whole abnormal

headshapes is a more recent problem due to the back to sleep

program. Good luck in your decision.

PS: The babies look so cute in their helmets and you can make them

cute...we used stickers and changed them every week to every other

week.

I think people interchange helmets and bands. If there is a

difference, my guess is that a helmet covers more of the head but I

really don't know.

> >

> > I am a new member and am just reading all the messages. I

> hate

> > to be the sourpuss, but I am not near as positive as you all

are!

> My

> > daughter is almost 6 months and was diagnosed with

brachycephalic.

> > We

> > are going to the neurosurgeon on Thursday to see what he

thinks.

> My

> > overwhelming feeling right now is GUILT! As a first time mom, I

> did

> > not know how important it was to rotate sleeping positions!!!!

My

> > doctor did notice the back of her head becoming flat at her 2

and

> > 4-month check-up, but she did NOT make a big deal about it!!!

She

> > actually told me at her 4-month check-up that even if I tried

> > switching her sleeping position, would probably just end

up

> on

> > her back....so I felt there wasn't much bother in doing it.

Well,

> > after a trip home to my parents my mother INSISTED I see another

> > doctor. She (my mother) is a Labor & Delivery nurse for 30+

years

> > and

> > had not seen a babies head shaped as 's was. So, I took

her

> in

> > and now am having these terrible guilty feelings that this could

> have

> > been prevented!!!! Also, am I the only one that does not like

the

> > looks of the helmets???? In this age of technology, can't there

> be

> > anything that looks better to the eye? I don't want to sound so

> > pessimistic, as I know there are sooooo many other things that

my

> > angel could have, but I feel this is MY fault!!!! Also, if

anyone

> > can

> > tell me what is soooo bad about the helmets and soooo good about

> the

> > bands, I would appreciate it. Is it worth traveling 5+ hours

for

> the

> > bands each way? If these bands are soooo good, why aren't they

> > available in every city? Sorry to ramble.

> >

> > If you have the time to look, I have put 's pictures of her

> > flat

> > head on my website and would appreciate anyone looking at them

to

> > compare if their child had improvement with a similar looking

> head.

> > http://www.geocities.com/leah_black/brachy.html

> >

> > Thank you,

> > Leah

> >

>

[Guest guest]

The company is called Nikken. There is a website you

can go to at

www.nikken.com/chrisblanchette

This website will give you lots of different

information. I will send you a couple of testimonials

which happen to be of autistic children, but he has

had many of the same results.

We are using the water system, the air system, and

the insoles with him. There are also nutritionals and

other supplements that you can use. We haven't gotten

to those yet, because we have been truly amazed with

the progress he has shown so far.

Sarita

--- Colleen Somerville

<colleen.somerville@...> wrote:

> please list the products.

>

> [ ] Hello

>

>

>

> Hello all,

>

> I am a new member to this group and have found some

> products that

> really help with many different issues. We found the

> products because

> our son was having difficulty saying his " s and g "

> sounds. The

> doctors recommended speech therapy. We found these

> amazing products.

> We put him on the products and within 1 month he was

> pronouncing his

> letters and sounds better. He was learning things

> much quicker and

> catching onto things better as well. The daycare had

> been working

> with him very closely and called me into the office

> one day for a

> conference. They asked me what I had changed in the

> last month with

> regards to his learning. I told them nothing, we

> were still doing the

> same things that we had done before I found these

> products. They

> asked what products they were and I told them. They

> had never heard

> of them, but said that whatever they are, they are

> working, keep

> doing it.

>

> If anyone is interested in these great products,

> please feel free

> to contact me at any time. I would love to help

> anyone and answer

> questions you may have.

>

> Thanks,

> Sarita Blanchette

>

>

>

>

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

________________________________________________________________________________\

____

Catch up on fall's hot new shows on TV. Watch previews, get listings, and

more!

http://tv./collections/3658

[Guest guest]

Hi Sarita,

Please let us know the products.

[childrensapraxiane t] Hello

Hello all,

I am a new member to this group and have found some products that

really help with many different issues. We found the products because

our son was having difficulty saying his " s and g " sounds. The

doctors recommended speech therapy. We found these amazing products.

We put him on the products and within 1 month he was pronouncing his

letters and sounds better. He was learning things much quicker and

catching onto things better as well. The daycare had been working

with him very closely and called me into the office one day for a

conference. They asked me what I had changed in the last month with

regards to his learning. I told them nothing, we were still doing the

same things that we had done before I found these products. They

asked what products they were and I told them. They had never heard

of them, but said that whatever they are, they are working, keep

doing it.

If anyone is interested in these great products, please feel free

to contact me at any time. I would love to help anyone and answer

questions you may have.

Thanks,

Sarita Blanchette

[Guest guest]

Hi,

I know for me I was so worried about the band but it really was no big

deal. Our son adjusted right away. We went at 3 months due to

noticing a preference in looking to his left. At 3 months, CT told us

he'd benefit from a band but we chose to ask our ped. Our ped. said

to wait till 6 months then he kind of waffled on whether we should

wait till 9 months or not. His final thing was wait but we decided to

go back to CT at 6.5 months. Our son got his band at 7.5 months. We

were really pleased with the results. He graduated at 9.5 months and

is now 15 months. I can still notice a little bit of the flattening

but no one else would. The process...(at least at CT)...you go for a

scan or cast (different locations are different), then you go back 10-

14 days later to get fitted for the band. CT will give you

instructions to prevent skin breakdown. We never had a skin issue and

we live in PHX, AZ so it is hot. Then you go back the following week

for an adjustment. Due to your son's age, I think you'll have to go

weekly at first opposed to bi-weekly since the younger they are the

faster they grow. During each visit, they will make adjustments to

the band based on growth to allow for new growth. Some babies have a

harder time sleeping at night. Our son did the first 2 nights but we

just kept playing with his PJ's and the temp of our house. By night

3, he was back to sleeping 11-12 hours straight. Hope this helps.

Good luck.

>

> hi my name is kristen and i have a 5 month old son who has

> plagiocephly. he hasnt been fitted for a helmet yet but will be or

> should i say should be by the end of the month. i am a little scared

> about this whole thing. i guess it is because i dont know what to

> expect. i came acroos this group hoping to meet moms who are or did

go

> though what i am going though and to hopefully and to get answer on

> what i should except will happen and if it is being done right. so

> basically i write this message with the title please help me to

> understand what i will be going through.

>

[Guest guest]

Please let us know the product. Very interested.

Kathy

[ ] Hello

Hello all,

I am a new member to this group and have found some products that

really help with many different issues. We found the products because

our son was having difficulty saying his " s and g " sounds. The

doctors recommended speech therapy. We found these amazing products.

We put him on the products and within 1 month he was pronouncing his

letters and sounds better. He was learning things much quicker and

catching onto things better as well. The daycare had been working

with him very closely and called me into the office one day for a

conference. They asked me what I had changed in the last month with

regards to his learning. I told them nothing, we were still doing the

same things that we had done before I found these products. They

asked what products they were and I told them. They had never heard

of them, but said that whatever they are, they are working, keep

doing it.

If anyone is interested in these great products, please feel free

to contact me at any time. I would love to help anyone and answer

questions you may have.

Thanks,

Sarita Blanchette

________________________________________________________________________________\

____

Pinpoint customers who are looking for what you sell.

http://searchmarketing./

[Guest guest]

I am very sorry, I forgot to send the attachments.

Here they are.

Sarita

--- Colleen Somerville

<colleen.somerville@...> wrote:

> please list the products.

>

> [ ] Hello

>

>

>

> Hello all,

>

> I am a new member to this group and have found some

> products that

> really help with many different issues. We found the

> products because

> our son was having difficulty saying his " s and g "

> sounds. The

> doctors recommended speech therapy. We found these

> amazing products.

> We put him on the products and within 1 month he was

> pronouncing his

> letters and sounds better. He was learning things

> much quicker and

> catching onto things better as well. The daycare had

> been working

> with him very closely and called me into the office

> one day for a

> conference. They asked me what I had changed in the

> last month with

> regards to his learning. I told them nothing, we

> were still doing the

> same things that we had done before I found these

> products. They

> asked what products they were and I told them. They

> had never heard

> of them, but said that whatever they are, they are

> working, keep

> doing it.

>

> If anyone is interested in these great products,

> please feel free

> to contact me at any time. I would love to help

> anyone and answer

> questions you may have.

>

> Thanks,

> Sarita Blanchette

>

>

>

>

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

________________________________________________________________________________\

____

Tonight's top picks. What will you watch tonight? Preview the hottest shows on

TV.

http://tv./

[Guest guest]

-

My son wore a helmet for severe Brachycephaly for 5 months (7-

12months). It was a very hard decision for us to make, but we decided

not to gamble with letting nature take its course.

It was a very long 5 months for us (mom and dad), but our son adopted

to the helmet in minutes and never looked back.

We would go every few weeks and study the measurements and each week

we would see progress. At the end of 5 months, our son's head looked

really great...not perfect, but much better.

My son is now 15 months old and his head is getting better and better,

as he is growing and his head shape is changing as he grows.

We are very happy we made the decision to first accept that our son's

head needed help and that we went ahead with helmet therapy. It is not

an easy decision, but take it from a parent with experience...it is

well worth it...and honestly, such a short period in their lives with

such lasting effects.

In terms of what to expect...not too much actually. You will either

have your child scanned or casted for the helmet. The helmet will

arrive and you will have your child wear it on/off for several hours a

day until they become used to it. Then, they basically wear it for 23

hours a day. You will need to clean the helmet everyday. And every few

weeks, you will go for a head measurement to see the progress. Once

they feel you have reached the ideal shape, you will be done and you

will graduate from the program. Your child will nap, sleep and play in

the helmet and adapt like they wore it since birth. Honestly, the

helmet does all the work. Just trust your doctors and everything will

fine.

>

> hi my name is kristen and i have a 5 month old son who has

> plagiocephly. he hasnt been fitted for a helmet yet but will be or

> should i say should be by the end of the month. i am a little scared

> about this whole thing. i guess it is because i dont know what to

> expect. i came acroos this group hoping to meet moms who are or did

go

> though what i am going though and to hopefully and to get answer on

> what i should except will happen and if it is being done right. so

> basically i write this message with the title please help me to

> understand what i will be going through.

>

[Guest guest]

The products are from a company called Nikken. They

use magnetics and far-infrared technologies. They also

have whole foods, vitamins, and they have a new

products that helps rebuild your bones. All of the

whole foods and supplements are all natural so you

don't need to worry about the side effects. The

products have many years of research before released

to the public. The website is

www.nikken.com/chrisblanchette

If you have any other questions or would like to

discuss further, please feel free to email me or give

me a call at 360-624-6372.

Sarita

--- Kathy Ruiz <laloquita31@...> wrote:

> Please let us know the product. Very interested.

>

> Kathy

>

>

> [ ] Hello

>

> Hello all,

>

> I am a new member to this group and have found some

> products that

> really help with many different issues. We found the

> products because

> our son was having difficulty saying his " s and g "

> sounds. The

> doctors recommended speech therapy. We found these

> amazing products.

> We put him on the products and within 1 month he was

> pronouncing his

> letters and sounds better. He was learning things

> much quicker and

> catching onto things better as well. The daycare had

> been working

> with him very closely and called me into the office

> one day for a

> conference. They asked me what I had changed in the

> last month with

> regards to his learning. I told them nothing, we

> were still doing the

> same things that we had done before I found these

> products. They

> asked what products they were and I told them. They

> had never heard

> of them, but said that whatever they are, they are

> working, keep

> doing it.

>

> If anyone is interested in these great products,

> please feel free

> to contact me at any time. I would love to help

> anyone and answer

> questions you may have.

>

> Thanks,

> Sarita Blanchette

>

>

>

>

>

>

>

________________________________________________________________________________\

____

> Pinpoint customers who are looking for what you

> sell.

> http://searchmarketing./

>

> [Non-text portions of this message have been

> removed]

>

>

________________________________________________________________________________\

____

Be a better Heartthrob. Get better relationship answers from someone who knows.

Answers - Check it out.

http://answers./dir/?link=list & sid=396545433

[Guest guest]

>

> > please list the products.

> >

> > [ ] Hello

> >

> >

> >

> > Hello all,

> >

> > I am a new member to this group and have found some

> > products that

> > really help with many different issues. We found the

> > products because

> > our son was having difficulty saying his " s and g "

> > sounds. The

> > doctors recommended speech therapy. We found these

> > amazing products.

> > We put him on the products and within 1 month he was

> > pronouncing his

> > letters and sounds better. He was learning things

> > much quicker and

> > catching onto things better as well. The daycare had

> > been working

> > with him very closely and called me into the office

> > one day for a

> > conference. They asked me what I had changed in the

> > last month with

> > regards to his learning. I told them nothing, we

> > were still doing the

> > same things that we had done before I found these

> > products. They

> > asked what products they were and I told them. They

> > had never heard

> > of them, but said that whatever they are, they are

> > working, keep

> > doing it.

> >

> > If anyone is interested in these great products,

> > please feel free

> > to contact me at any time. I would love to help

> > anyone and answer

> > questions you may have.

> >

> > Thanks,

> > Sarita Blanchette

> >

> >

MIA's story

When Mia was born in 1997, she had a ventricular

septal defect, which is a

hole in her heart. By age 3 she still could not talk.

However, since we

lived in a multilingual town, most children her age

were slow to speak. As

a result, we were not particularly concerned.

But by the time she was about to attend kindergarten,

she still did not

speak, except whisper to us, her parents, and she was

extremely shy even

with us. When she would sleep, she would flip-flop

around in the bed like a

fish and therefore would not get any meaningful rest.

She also would grind

her teeth horribly while sleeping.

Though she constantly ate, she was always underweight

and suffered from

severe stomach pains. Mia was always terrified of

animals and would refuse

to go outside when she saw any animal. She was also

terrified of getting

dirty so she would run to the shower if she thought

she had a spot of dirt

on her.

When Mia started kindergarten, she still would not

speak to anyone, even the

teacher. Every day Mia would return home from school

with such anxiety that

she would literally kick holes in her bedroom wall,

physically attack her

sisters and brothers, and lay in a fetal position and

just scream for hours.

She eventually started seeing a series of

psychiatrists. Mia was diagnosed

with various forms of autism: selective mutism,

ashbergers, & ADHD. She went

through many drugs including Paxil, Prozac, Zoloft,

Ritalin, and then others

to counteract the side effects of these drugs. In

addition to all of this,

she was also diagnosed with enamel displasia, which

means that there is no

enamel on the teeth. So now, not only did she grind

her teeth in her sleep

but she also had no enamel to protect them. Throughout

kindergarten Mia

could not speak, read, or write, or do basic math. By

the end of

kindergarten, an iridologist put Mia on a vitamin

program. Her anxiety

eased up and she began to whisper to other kids.

In first grade, the medical doctors were still not

making any progress with

her. Academically she was making no progress either.

Towards the end of

the school year, I attended a Nikken wellness

presentation because I was

interested in the water and was talked into taking

home a sleep system. I

was not interested in the sleep system so I put it on

Mia's bed.

Immediately that night she slept like a log, did not

flip-flop around, and

did not grind her teeth for the first time ever in her

life. The next day

Mia's teacher called me crying and informed me that

Mia just stood up in

front of the class and read a book out loud! I

immediately bought Mia an

entire sleep system and noticed a complete

transformation in my daughter!

Mia could now speak, read, write, do math, and

maintain average grades in

school. She stopped being aggressive towards her

siblings, stopped having

anxiety attacks, stopped having severe stomach pain,

and she now loves to

play in the dirt and loves to play with any kind of

animal. This literally

happened overnight!

In the first few weeks following this transformation,

if she ever spent the

night off the sleep system, most of her symptoms would

immediately return.

After several months, we could go out of town for a

couple of days without

the sleep system and only then, would her symptoms

return. Now she can go

weeks without her sleep system (while traveling such

as our frequent

hurricane evacuations or camping trips) before showing

mild symptoms. For

example, she will become what is perceived by others

to be extreme shyness,

she have difficulty reading and writing, she will have

anxiety, and not get

along with her siblings.

Mia also drinks nothing but Optimized water. She

recognizes how good it

makes her feel and will turn down other forms of

water. She also drinks

Kenzen shakes, she takes Lactoferin Gold, and takes

shots of the Jade

enzymes. On a side note, her siblings absolutely crave

the Jade enzymes.

Prior to being discontinued, the Restful Night

capsules made a huge

difference in calming her at bedtime.

I believe that the Nikken magnets balanced Mia's

energy profoundly and

immediately. The nutritionals, water, and sleep system

have made her into a

completely normal and healthy person.

All of this without the use of drugs! Even her doctors

are amazed.

Sturt

Phone at home: 850-936-5806

Here is the other testimonial.

's Story

is my 4 year old daughter, A pretty girl

born with a lot of

difficulties. She was born with respiratory problems,

She had trouble

walking, trouble eating and chronic digestive problems

(*autistic

symptoms).

Non Verbal...not even sounds, Didn't smile or

Didn't laugh

(*depressed, I guess) Sleeping problems (no sleep)

Banged her head

against wall or furniture. No eye contact.

Sleep was hard to come by for my wife, We were

both really sad

ourselves because of our daughter's conditions. No

energy, No hope. No

solutions were offered, just bad news from doctors

saying it would only

get worse as she grew up. We were at wits end!

We were HOPING and PRAYING to get help...

Then one day I

bumped into Nikken and My life changed instantly

forever. When I got

home with the products my daughter was asleep and I

placed the magnetic

pad on the bed and placed on it.

WOW slept way better (breathing

was quiet) It was

a miracle. How could this be and Why didn't I know

about this

sooner....I was excited and upset at the same time.

I felt blessed but

could not understand why I had to wait 4 years to find

these great

products. spoke 5 days later (*we both were

hysterical). She

is now super happy, runs, jumps, talks, hugs, sings,

and daddy does too.

We are in love with life again. I see a better

future for my daughter

and my family. Thanks to these wonderful products. I

am forever

grateful

I wanted to share this with YOU & with everybody and

anybody.

Signed,

Al, A now very happy and excited man

Following is a link to a telephone interview with Dave

and

Weiss

http://wendyweiss.com/offers/followup-networkNikken.html

> >

> >

> >

> >

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

>

>

>

______________________________________________________________________

______________

> Tonight's top picks. What will you watch tonight? Preview the

hottest shows on TV.

> http://tv./

>

>

>

[Guest guest]

Right now we are using the PiMag water system, the Air

Power5, and the Kidstrides insoles. We are beginning

the whole foods and supplements this month along with

the sleep system.

Sarita

--- Kathy Ruiz <laloquita31@...> wrote:

> Hi Sarita,

> Please let us know the products.

>

>

> [childrensapraxiane t] Hello

>

> Hello all,

>

> I am a new member to this group and have found some

> products that

> really help with many different issues. We found the

> products because

> our son was having difficulty saying his " s and g "

> sounds. The

> doctors recommended speech therapy. We found these

> amazing products.

> We put him on the products and within 1 month he was

> pronouncing his

> letters and sounds better. He was learning things

> much quicker and

> catching onto things better as well. The daycare had

> been working

> with him very closely and called me into the office

> one day for a

> conference. They asked me what I had changed in the

> last month with

> regards to his learning. I told them nothing, we

> were still doing the

> same things that we had done before I found these

> products. They

> asked what products they were and I told them. They

> had never heard

> of them, but said that whatever they are, they are

> working, keep

> doing it.

>

> If anyone is interested in these great products,

> please feel free

> to contact me at any time. I would love to help

> anyone and answer

> questions you may have.

>

> Thanks,

> Sarita Blanchette

>

> [Non-text portions of this message have been

> removed]

>

>

>

>

>

>

>

________________________________________________________________________________\

____

> Got a little couch potato?

> Check out fun summer activities for kids.

>

http://search./search?fr=oni_on_mail & p=summer+activities+for+kids & cs=bz

>

>

> [Non-text portions of this message have been

> removed]

>

>

________________________________________________________________________________\

____

Don't let your dream ride pass you by. Make it a reality with Autos.

http://autos./index.html

[Guest guest]

Sarita,

Are you a Nikken consultant?

>

> > Hi Sarita,

> > Please let us know the products.

> >

> >

> > [childrensapraxiane t] Hello

> >

> > Hello all,

> >

> > I am a new member to this group and have found some

> > products that

> > really help with many different issues. We found the

> > products because

> > our son was having difficulty saying his " s and g "

> > sounds. The

> > doctors recommended speech therapy. We found these

> > amazing products.

> > We put him on the products and within 1 month he was

> > pronouncing his

> > letters and sounds better. He was learning things

> > much quicker and

> > catching onto things better as well. The daycare had

> > been working

> > with him very closely and called me into the office

> > one day for a

> > conference. They asked me what I had changed in the

> > last month with

> > regards to his learning. I told them nothing, we

> > were still doing the

> > same things that we had done before I found these

> > products. They

> > asked what products they were and I told them. They

> > had never heard

> > of them, but said that whatever they are, they are

> > working, keep

> > doing it.

> >

> > If anyone is interested in these great products,

> > please feel free

> > to contact me at any time. I would love to help

> > anyone and answer

> > questions you may have.

> >

> > Thanks,

> > Sarita Blanchette

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

> >

> >

> >

> >

> >

>

_____________________________________________________________________

_______________

> > Got a little couch potato?

> > Check out fun summer activities for kids.

> >

> http://search./search?

fr=oni_on_mail & p=summer+activities+for+kids & cs=bz

> >

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

>

>

>

_____________________________________________________________________

_______________

> Don't let your dream ride pass you by. Make it a reality with

Autos.

> http://autos./index.html

>