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Donna, I can't wait to read your reviews on the new Turbo Jams! You are always so thorough and so "right on". I won't be getting mine for awhile, so I'm eager to hear what you have to say!

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Donna, I can't wait to read your reviews on the new Turbo Jams! You are always so thorough and so "right on". I won't be getting mine for awhile, so I'm eager to hear what you have to say!

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Hi ,

I will try to do a review tomorrow - the plan is CPM

#3 for tomorrow. Thanks for the compliments on my

reviews :> Wish I could get paid for doing them! LOL!

Donna

--- Pink Pussycat

<pinkpussycat@...> wrote:

> Donna, I can't wait to read your reviews on the new

> Turbo Jams! You are always so thorough and so

> " right on " . I won't be getting mine for awhile, so

> I'm eager to hear what you have to say!

>

>

>

__________________________________________________

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Guest guest

Hi ,

I will try to do a review tomorrow - the plan is CPM

#3 for tomorrow. Thanks for the compliments on my

reviews :> Wish I could get paid for doing them! LOL!

Donna

--- Pink Pussycat

<pinkpussycat@...> wrote:

> Donna, I can't wait to read your reviews on the new

> Turbo Jams! You are always so thorough and so

> " right on " . I won't be getting mine for awhile, so

> I'm eager to hear what you have to say!

>

>

>

__________________________________________________

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  • 4 years later...
Guest guest

My 19 year old AS son just got his California Driver's License!!!

The best thing I ever did was take him out of school, away from " The Experts and

Professionals " and the horrible middle schoolers. Took him off all meds and

just let him be for a year. I would take him everywhere with me. Made him talk

to clerks and pay for things himself. I told him that in College I was a sign

language interpreter and now I was here to be his interpreter. Then we started

an intensive Homeschool DVD program.

He started growing up and going to a Youth group at church. He just finished

his 2nd semester at Community College and has friends and an active social life.

I NEVER thought this would happen. During the dark days I wanted to die. He

has always been the kindest, sweet, gentle person and I think that's what was

the saddest thing. He is gorgeous and the girls love him!! He said to me,

" It's a good thing I'm a good guy or I could really have a lot of girlfriends at

one time. " But like Pavlov's dog I still react if something seems wrong. The

10 mins waiting for him to do his driving test was like reliving all the phone

calls and problems at once. I told the examiner, " The next 10 mins could change

my life. "

I am so proud of him and just wanted to share some good news!!!

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  • 3 months later...

That's incredible! I'm so happy to hear those kinds of numbers!aFrom: NIck Guthe <nickguthe@...>infantile scoliosis treatment Cc: Montoya <isop06@...>Sent: Mon, August 30, 2010 5:42:00 PMSubject:

GOOD NEWS!!!

Thank you to all of the parents who let us put their adorable kids in casts in the PSA, we found out from that www.infantilescoliosis.org was averaging around 2,000 visits a month before the PSA aired on TV this year, and afterwards, it has added up to about 750,000 visits to ISOP this year so far! We are SO thrilled that the word is getting spread to more parents out there, and with 's work to get more distribution of the PSA this fall on more channels, it should reach more and more kids who need this treatment. Wow.There certainly would be no PSA or Metha/EDF casting in the U.S. without 's tireless, FIERCE work and beautiful Liv's difficult journey. And there would be no PSA without

Dr. Mehta and Shriners Hospitals and all of the doctors doing this work!!! Heroes, every one. is our champion! So nice to hear GOOD NEWS!!! : ) Heidi, Bexon's Mommy, (3 years old, in 8th cast from Salt Lake City Shriners, currently down from 62 degrees to 20 in cast)

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Wow, this is incredible! I so agree! And it all comes down to children who

have been helped -- whose lives have been so positively touched when they needed

it most. Incredible!

Shauna

Mother of Kieran (2nd cast), Kelsey and

>

> Thank you to all of the parents who let us put their adorable kids in casts in

> the PSA, we found out from that www.infantilescoliosis.org was

averaging

> around 2,000 visits a month before the PSA aired on TV this year, and

> afterwards, it has added up to about 750,000 visits to ISOP this year so far!

>

>

> We are SO thrilled that the word is getting spread to more parents out there,

> and with 's work to get more distribution of the PSA this fall on more

> channels, it should reach more and more kids who need this treatment. Wow.

>

> There certainly would be no PSA or Metha/EDF casting in the U.S. without

> 's tireless, FIERCE work and beautiful Liv's difficult journey. And

there

> would be no PSA without Dr. Mehta and Shriners Hospitals and all of the

doctors

> doing this work!!! Heroes, every one.

>

> is our champion! So nice to hear GOOD NEWS!!! : )

>

> Heidi, Bexon's Mommy, (3 years old, in 8th cast from Salt Lake City Shriners,

> currently down from 62 degrees to 20 in cast)

>

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That is amazing news!! Patty, mom of Isabella, 3 years old, in 7th scoli cast (Rochester) & mom to (9) & Evan(6)From: NIck Guthe <nickguthe@...>infantile scoliosis treatment Cc: Montoya <isop06@...>Sent: Mon, August 30, 2010

5:42:00 PMSubject: GOOD NEWS!!!

Thank you to all of the parents who let us put their adorable kids in casts in the PSA, we found out from that www.infantilescoliosis.org was averaging around 2,000 visits a month before the PSA aired on TV this year, and afterwards, it has added up to about 750,000 visits to ISOP this year so far! We are SO thrilled that the word is getting spread to more parents out there, and with 's work to get more distribution of the PSA this fall on more channels, it should reach more and more kids who need this treatment. Wow.There certainly would be no PSA or Metha/EDF casting in the U.S. without 's tireless, FIERCE work and beautiful Liv's difficult journey. And there would be no PSA without

Dr. Mehta and Shriners Hospitals and all of the doctors doing this work!!! Heroes, every one. is our champion! So nice to hear GOOD NEWS!!! : ) Heidi, Bexon's Mommy, (3 years old, in 8th cast from Salt Lake City Shriners, currently down from 62 degrees to 20 in cast)

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That is amazing news!! Patty, mom of Isabella, 3 years old, in 7th scoli cast (Rochester) & mom to (9) & Evan(6)From: NIck Guthe <nickguthe@...>infantile scoliosis treatment Cc: Montoya <isop06@...>Sent: Mon, August 30, 2010

5:42:00 PMSubject: GOOD NEWS!!!

Thank you to all of the parents who let us put their adorable kids in casts in the PSA, we found out from that www.infantilescoliosis.org was averaging around 2,000 visits a month before the PSA aired on TV this year, and afterwards, it has added up to about 750,000 visits to ISOP this year so far! We are SO thrilled that the word is getting spread to more parents out there, and with 's work to get more distribution of the PSA this fall on more channels, it should reach more and more kids who need this treatment. Wow.There certainly would be no PSA or Metha/EDF casting in the U.S. without 's tireless, FIERCE work and beautiful Liv's difficult journey. And there would be no PSA without

Dr. Mehta and Shriners Hospitals and all of the doctors doing this work!!! Heroes, every one. is our champion! So nice to hear GOOD NEWS!!! : ) Heidi, Bexon's Mommy, (3 years old, in 8th cast from Salt Lake City Shriners, currently down from 62 degrees to 20 in cast)

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