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Hi Rochelle,

I think you're mum and Breann's Grandma would get along great. Once

things slow down for the family, I think that introducing them would be

fabulous! I am around all week, so whenever its convenient for you. When

are the kiddos on Spring Break?

We should get together then. Liv's break starts next week.

Cant wait to Devynn's films!!

Talk soon,

HRH

>

> Very well put. Tell Breanns Grandma we are deffinetly thinking

> of them. Also if she would like my mom would really like to meet

> them. She would love to offer them some support since they live so

> close. Also when do you need those x-rays and I will bring Devyn's

> down to you later this week.

> Rochelle

>

>

>>

>> I am sure that many of you have read Breanns Story on

>> www.infantilescoliosis.org Breann and Olivia have followed

> eachother on

>> this scoliosis journey, since they were 2 & 3 years old (they are

> now 10 &

>> 11). The Veptr didnt work out for Breann like everyone had hoped,

> and

>> last week it was decided that the best plan of action would be to

> remove

>> it. Last December 07, her left Veptr rod (dual hybrid attached to

> her

>> pelvic structure) was removed, and she was placed in a brace. Last

> week,

>> the right Veptr rod was removed, an anterior release was performed,

> 5

>> disks were removed, a rib was removed, and she was placed into a

> halo.

>> All of this, to prepare for her definitive spinal fusion in 3 to 6

> weeks.

>> As you can imagine, she is having a difficult recovery and enduring

> a lot

>> of pain. I am sharing this story in hopes that it will help

> someone new

>> on this forum to understand the importance of Early Treatment for

>> progressive infantile scoliosis. Infants diagnosed with the

> progressive

>> form of scoliosis do not have time to wait and watch. ET has the

> ability

>> to rid them of the deformity, gently & permanently, if applied

> properly.

>> ET can prevent them from living a life full of surgeries, a

> deformity ,

>> pulmonary issues & pain. There is a window of time that

> infants/children

>> can benefit from the Early Treatment Method, so learn as much as

> you can

>> about this method, and scoliosis, and take action now. The ISOP

> website

>> was dedicated to Breanns mum Joyce back in 02, and I know that she

> would

>> have wanted me to share Breanns current situation. If Joyce would

> have

>> known about Dr. Mehtas Early Treatment Method, she would have

> pursued it

>> for her daughter and odds are that Breann wouldnt be suffering... I

>> realize that each and every child with scoliosis is different, but

> Breanns

>> case was diagnosed at 29 degrees, under 1 yr. of age…….She would

> have

>> benefitted greatly from Dr. Mehtas ET Method. Again, this

> story is

>> not to scare you. This is reality for children suffering with

> severe

>> scoliosis, who didn't have the ET option 8/9 years ago…..Please

> send your

>> strength and good thoughts to our girl Breann and her family.

>> HRH

>>

>

>

>

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The kids also start next week. We should get together nest week on

Thursday, Friday, or Saturday. I will come down this week and bring

those to you. Maybe friday if that is good for you.

Rochelle

> >>

> >> I am sure that many of you have read Breanns Story on

> >> www.infantilescoliosis.org Breann and Olivia have followed

> > eachother on

> >> this scoliosis journey, since they were 2 & 3 years old (they are

> > now 10 &

> >> 11). The Veptr didnt work out for Breann like everyone had

hoped,

> > and

> >> last week it was decided that the best plan of action would be to

> > remove

> >> it. Last December 07, her left Veptr rod (dual hybrid attached

to

> > her

> >> pelvic structure) was removed, and she was placed in a brace.

Last

> > week,

> >> the right Veptr rod was removed, an anterior release was

performed,

> > 5

> >> disks were removed, a rib was removed, and she was placed into a

> > halo.

> >> All of this, to prepare for her definitive spinal fusion in 3 to

6

> > weeks.

> >> As you can imagine, she is having a difficult recovery and

enduring

> > a lot

> >> of pain. I am sharing this story in hopes that it will help

> > someone new

> >> on this forum to understand the importance of Early Treatment for

> >> progressive infantile scoliosis. Infants diagnosed with the

> > progressive

> >> form of scoliosis do not have time to wait and watch. ET has the

> > ability

> >> to rid them of the deformity, gently & permanently, if applied

> > properly.

> >> ET can prevent them from living a life full of surgeries, a

> > deformity ,

> >> pulmonary issues & pain. There is a window of time that

> > infants/children

> >> can benefit from the Early Treatment Method, so learn as much as

> > you can

> >> about this method, and scoliosis, and take action now. The ISOP

> > website

> >> was dedicated to Breanns mum Joyce back in 02, and I know that

she

> > would

> >> have wanted me to share Breanns current situation. If Joyce

would

> > have

> >> known about Dr. Mehtas Early Treatment Method, she would have

> > pursued it

> >> for her daughter and odds are that Breann wouldnt be

suffering... I

> >> realize that each and every child with scoliosis is different,

but

> > Breanns

> >> case was diagnosed at 29 degrees, under 1 yr. of age…….She would

> > have

> >> benefitted greatly from Dr. Mehtas ET Method. Again, this

> > story is

> >> not to scare you. This is reality for children suffering with

> > severe

> >> scoliosis, who didn't have the ET option 8/9 years ago…..Please

> > send your

> >> strength and good thoughts to our girl Breann and her family.

> >> HRH

> >>

> >

> >

> >

>

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Guest guest

I think Friday will work....My brother will be here at the office at

approx. 2:30 p.m. (Olivias school and my office are in the same

building). He is going to speak to Livs class about determination,

following your dream, etc.... and is picking her up in his new, tour bus.

She is ~SO~ excited!!! If you and are here, you can meet him.

Lets talk tomorrrow.

HRH

> The kids also start next week. We should get together nest week on

> Thursday, Friday, or Saturday. I will come down this week and bring

> those to you. Maybe friday if that is good for you.

> Rochelle

>

>

>

>> >>

>> >> I am sure that many of you have read Breanns Story on

>> >> www.infantilescoliosis.org Breann and Olivia have followed

>> > eachother on

>> >> this scoliosis journey, since they were 2 & 3 years old (they are

>> > now 10 &

>> >> 11). The Veptr didnt work out for Breann like everyone had

> hoped,

>> > and

>> >> last week it was decided that the best plan of action would be to

>> > remove

>> >> it. Last December 07, her left Veptr rod (dual hybrid attached

> to

>> > her

>> >> pelvic structure) was removed, and she was placed in a brace.

> Last

>> > week,

>> >> the right Veptr rod was removed, an anterior release was

> performed,

>> > 5

>> >> disks were removed, a rib was removed, and she was placed into a

>> > halo.

>> >> All of this, to prepare for her definitive spinal fusion in 3 to

> 6

>> > weeks.

>> >> As you can imagine, she is having a difficult recovery and

> enduring

>> > a lot

>> >> of pain. I am sharing this story in hopes that it will help

>> > someone new

>> >> on this forum to understand the importance of Early Treatment for

>> >> progressive infantile scoliosis. Infants diagnosed with the

>> > progressive

>> >> form of scoliosis do not have time to wait and watch. ET has the

>> > ability

>> >> to rid them of the deformity, gently & permanently, if applied

>> > properly.

>> >> ET can prevent them from living a life full of surgeries, a

>> > deformity ,

>> >> pulmonary issues & pain. There is a window of time that

>> > infants/children

>> >> can benefit from the Early Treatment Method, so learn as much as

>> > you can

>> >> about this method, and scoliosis, and take action now. The ISOP

>> > website

>> >> was dedicated to Breanns mum Joyce back in 02, and I know that

> she

>> > would

>> >> have wanted me to share Breanns current situation. If Joyce

> would

>> > have

>> >> known about Dr. Mehtas Early Treatment Method, she would have

>> > pursued it

>> >> for her daughter and odds are that Breann wouldnt be

> suffering... I

>> >> realize that each and every child with scoliosis is different,

> but

>> > Breanns

>> >> case was diagnosed at 29 degrees, under 1 yr. of age…….She would

>> > have

>> >> benefitted greatly from Dr. Mehtas ET Method. Again, this

>> > story is

>> >> not to scare you. This is reality for children suffering with

>> > severe

>> >> scoliosis, who didn't have the ET option 8/9 years ago…..Please

>> > send your

>> >> strength and good thoughts to our girl Breann and her family.

>> >> HRH

>> >>

>> >

>> >

>> >

>>

>

>

>

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!!

That is amazingly cool!

Shellie

heather@... wrote:

I think Friday will work....My brother will be here at the office at

approx. 2:30 p.m. (Olivias school and my office are in the same

building). He is going to speak to Livs class about determination,

following your dream, etc.... and is picking her up in his new, tour bus.

She is ~SO~ excited!!! If you and are here, you can meet him.

Lets talk tomorrrow.

HRH

> The kids also start next week. We should get together nest week on

> Thursday, Friday, or Saturday. I will come down this week and bring

> those to you. Maybe friday if that is good for you.

> Rochelle

>

>

>

>> >>

>> >> I am sure that many of you have read Breanns Story on

>> >> www.infantilescoliosis.org Breann and Olivia have followed

>> > eachother on

>> >> this scoliosis journey, since they were 2 & 3 years old (they are

>> > now 10 &

>> >> 11). The Veptr didnt work out for Breann like everyone had

> hoped,

>> > and

>> >> last week it was decided that the best plan of action would be to

>> > remove

>> >> it. Last December 07, her left Veptr rod (dual hybrid attached

> to

>> > her

>> >> pelvic structure) was removed, and she was placed in a brace.

> Last

>> > week,

>> >> the right Veptr rod was removed, an anterior release was

> performed,

>> > 5

>> >> disks were removed, a rib was removed, and she was placed into a

>> > halo.

>> >> All of this, to prepare for her definitive spinal fusion in 3 to

> 6

>> > weeks.

>> >> As you can imagine, she is having a difficult recovery and

> enduring

>> > a lot

>> >> of pain. I am sharing this story in hopes that it will help

>> > someone new

>> >> on this forum to understand the importance of Early Treatment for

>> >> progressive infantile scoliosis. Infants diagnosed with the

>> > progressive

>> >> form of scoliosis do not have time to wait and watch. ET has the

>> > ability

>> >> to rid them of the deformity, gently & permanently, if applied

>> > properly.

>> >> ET can prevent them from living a life full of surgeries, a

>> > deformity ,

>> >> pulmonary issues & pain. There is a window of time that

>> > infants/children

>> >> can benefit from the Early Treatment Method, so learn as much as

>> > you can

>> >> about this method, and scoliosis, and take action now. The ISOP

>> > website

>> >> was dedicated to Breanns mum Joyce back in 02, and I know that

> she

>> > would

>> >> have wanted me to share Breanns current situation. If Joyce

> would

>> > have

>> >> known about Dr. Mehtas Early Treatment Method, she would have

>> > pursued it

>> >> for her daughter and odds are that Breann wouldnt be

> suffering... I

>> >> realize that each and every child with scoliosis is different,

> but

>> > Breanns

>> >> case was diagnosed at 29 degrees, under 1 yr. of age…….She would

>> > have

>> >> benefitted greatly from Dr. Mehtas ET Method. Again, this

>> > story is

>> >> not to scare you. This is reality for children suffering with

>> > severe

>> >> scoliosis, who didn't have the ET option 8/9 years ago…..Please

>> > send your

>> >> strength and good thoughts to our girl Breann and her family.

>> >> HRH

>> >>

>> >

>> >

>> >

>>

>

>

>

---------------------------------

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Guest guest

That sounds like such a blast for everyone involved!

Gail

Shellie Grant wrote:

!!

That is amazingly cool!

Shellie

heather@... wrote:

I think Friday will work....My brother will be here at the office at

approx. 2:30 p.m. (Olivias school and my office are in the same

building). He is going to speak to Livs class about determination,

following your dream, etc.... and is picking her up in his new, tour bus.

She is ~SO~ excited!!! If you and are here, you can meet him.

Lets talk tomorrrow.

HRH

> The kids also start next week. We should get together nest week on

> Thursday, Friday, or Saturday. I will come down this week and bring

> those to you. Maybe friday if that is good for you.

> Rochelle

>

>

>

>> >>

>> >> I am sure that many of you have read Breanns Story on

>> >> www.infantilescoliosis.org Breann and Olivia have followed

>> > eachother on

>> >> this scoliosis journey, since they were 2 & 3 years old (they are

>> > now 10 &

>> >> 11). The Veptr didnt work out for Breann like everyone had

> hoped,

>> > and

>> >> last week it was decided that the best plan of action would be to

>> > remove

>> >> it. Last December 07, her left Veptr rod (dual hybrid attached

> to

>> > her

>> >> pelvic structure) was removed, and she was placed in a brace.

> Last

>> > week,

>> >> the right Veptr rod was removed, an anterior release was

> performed,

>> > 5

>> >> disks were removed, a rib was removed, and she was placed into a

>> > halo.

>> >> All of this, to prepare for her definitive spinal fusion in 3 to

> 6

>> > weeks.

>> >> As you can imagine, she is having a difficult recovery and

> enduring

>> > a lot

>> >> of pain. I am sharing this story in hopes that it will help

>> > someone new

>> >> on this forum to understand the importance of Early Treatment for

>> >> progressive infantile scoliosis. Infants diagnosed with the

>> > progressive

>> >> form of scoliosis do not have time to wait and watch. ET has the

>> > ability

>> >> to rid them of the deformity, gently & permanently, if applied

>> > properly.

>> >> ET can prevent them from living a life full of surgeries, a

>> > deformity ,

>> >> pulmonary issues & pain. There is a window of time that

>> > infants/children

>> >> can benefit from the Early Treatment Method, so learn as much as

>> > you can

>> >> about this method, and scoliosis, and take action now. The ISOP

>> > website

>> >> was dedicated to Breanns mum Joyce back in 02, and I know that

> she

>> > would

>> >> have wanted me to share Breanns current situation. If Joyce

> would

>> > have

>> >> known about Dr. Mehtas Early Treatment Method, she would have

>> > pursued it

>> >> for her daughter and odds are that Breann wouldnt be

> suffering... I

>> >> realize that each and every child with scoliosis is different,

> but

>> > Breanns

>> >> case was diagnosed at 29 degrees, under 1 yr. of age…….She would

>> > have

>> >> benefitted greatly from Dr. Mehtas ET Method. Again, this

>> > story is

>> >> not to scare you. This is reality for children suffering with

>> > severe

>> >> scoliosis, who didn't have the ET option 8/9 years ago…..Please

>> > send your

>> >> strength and good thoughts to our girl Breann and her family.

>> >> HRH

>> >>

>> >

>> >

>> >

>>

>

>

>

---------------------------------

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Guest guest

Sounds good I will give you a call tomorrow afternoon. That will

be so fun for Liv.

Rochelle

> >> >>

> >> >> I am sure that many of you have read Breanns Story on

> >> >> www.infantilescoliosis.org Breann and Olivia have followed

> >> > eachother on

> >> >> this scoliosis journey, since they were 2 & 3 years old (they

are

> >> > now 10 &

> >> >> 11). The Veptr didnt work out for Breann like everyone had

> > hoped,

> >> > and

> >> >> last week it was decided that the best plan of action would

be to

> >> > remove

> >> >> it. Last December 07, her left Veptr rod (dual hybrid

attached

> > to

> >> > her

> >> >> pelvic structure) was removed, and she was placed in a brace.

> > Last

> >> > week,

> >> >> the right Veptr rod was removed, an anterior release was

> > performed,

> >> > 5

> >> >> disks were removed, a rib was removed, and she was placed

into a

> >> > halo.

> >> >> All of this, to prepare for her definitive spinal fusion in 3

to

> > 6

> >> > weeks.

> >> >> As you can imagine, she is having a difficult recovery and

> > enduring

> >> > a lot

> >> >> of pain. I am sharing this story in hopes that it will help

> >> > someone new

> >> >> on this forum to understand the importance of Early Treatment

for

> >> >> progressive infantile scoliosis. Infants diagnosed with the

> >> > progressive

> >> >> form of scoliosis do not have time to wait and watch. ET has

the

> >> > ability

> >> >> to rid them of the deformity, gently & permanently, if applied

> >> > properly.

> >> >> ET can prevent them from living a life full of surgeries, a

> >> > deformity ,

> >> >> pulmonary issues & pain. There is a window of time that

> >> > infants/children

> >> >> can benefit from the Early Treatment Method, so learn as much

as

> >> > you can

> >> >> about this method, and scoliosis, and take action now. The

ISOP

> >> > website

> >> >> was dedicated to Breanns mum Joyce back in 02, and I know that

> > she

> >> > would

> >> >> have wanted me to share Breanns current situation. If Joyce

> > would

> >> > have

> >> >> known about Dr. Mehtas Early Treatment Method, she would have

> >> > pursued it

> >> >> for her daughter and odds are that Breann wouldnt be

> > suffering... I

> >> >> realize that each and every child with scoliosis is different,

> > but

> >> > Breanns

> >> >> case was diagnosed at 29 degrees, under 1 yr. of age…….She

would

> >> > have

> >> >> benefitted greatly from Dr. Mehtas ET Method. Again, this

> >> > story is

> >> >> not to scare you. This is reality for children suffering

with

> >> > severe

> >> >> scoliosis, who didn't have the ET option 8/9 years

ago…..Please

> >> > send your

> >> >> strength and good thoughts to our girl Breann and her family.

> >> >> HRH

> >> >>

> >> >

> >> >

> >> >

> >>

> >

> >

> >

>

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