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That is great that people see her for herself and not as a child with scoliosis.

I am so happy for her...I know it's been such a long road.

Noelle (12-2-01)

Ian (8-15-04)

Olivia

I wanted to share something that's been happening over the last year, that I

hadnt really figured out, until yesterday. As most of you know, Olivia has

been in casts, braces all of her life. Last year, she underwent her 1st

surgical procedure(veptr dual rods attached to her pelvic structure) because

she had come to the end of the road in casts and braces.

A month ago, Olivia told me that she did not like her teacher, because he

didnt pay attention to her! Well, this really upset me.....I didnt take

action, because I had to think about it for a while. The teacher seems like

a really good, caring, guy....There had to be something else going

on.....Well, I think I just figured it out.

Olivia is used to getting just a little more attention from people, due to

her very obvious casts and braces (w/ neck support)....Now, that she no

longer wears them, she doesnt stand out as much, and the attention she used

to recieve is less. She is just like the other kids...No one even notices

her scoliosis. I think I am so excited about this, because to everyone at

her school, she is Olivia... Not Olivia with scoliosis. This means a lot

to a 9 year old girl, who is growing up and wanting to fit in and be like

the rest.

Very young children with scoliosis, dont care what others think. They

usually take their cues from their parents, and how the parents feel about

it. Little ones can be taught to take pride in their casts and braces. I

look back on it, and that was the easy time. No questions, no feelings of

being left out, no worries about ~not~ looking exactly like the other kids,

sad because she cant keep up, etc.....I am 100% convinced that Olivia looks

so good, because she did wear casts for so long, and over the years they

improved her overall body shape. ( Remember, her curves were over 100).

Anyway, sorry about the ramble. I am just relieved that Olivia isnt starved

for attention. She is just used to getting a lot. Now, she is just one of

the kids. She can choose to work harder to get the attention, or

not....Just like any other kid.

One more thing that I have to share. Apparently, the teacher had a few

minutes of free time after lunch yesterday, and he decided to have a contest

to see who could hold their breath the longest. Guess who won?!! (out of 45

kids) Olivia!! Not bad for 76% lung function, heh? She won a pencil. This

makes me a true believer of the bi-pap breathing exersizes she has been

doing since age 2. I feel like we are very lucky, and I am very grateful

for my childs health. I know what Livs life could have been, and we are

nowhere near that place! Not today, anyway!

Thanks for listening.

HRH

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Hi ,

Thank you for sharing this experience. It is wonderful to hear about Olivia.

Someday, if she doesn't already know, she will find out how her life, courage,

strength, story, and the tenacity of her mother, have helped so many people.

Team Olivia!!

Love,

Raegan 3, 16 mo.

Olivia

I wanted to share something that's been happening over the last year, that I

hadnt really figured out, until yesterday. As most of you know, Olivia has

been in casts, braces all of her life. Last year, she underwent her 1st

surgical procedure(veptr dual rods attached to her pelvic structure) because

she had come to the end of the road in casts and braces.

A month ago, Olivia told me that she did not like her teacher, because he

didnt pay attention to her! Well, this really upset me.....I didnt take

action, because I had to think about it for a while. The teacher seems like

a really good, caring, guy....There had to be something else going

on.....Well, I think I just figured it out.

Olivia is used to getting just a little more attention from people, due to

her very obvious casts and braces (w/ neck support).... Now, that she no

longer wears them, she doesnt stand out as much, and the attention she used

to recieve is less. She is just like the other kids...No one even notices

her scoliosis. I think I am so excited about this, because to everyone at

her school, she is Olivia... Not Olivia with scoliosis. This means a lot

to a 9 year old girl, who is growing up and wanting to fit in and be like

the rest.

Very young children with scoliosis, dont care what others think. They

usually take their cues from their parents, and how the parents feel about

it. Little ones can be taught to take pride in their casts and braces. I

look back on it, and that was the easy time. No questions, no feelings of

being left out, no worries about ~not~ looking exactly like the other kids,

sad because she cant keep up, etc.....I am 100% convinced that Olivia looks

so good, because she did wear casts for so long, and over the years they

improved her overall body shape. ( Remember, her curves were over 100).

Anyway, sorry about the ramble. I am just relieved that Olivia isnt starved

for attention. She is just used to getting a lot. Now, she is just one of

the kids. She can choose to work harder to get the attention, or

not....Just like any other kid.

One more thing that I have to share. Apparently, the teacher had a few

minutes of free time after lunch yesterday, and he decided to have a contest

to see who could hold their breath the longest. Guess who won?!! (out of 45

kids) Olivia!! Not bad for 76% lung function, heh? She won a pencil. This

makes me a true believer of the bi-pap breathing exersizes she has been

doing since age 2. I feel like we are very lucky, and I am very grateful

for my childs health. I know what Livs life could have been, and we are

nowhere near that place! Not today, anyway!

Thanks for listening.

HRH

________________________________________________________________________________\

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Guest guest

How wonderful! You and Olivia are true angels.....

Tyler 4

Matson 12 months dx 12/06

Lily 1 month

>

> Hi ,

> Thank you for sharing this experience. It is wonderful to hear

about Olivia. Someday, if she doesn't already know, she will find out

how her life, courage, strength, story, and the tenacity of her

mother, have helped so many people. Team Olivia!!

> Love,

> Raegan 3, 16 mo.

>

>

> Olivia

>

> I wanted to share something that's been happening over the last

year, that I

> hadnt really figured out, until yesterday. As most of you know,

Olivia has

> been in casts, braces all of her life. Last year, she underwent her

1st

> surgical procedure(veptr dual rods attached to her pelvic

structure) because

> she had come to the end of the road in casts and braces.

> A month ago, Olivia told me that she did not like her teacher,

because he

> didnt pay attention to her! Well, this really upset me.....I didnt

take

> action, because I had to think about it for a while. The teacher

seems like

> a really good, caring, guy....There had to be something else going

> on.....Well, I think I just figured it out.

> Olivia is used to getting just a little more attention from people,

due to

> her very obvious casts and braces (w/ neck support).... Now, that

she no

> longer wears them, she doesnt stand out as much, and the attention

she used

> to recieve is less. She is just like the other kids...No one even

notices

> her scoliosis. I think I am so excited about this, because to

everyone at

> her school, she is Olivia... Not Olivia with scoliosis. This means

a lot

> to a 9 year old girl, who is growing up and wanting to fit in and

be like

> the rest.

> Very young children with scoliosis, dont care what others think.

They

> usually take their cues from their parents, and how the parents

feel about

> it. Little ones can be taught to take pride in their casts and

braces. I

> look back on it, and that was the easy time. No questions, no

feelings of

> being left out, no worries about ~not~ looking exactly like the

other kids,

> sad because she cant keep up, etc.....I am 100% convinced that

Olivia looks

> so good, because she did wear casts for so long, and over the years

they

> improved her overall body shape. ( Remember, her curves were over

100).

> Anyway, sorry about the ramble. I am just relieved that Olivia isnt

starved

> for attention. She is just used to getting a lot. Now, she is just

one of

> the kids. She can choose to work harder to get the attention, or

> not....Just like any other kid.

> One more thing that I have to share. Apparently, the teacher had a

few

> minutes of free time after lunch yesterday, and he decided to have

a contest

> to see who could hold their breath the longest. Guess who won?!!

(out of 45

> kids) Olivia!! Not bad for 76% lung function, heh? She won a

pencil. This

> makes me a true believer of the bi-pap breathing exersizes she has

been

> doing since age 2. I feel like we are very lucky, and I am very

grateful

> for my childs health. I know what Livs life could have been, and we

are

> nowhere near that place! Not today, anyway!

>

> Thanks for listening.

>

> HRH

>

>

>

>

>

>

>

______________________________________________________________________

______________

> Sucker-punch spam with award-winning protection.

> Try the free Beta.

> http://advision.webevents./mailbeta/features_spam.html

>

>

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Guest guest

How wonderful! You and Olivia are true angels.....

Tyler 4

Matson 12 months dx 12/06

Lily 1 month

>

> Hi ,

> Thank you for sharing this experience. It is wonderful to hear

about Olivia. Someday, if she doesn't already know, she will find out

how her life, courage, strength, story, and the tenacity of her

mother, have helped so many people. Team Olivia!!

> Love,

> Raegan 3, 16 mo.

>

>

> Olivia

>

> I wanted to share something that's been happening over the last

year, that I

> hadnt really figured out, until yesterday. As most of you know,

Olivia has

> been in casts, braces all of her life. Last year, she underwent her

1st

> surgical procedure(veptr dual rods attached to her pelvic

structure) because

> she had come to the end of the road in casts and braces.

> A month ago, Olivia told me that she did not like her teacher,

because he

> didnt pay attention to her! Well, this really upset me.....I didnt

take

> action, because I had to think about it for a while. The teacher

seems like

> a really good, caring, guy....There had to be something else going

> on.....Well, I think I just figured it out.

> Olivia is used to getting just a little more attention from people,

due to

> her very obvious casts and braces (w/ neck support).... Now, that

she no

> longer wears them, she doesnt stand out as much, and the attention

she used

> to recieve is less. She is just like the other kids...No one even

notices

> her scoliosis. I think I am so excited about this, because to

everyone at

> her school, she is Olivia... Not Olivia with scoliosis. This means

a lot

> to a 9 year old girl, who is growing up and wanting to fit in and

be like

> the rest.

> Very young children with scoliosis, dont care what others think.

They

> usually take their cues from their parents, and how the parents

feel about

> it. Little ones can be taught to take pride in their casts and

braces. I

> look back on it, and that was the easy time. No questions, no

feelings of

> being left out, no worries about ~not~ looking exactly like the

other kids,

> sad because she cant keep up, etc.....I am 100% convinced that

Olivia looks

> so good, because she did wear casts for so long, and over the years

they

> improved her overall body shape. ( Remember, her curves were over

100).

> Anyway, sorry about the ramble. I am just relieved that Olivia isnt

starved

> for attention. She is just used to getting a lot. Now, she is just

one of

> the kids. She can choose to work harder to get the attention, or

> not....Just like any other kid.

> One more thing that I have to share. Apparently, the teacher had a

few

> minutes of free time after lunch yesterday, and he decided to have

a contest

> to see who could hold their breath the longest. Guess who won?!!

(out of 45

> kids) Olivia!! Not bad for 76% lung function, heh? She won a

pencil. This

> makes me a true believer of the bi-pap breathing exersizes she has

been

> doing since age 2. I feel like we are very lucky, and I am very

grateful

> for my childs health. I know what Livs life could have been, and we

are

> nowhere near that place! Not today, anyway!

>

> Thanks for listening.

>

> HRH

>

>

>

>

>

>

>

______________________________________________________________________

______________

> Sucker-punch spam with award-winning protection.

> Try the free Beta.

> http://advision.webevents./mailbeta/features_spam.html

>

>

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  • 2 weeks later...
Guest guest

-,

We are praying and thinking of you and Olivia. We hope everything

goes well in SLC on Wednesday.

Many prayers,

and Matt

Tyler 4

Matson 13 months (dx Dec 06)

Lily 7 weeks

-- In infantile scoliosis treatment , " heather hyatt "

wrote:

>

> I sent this e-mail earlier, but dont see it coming through.....

> Again...

> Olivias veptr rods are migrating. The rods are protruding

significantly, at

> the shoulders. I think there may be some rib breakage at the top

anchoring

> points, but she shows no signs of pain...(?) We are headed to SLC,

on Weds.

>

> Please pray for my girl.

>

> HRH

>

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Guest guest

Good luck and Olivia. As always, prayers and thoughts with you. Olivia

is such a brave girl!

/Cole

heather hyatt wrote:

I sent this e-mail earlier, but dont see it coming through.....

Again...

Olivias veptr rods are migrating. The rods are protruding significantly, at

the shoulders. I think there may be some rib breakage at the top anchoring

points, but she shows no signs of pain...(?) We are headed to SLC, on Weds.

Please pray for my girl.

HRH

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

No need to miss a message. Get email on-the-go

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Thanks .

Thanks .

If my daughters ribs are broken, I will work harder than ever before in trying

to make Early Treatment a primary option for infants/children with progressive

infantile scoliosis!!! No child/family should have to go through this. 9 years

ago early treatment was not an option, but today it should be offered at every

hospital. Families should have the Early Treatment option, ~before~ any surgery

is recommended.

HRH

Re: Olivia

-,

We are praying and thinking of you and Olivia. We hope everything

goes well in SLC on Wednesday.

Many prayers,

and Matt

Tyler 4

Matson 13 months (dx Dec 06)

Lily 7 weeks

-- In infantile scoliosis treatment , " heather hyatt "

wrote:

>

> I sent this e-mail earlier, but dont see it coming through.....

> Again...

> Olivias veptr rods are migrating. The rods are protruding

significantly, at

> the shoulders. I think there may be some rib breakage at the top

anchoring

> points, but she shows no signs of pain...(?) We are headed to SLC,

on Weds.

>

> Please pray for my girl.

>

> HRH

>

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Guest guest

,

Of course.............I will be praying for Olivia.

Let us know how things go.

Tasha

heather hyatt wrote:

I sent this e-mail earlier, but dont see it coming through.....

Again...

Olivias veptr rods are migrating. The rods are protruding significantly, at

the shoulders. I think there may be some rib breakage at the top anchoring

points, but she shows no signs of pain...(?) We are headed to SLC, on Weds.

Please pray for my girl.

HRH

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

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Guest guest

,

Give Olivia a gentle hug from us. Call me when you

get to town. I'll be in SLC on Friday. Braydon's

VEPTR has migrated too, but in a very different

fashion, I'm guessing. In Braydon's case, the

migration has been a slow process, not causing any

discomfort or problem with the natural ribs. The

migration through the ribs sounds much worse than it

is. I promise. Take care!

Carmell

Mom to Kara, idiopathic scoliosis and hypothyroidism, Blake 16, GERD, and

Braydon 11, VACTERL-congenital scoliosis (fusion surgery 5/96), VEPTR patient

#137 (implant 8/01), Thoracic Insufficiency Syndrome (TIS), rib anomalies,

missing coccyx, fatty filum/TC (released 4/99 & 12/06), anal stenosis, chronic

constipation, horseshoe (cross-fused) kidney, dbl ureter in left kidney,

ureterocele (excized 6/95), kidney reflux (reimplant surgery 1/97), neurogenic

bladder, dysplastic right leg w/right clubfoot with 8 toes (repaired 2/96, 3/96,

1/97, 3/04), tibial torsion, 4cm length discrepancy-wears 3cm lift, pes cavus,

SUA, GERD, Gastroparesis, etc. http://carmellb-ivil.tripod.com/myfamily/

Congenital scoliosis support group

http://health./group/CongenitalScoliosisSupport/

________________________________________________________________________________\

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Guest guest

,

I hope all is well with Olivia. She's a tough cookie that's for sure. I will

keep my fingers crossed that all goes well.

Noelle (12-2-01)

Ian (8-15-04)

Olivia

I sent this e-mail earlier, but dont see it coming through.....

Again...

Olivias veptr rods are migrating. The rods are protruding significantly, at

the shoulders. I think there may be some rib breakage at the top anchoring

points, but she shows no signs of pain...(?) We are headed to SLC, on Weds.

Please pray for my girl.

HRH

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Guest guest

heather,

of course, my prayers are with you and olivia. good luck with your

appointment. i hope you get some good news. she deserves it!

my best,

deshea

> I sent this e-mail earlier, but dont see it coming through.....

> Again...

> Olivias veptr rods are migrating. The rods are protruding

> significantly, at

> the shoulders. I think there may be some rib breakage at the top

> anchoring

> points, but she shows no signs of pain...(?) We are headed to SLC,

> on Weds.

>

> Please pray for my girl.

>

> HRH

>

>

>

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Guest guest

,

Olivia is in our thoughts and our prayers. You're right-on a postive

note-she's not in pain or discomfort. Hope all goes well on

wednesday.

Good Luck,

Aekta, Dave & Maxwell

>

> I sent this e-mail earlier, but dont see it coming through.....

> Again...

> Olivias veptr rods are migrating. The rods are protruding

significantly, at

> the shoulders. I think there may be some rib breakage at the top

anchoring

> points, but she shows no signs of pain...(?) We are headed to

SLC, on Weds.

>

> Please pray for my girl.

>

> HRH

>

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Guest guest

Our thoughts and prayers are with you and Olivia. We look forward to hearing

from you when you return.

Love,

and

Raegan 3yrs 17 months

Olivia

I sent this e-mail earlier, but dont see it coming through.....

Again...

Olivias veptr rods are migrating. The rods are protruding significantly, at

the shoulders. I think there may be some rib breakage at the top anchoring

points, but she shows no signs of pain...(?) We are headed to SLC, on Weds.

Please pray for my girl.

HRH

________________________________________________________________________________\

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Guest guest

Good luck and Olivia

We wish you all the best and hope for good results and better results than you

are expecting..

We will be sending prayers

Love Bert and Bridget

heather hyatt wrote:

I sent this e-mail earlier, but dont see it coming through.....

Again...

Olivias veptr rods are migrating. The rods are protruding significantly, at

the shoulders. I think there may be some rib breakage at the top anchoring

points, but she shows no signs of pain...(?) We are headed to SLC, on Weds.

Please pray for my girl.

HRH

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

Get your own web address.

Have a HUGE year through Yahoo! Small Business.

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Guest guest

,

You are in our family's prayers as always. I am so sorry you have to go through

all of this!

You are such a strength for you daughter. I admire your dedication and ambition

on her

behalf. Good luck and keep us updated!!!

Hansen

>

> I sent this e-mail earlier, but dont see it coming through.....

> Again...

> Olivias veptr rods are migrating. The rods are protruding significantly, at

> the shoulders. I think there may be some rib breakage at the top anchoring

> points, but she shows no signs of pain...(?) We are headed to SLC, on Weds.

>

> Please pray for my girl.

>

> HRH

>

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Guest guest

,

She's in our prayers. Take care.

Jerry

Olivia

I sent this e-mail earlier, but dont see it coming through.....

Again...

Olivias veptr rods are migrating. The rods are protruding significantly, at

the shoulders. I think there may be some rib breakage at the top anchoring

points, but she shows no signs of pain...(?) We are headed to SLC, on Weds.

Please pray for my girl.

HRH

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Guest guest

,

You are in our prayers. Hope everything goes well in SLC.

tried to call Monday night to let you know I Recieved the article

thank you. Devyn's surgery for the Chiari is scheduled for next

thursday the 29th at Denver childrens. They have said we will have to

wait till june now to cast. Again good luck and hope to talk to you

when you return.

Rochelle West

>

> I sent this e-mail earlier, but dont see it coming through.....

> Again...

> Olivias veptr rods are migrating. The rods are protruding

significantly, at

> the shoulders. I think there may be some rib breakage at the top

anchoring

> points, but she shows no signs of pain...(?) We are headed to SLC,

on Weds.

>

> Please pray for my girl.

>

> HRH

>

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Guest guest

,

We are praying for you both! Please take Care.

Amy & Adelaide

heather hyatt wrote:

Thanks .

Thanks .

If my daughters ribs are broken, I will work harder than ever before in trying

to make Early Treatment a primary option for infants/children with progressive

infantile scoliosis!!! No child/family should have to go through this. 9 years

ago early treatment was not an option, but today it should be offered at every

hospital. Families should have the Early Treatment option, ~before~ any surgery

is recommended.

HRH

Re: Olivia

-,

We are praying and thinking of you and Olivia. We hope everything

goes well in SLC on Wednesday.

Many prayers,

and Matt

Tyler 4

Matson 13 months (dx Dec 06)

Lily 7 weeks

-- In infantile scoliosis treatment , " heather hyatt "

wrote:

>

> I sent this e-mail earlier, but dont see it coming through.....

> Again...

> Olivias veptr rods are migrating. The rods are protruding

significantly, at

> the shoulders. I think there may be some rib breakage at the top

anchoring

> points, but she shows no signs of pain...(?) We are headed to SLC,

on Weds.

>

> Please pray for my girl.

>

> HRH

>

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Guest guest

We wish you every luck and success. I can only imagine how worried you are!

Glad Oliviia isn't phased! xoxox Abigail and Nadia

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

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Guest guest

-

Good luck to you guys

I have a thought about broken ribs....You said she was not in pain so

maybe there aren't any broken ribs ......would'nt she be in same pain

so maybe that is a good note?

Keep us posted and good luck

and Adan

-- In infantile scoliosis treatment , Amy Norenberg

wrote:

>

> ,

> We are praying for you both! Please take Care.

> Amy & Adelaide

>

> heather hyatt wrote:

> Thanks .

> Thanks .

> If my daughters ribs are broken, I will work harder than ever

before in trying to make Early Treatment a primary option for

infants/children with progressive infantile scoliosis!!! No

child/family should have to go through this. 9 years ago early

treatment was not an option, but today it should be offered at every

hospital. Families should have the Early Treatment option, ~before~

any surgery is recommended.

>

> HRH

> Re: Olivia

>

> -,

> We are praying and thinking of you and Olivia. We hope everything

> goes well in SLC on Wednesday.

> Many prayers,

> and Matt

> Tyler 4

> Matson 13 months (dx Dec 06)

> Lily 7 weeks

>

> -- In infantile scoliosis treatment , " heather hyatt "

> <heather@> wrote:

> >

> > I sent this e-mail earlier, but dont see it coming through.....

> > Again...

> > Olivias veptr rods are migrating. The rods are protruding

> significantly, at

> > the shoulders. I think there may be some rib breakage at the top

> anchoring

> > points, but she shows no signs of pain...(?) We are headed to

SLC,

> on Weds.

> >

> > Please pray for my girl.

> >

> > HRH

> >

>

>

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Guest guest

Sending again....

Re: called re: Olivia

HI Everyone,

Shellie here. called me this evening with an update. All those prayers

were heard, because Olivia is fine. Her xrays show that the Veptrs are fine and

NO ribs are broken. The protrusion is actually an area of fluid between layers

of skin. They are going to take care of that tomorrow and do a mini-expansion of

the Veptrs. Mini, because they need to keep an eye on the area. Mini also (as

opposed to not expanding) because if you wait too long between expansions some

spines become rigid. is very relieved and thanks everyone for thinking

of her and Olivia. She will call me again tomorrow with another update on how

things go.

Shellie

heather hyatt wrote:

Thanks for all of your positive thoughts and prayers. We leave first thing

in the a.m., and should be to SLC before evryone gets to work (LOL)!!

Olivia is doing great, and doesnt even realize my concern. Dont want to

scare her.

I'll have Shellie post for us, when we figure out whats going on.

Love,

HRH

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Guest guest

,

Glad to hear your are home and getting ready for a

FABULOUS trip! You both could use some time away from

medical stress and trauma to ENJOY life! Good for

you. I wish I would have called you while you were

here... I know how worried you were, but glad it

wasn't as serious as you thought. Braydon has quite a

large bursa over the bottom part of his chestwall

device. They've drained it a few times during routine

expansion surgeries, but it always comes back. Its

just how his body heals.

We'll be anxious to hear how your cruise goes, and how

the trip to VA goes, and so many adventures in your

life. Let me know if I can do anything to help.

Carmell

Mom to Kara, idiopathic scoliosis and hypothyroidism, Blake 16, GERD, and

Braydon 11, VACTERL-congenital scoliosis (fusion surgery 5/96), VEPTR patient

#137 (implant 8/01), Thoracic Insufficiency Syndrome (TIS), rib anomalies,

missing coccyx, fatty filum/TC (released 4/99 & 12/06), anal stenosis, chronic

constipation, horseshoe (cross-fused) kidney, dbl ureter in left kidney,

ureterocele (excized 6/95), kidney reflux (reimplant surgery 1/97), neurogenic

bladder, dysplastic right leg w/right clubfoot with 8 toes (repaired 2/96, 3/96,

1/97, 3/04), tibial torsion, 4cm length discrepancy-wears 3cm lift, pes cavus,

SUA, GERD, Gastroparesis, etc. http://carmellb-ivil.tripod.com/myfamily/

Congenital scoliosis support group

http://health./group/CongenitalScoliosisSupport/

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Great news and love to Olivia too from me and Bridget. Have a wonderful

trip and enjoy the ocean and the sand. Catch a wave for us..

Love Bert and Bridget

heather hyatt wrote:

Sending again....

Re: called re: Olivia

HI Everyone,

Shellie here. called me this evening with an update. All those prayers

were heard, because Olivia is fine. Her xrays show that the Veptrs are fine and

NO ribs are broken. The protrusion is actually an area of fluid between layers

of skin. They are going to take care of that tomorrow and do a mini-expansion of

the Veptrs. Mini, because they need to keep an eye on the area. Mini also (as

opposed to not expanding) because if you wait too long between expansions some

spines become rigid. is very relieved and thanks everyone for thinking

of her and Olivia. She will call me again tomorrow with another update on how

things go.

Shellie

heather hyatt wrote:

Thanks for all of your positive thoughts and prayers. We leave first thing

in the a.m., and should be to SLC before evryone gets to work (LOL)!!

Olivia is doing great, and doesnt even realize my concern. Dont want to

scare her.

I'll have Shellie post for us, when we figure out whats going on.

Love,

HRH

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I am really sorry that we didnt connect, Carmell. There was so much going on at

the hospital, I could barely take a break.

We were able to see Kylie, Bethany, & Breann this time, so Olivia really had

fun. This was the 1st time that Bethany and Liv were able to meet, and it was

great to see all of them " hanging out " together. They are all growing up into

amazing young women, who have a lot to do in this lifetime. I think that our

doc is going to try to schedule expansions for Breann & Liv together, which

makes all of our lives a lot easier....They both did great, and were walking

around by evening, right after the expansions..

That darn bursa almost gave me a heart attack! I was sick to my stomach last

week, thinking her rods had migrated through! The protrusion was significant,

and I would have never thought it to be a bursa. It made both rods protrude.

Anyway, we lucked out, again! I am so relieved.

All you can do is continue providing your solid experience on this group. You

know we all appreciate what you have to say, Carmell.

I'll be in touch, when we get home. Olivia is so excited about her wish, she

can hardly stand it. She has never seen the beach. She is trying to go to bed

early every night, so the next day will be here quicker! Now, thats exitement!

Thanks for recommending the M-A-W, and going to bat for us!!! This vacation has

been a long time coming, and we are beside ourselves. The limo will be here to

pick us up on Sat....Oh, and her best friend since kindergarden is coming with

us!!

Yeah!

HRH

Re: Fw: Olivia

,

Glad to hear your are home and getting ready for a

FABULOUS trip! You both could use some time away from

medical stress and trauma to ENJOY life! Good for

you. I wish I would have called you while you were

here... I know how worried you were, but glad it

wasn't as serious as you thought. Braydon has quite a

large bursa over the bottom part of his chestwall

device. They've drained it a few times during routine

expansion surgeries, but it always comes back. Its

just how his body heals.

We'll be anxious to hear how your cruise goes, and how

the trip to VA goes, and so many adventures in your

life. Let me know if I can do anything to help.

Carmell

Mom to Kara, idiopathic scoliosis and hypothyroidism, Blake 16, GERD, and

Braydon 11, VACTERL-congenital scoliosis (fusion surgery 5/96), VEPTR patient

#137 (implant 8/01), Thoracic Insufficiency Syndrome (TIS), rib anomalies,

missing coccyx, fatty filum/TC (released 4/99 & 12/06), anal stenosis, chronic

constipation, horseshoe (cross-fused) kidney, dbl ureter in left kidney,

ureterocele (excized 6/95), kidney reflux (reimplant surgery 1/97), neurogenic

bladder, dysplastic right leg w/right clubfoot with 8 toes (repaired 2/96, 3/96,

1/97, 3/04), tibial torsion, 4cm length discrepancy-wears 3cm lift, pes cavus,

SUA, GERD, Gastroparesis, etc. http://carmellb-ivil.tripod.com/myfamily/

Congenital scoliosis support group

http://health./group/CongenitalScoliosisSupport/

__________________________________________________________

Never miss an email again!

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“She is trying to go to bed early every night, so the next day will be here

quicker! Now, thats exitement!”

The real question is, is she even sleeping? Lol, If I was her and expecting

a trip like that, I would find it very hard to sleep besides doing anything

else.

Have a blast on this trip, you 2 deserve it.

Betty

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