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Old 07-18-2009, 03:17 PM
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saywhatyouwill saywhatyouwill is offline
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Default emily's LTR

the first stage went exactly as planned. her doctors are very pleased with it all. there is so much i could say but will try to keep this short!

mainly, i feel like an idiot for being so unprepared for how hard it would be on her. she spent all night crying even when she was asleep. i couldn't believe they started her on paracetamol and brufen only!! she's now getting dihydrocodeine as well. phew.

she has done well in lots of ways: they expected that she would be ventilated for at least several hours post op and maybe up to a week but she was off before she was out of recovery. she came off oxygen completely after 24 or so hours. she had her first tube change today and that went well too. and we are back on the ward and not in HDU which is very nice.

the 2 things they didn't tell us are among the worst!: she can't vocalise at all as her stent has been stitched over to stop any airflow, and she has to be NG fed for 7 days. she's being VERY good at trying not to pull at the tube. mummy, however, managed to yank it out by mistake today.

so...it's been agreed that whatever her airway looks like at the scope next week (and stent removal) we will come home for a bit with the trach just to get a break and head back in sometime later in the summer for decan.

:-D

very proud of her.
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*clare.
mum to emily
12/02/07 (placental abruption)
APGARS 0+1 (HIE gr.2/seizures) but she MADE IT! with the determination that we still see in her every day.
Grade III SGS - emergency tracheotomy July 2007.
2 stage LTR July 09 - DECANNED 27.9.09

tracheomalacia (GONE!! Sept08)
partial agenesis of the corpus callosum
residual VSDs post-surgery but lung pressures normal (Nov08),

?septo-optic dysplasia.


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Old 07-18-2009, 05:03 PM
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drct1245 drct1245 is offline
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It seems like no matter how hard you try and prepare... there is always something they don't tell you. I hope she is on the mend and not in much pain very soon...
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Dawn



former 26 weeker -- 4/2006 -- trach, g-tube, nissen; came home 1/07 vented 24/7; Successfully decanned 8/8/2008 -
Follow decan at: http://sleepy-dogs.blogspot.com/
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Old 07-18-2009, 05:11 PM
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JWorthington JWorthington is offline
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she is such a brave little girl. give her a huge hug from Sam xxx
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Sam Feb 11 2003 Opitz G/BBB syndrome, mickey, nissen, autistic,supraventricular tachycardia, bronchiolitis obliterans. decanned May 30 2009. 2 brothers Jonathan (23) James (14).
I am first and foremost a child
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Old 07-18-2009, 11:07 PM
TommysDad TommysDad is offline
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I'm glad to hear that it has gone very well. I have heard that some kids, even after having the stent removed, have decreased volume in voice due to swelling or some scarring. However, the parents were told it will get better with time, and it did. We'll be praying for excellent results when the stent is removed.

And don't feel bad about removing your daughter's NG tube. I can't tell you how many times we accidently did it or a nurse did it. It just happens some times. Your 7 days will be up before you know it, and you won't have to worry about it again.

Thanks so much for taking the time to update us. We all know how stressful recovery can be at times which makes us appreciate the update even more! Please continue to keep us posted as you have the time.

~Maggie
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Father (and mother) to Tommy, born via an emergency EXIT to Trache 8/1/06. Diagnosed with Congenital High Airway Obstruction Syndrome (CHAOS). VACTERRS Syndrome. Vocal cords completely fused until Double Staged LTP 03-03-08, refused shortly after stent was removed. Second Double Stage LTP 1-20-09.

CarePage: BabyBoyce

“With man this is impossible, but with God all things are possible.”
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Old 07-19-2009, 01:38 AM
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Thanks for the update! I guess it didn't occur to me that the stents would prevent vocalizing. Tommy wasn't ever able to vocalize until his stents came out. Hope the week goes by quickly for you.
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Rene, Mom to my Angel, Tommy. Born 9/25/06 at 33 weeks, with Single Ventricle Heart Defects and Cricopharyngeal Achalasia (Gtube dependant, poor swallow). Trached at 2 months for Severe Subglottic Stenosis. My little flirt died unexpectly 8/20/08 from complications from undiagnosed bronchopneumonia.


Forever, Tommy's Mommy http://www.musingsofaheartfamily.blogspot.com/
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Old 07-19-2009, 11:38 AM
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Ainsley's Mom Ainsley's Mom is offline
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I'm so glad to hear things went well. Don't you love those unexpected surprises?! I hope you're out of there soon. I can't wait to see Emily without her trach later this summer.
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SUSAN - Mom to Ainsley (age 6 - DOB 10/18/06) + Evie (age 12) and Adrian (age 9). Adorable and Trached since 11/06 (scarred vocal cords & OSA) but capping with mixed success since 1/09, sagittal craniosynostosis (cranial reconstructions 1/07 & 7/07), MicKey G-tube 06/07, Nissen 10/08, unusual form of cerebellar hypoplasia, hip dysplasia (Surgery 11/07 & 4/10), ptosis(post-surgery).

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Old 07-19-2009, 11:47 AM
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Kaylie Kaylie is offline
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what a remarkable little one you have . i am so thankful that things have gone good, i feel bad that she was in so much pain, but i hope they have that controlled now... keeping fingers crossed for all good things ahead..
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Old 07-19-2009, 01:08 PM
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I'm glad she's doing so well! That would be hard to deal with not being told about her vocalizations...I'm sorry. I hope you are out of there quickly.
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Old 07-20-2009, 02:42 PM
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day 4 and she is getting better but it seems slow. her doctor is surprised at how out of it she still seems. i am surprised because i expected her to bounce back more quickly. i am naive i suppose because i was thinking back to her heart surgery when she was a 6 month old and where she woke up through the morphine and was dancing around with a smile on her face. it was so different then though - she started out as a very sick baby and was "fixed" whereas this time she was a very healthy 2 year old subjected to a big op.

anyway...she is doing well and the next stage is approaching quickly.

all i need do now is keep my gob shut a bit and try not to fight with any more nurses.
__________________
*clare.
mum to emily
12/02/07 (placental abruption)
APGARS 0+1 (HIE gr.2/seizures) but she MADE IT! with the determination that we still see in her every day.
Grade III SGS - emergency tracheotomy July 2007.
2 stage LTR July 09 - DECANNED 27.9.09

tracheomalacia (GONE!! Sept08)
partial agenesis of the corpus callosum
residual VSDs post-surgery but lung pressures normal (Nov08),

?septo-optic dysplasia.


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  #10  
Old 07-20-2009, 02:48 PM
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KJKK8437 KJKK8437 is offline
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Quote:
Originally Posted by saywhatyouwill View Post

all i need do now is keep my gob shut a bit and try not to fight with any more nurses.
That was always my problem.
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Karin
Alex's Mom
Alex born 6/19/2007, PRS, Trached and GTube at 3 weeks, palate repaired 12/20/2007, failed decannulation 5/7/08 due to undiagnosed suprastomal collapse, jaw distraction 9/9/08 (insertion) to 10/30/08 (removal). Single Stage LTP 2/17/09 and now member of the Naked Neck Club. Need a laugh? Check out http://itsallgoodtoday.blogspot.com/

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