thread: Sophie's HIE journey

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  1. #1
    Registered User

    May 2006
    Igglepiggle Land
    2,742

    Sorry Claire - I always associate babies in NICU as being prem, (as my daughter was quite prem), sorry, force of habit .

    What I mean to say that it is totally inspiring to see kids born with difficulties, who go through such a hard time to get well in NICU type places, end up blossoming and beating the odds the medical profession sometimes give them. That extends to all kids / babies, not just the premmies.

  2. #2
    Registered User
    Add aussienic on Facebook

    Feb 2005
    Boyne Island
    6,327

    amazing (and gorgeous ) little girl... Thanks for sharing your Story

  3. #3
    Registered User

    May 2008
    Country VIC
    381

    Gosh Claire what an amazing little girl!
    Congratulations!

  4. #4
    Registered User

    Feb 2008
    Near the Snowies!
    2,975

    What an amazing story, congrats on your gorgeous little girl, she certainly has overcome a lot in her life so far!

  5. #5
    Registered User

    Oct 2007
    ★ nor here nor there ★
    4,134

    Welcome to BB, and WOW!!!

    You are an amazing mother for having complete faith in your daughter, I love it when babes defy the odds and proove the medics wrong

    She is just gorgeous, and she has come so very far, thank you so much for sharing your story

  6. #6
    Registered User

    Sep 2008
    Australia
    471

    Welcome to BB. Thanks for sharing your story with us. Truely inspirational.

  7. #7
    Registered User

    Jul 2005
    Sydney
    4,517

    Hi Claire,

    welcome and thank you for sharing your daughters journey. what a scary start for you all.
    I'm so happy to read how well she is doing now and defying what the medical professionals told you!

    My son was born @ 33 weeks but in his first 48hrs he had a seizure. The cause what thought to have been either a grade II hamhorhage in his left brain ventricle or HIE.
    we were told at that stage they did not know if he may have caused anything (they beleived it had not though and he never had another seizure) and it was a matterof time to see if he reached milsetones etc, which he did.
    He turns 4 in April, he is a beautiful boy, he is actually having a big assessment tomorrow (which goes for 4-5hrs) to diagnose if he has Autsim or PDD (Pervasive Developmental Disorder)
    he is speech delayed and has a sensory processing disorder but he is going to speech & OT at the moment and both are making a big difference in his life!
    I hope your daughter continues to proove her strength and fighting spirit!