Added: 3 years ago
From: justCabz
Views: 4,182
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  • I also had a daughter born with gastroschisis in Feb '07.... She'll be turning 5 in just a couple weeks and is doing great!!! Spent 3months and 4 days in the NICU but luckily haven't had any problems since..... Bless you and your family ;-)

  • Simply WONDERFUL video. Made me cry.

    My niece's baby was just diagnosed with this condition today.

    We love you Izayah Michael!!!

  • Its graet to know that your little girl is healthy and I hope that she gets to live a long happy life! I know what its like to deal with gastroschisis... I was born with it and I am happy to say that I have lived a healthy 17 years! good luck on your journey

  • Your video almost made me cry.. very beautiful & im so glad she is doing fine and healthy!

    im due 3rd november 2010, we found out at my 19 week scan our baby girl has a Gastroschisis.

    your storey is beautiful. xx

  • @hollynsarahrhot I'm due on October 29th but about an hour ago i found out i will deliver by 37 weeks. My baby also has gastroschisis. Me and my boyfriend have been going through an emotional hell since finding this out. i haven't had anybody with this condition so i havent had anyone who understands what im going through. if you need someone to talk to you can email me at cee_cee_chikka@msn.com

  • you're very lucky... my baby girl died with gastrochisis she was 5 days old.. she was born january 1 2010 at 12:47am and died january 6 at 3:00pm.. a new year baby.. the operation was successful but she had this infection called sepsis..

  • touching video..thanks for sharing!

    my son was born oct 24th 2009 with gastrochisis

    i had him at 35 weeks praying for a fast recovery

  • Thank you for sharing your story. I am 26 and seven months pregnant. My baby boy will be born with the same defect. The doctors tell me he has a good chance. In our case our baby will be taken to Corpus Christi, Texas to a Driscol Hospital for children a couple hours away from where I live so it will be a long journey. I hope our story ends the same way yours did.

  • Thanks for sharing your story! My daughter McKenzie Reese was born on 12-6-07 with Gastrochisis. Your video brings back so many memories. I hope your little one will grow up to be as healthy as my little one has.  Truly a special video :-)

  • your video is beautiful, my little girl was also born with gastroschisis, we were in loma linda for 3 months she is now 1 year 7 months and is very healthy, everything is possible with prayer. god bless your family and kisses to your little one!

  • Thank you, and yes.. everything is possible with a prayer.. god bless you and your family as well :)

  • What a coincidence!! My son was born with gastroschisis on the same day as yours, July 25, 2008 at Montreal's Children's hospital...After 6 surgeries and a 3 month stay at the hospital, I was able to take my son home. You have a beautiful baby girl ! Love and prayers coming your way!

  • i was really touched by your video, im really emotional im 15 weeks pregnant and found out my baby has the same condition, thank you for the video it was really inspiring, good luck and god bless

  • No problem, if you ever need to talk or have any questions please let me know. God bless you and your family.

  • she was born september 3rd and was home just in time for her first holloween shes is now almost 3 years old and doing PERFECT

  • That's great to hear, I love how these Gastroschisis babies can be so strong even though they go through so much at such a very very young age. My daughters 8 months on the 25th of March and she's such a calm and happy baby, it's like nothing ever happened <3

  • my daughter was also born with gastrochisis she was born it 2006 i only got to see her for 15 mins after birth and then they took her to sick childrens hospital she had her first surgery at 2 hours old and many more from there we had many complications she kept pushing her intestines back out and pulling her breathing tubes out allt he time she was in the hosital for 2 months

  • Congrats on your baby shes gorgeous. My cousins baby was born with this condition but hers was forming very early and when she was born almost nothing could be saved. She lived in childrens hospital for 4yrs and passed away a week before her 5th bday. Not trying to hurt you but i wanted to share with you our experience and you are very lcuky..congrats

  • Thank you so much, and tell your cousins my prayers are with her, hope she's doing fine.

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