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Thread: CAAF 2008

  1. #11
    You guys are going to have soooo much fun!! Take lotsa pics to share with us!!

    Barb

  2. #12
    You all have to post all the details like we did with the US conference and Angel Ball, etc - that way we can feel like we're there too! And lots of photos!!!
    Mom of Shane (1/28/93-9/11/99) LCDH x6 and multiple complications and birth defects.

    Founder and President of CDH International.

    Executive Director of:

    CDH International USA
    CDH International UK
    CDH International Canada
    CDH International Switzerland
    CDH International Netherlands
    CDH International Singapore
    CDH International Hong Kong

    Messages may be answered by CDHi Team.

  3. #13
    That's a done deal!!!!
    Danielle - Lily's mum. Lily 31.07.07- Diagnosed at Birth - LCDH- Repair: 13 hours old- Ventilator: 5 days- NG tube: 7 days- Hospital: 16 days. Also mum to Ethan 21/06/05 http://i256.photobucket.com/albums/h...nLilysmall.jpg

  4. #14
    Senior Member
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    Dani, I am also starting to get really excited. When I order my CAAF T Shirt was when it really started. Tanya (my dear friend from high school who also happens to be my SIL who is coming with me) and I are starting to decide what tourist things we will do. I am also really forward to our girls night - but NO singing from me. I will just have to laugh at Shaz and Dani
    Danielle- mum of Alyssa 21-22/05/92 L-CDH diagnosed at birth

  5. #15
    We won't complain hey Shaz!!! Danielle you sound like my husband - he WILL NOT sing ever!

    Danielle - It's so funny that Tanya became your SIL! My older brother and Brenton were mates so that's how we met, although they didn't actually go to school together.
    Danielle - Lily's mum. Lily 31.07.07- Diagnosed at Birth - LCDH- Repair: 13 hours old- Ventilator: 5 days- NG tube: 7 days- Hospital: 16 days. Also mum to Ethan 21/06/05 http://i256.photobucket.com/albums/h...nLilysmall.jpg

  6. #16
    LOl - Dani and I won't want to share the mike...
    Damon likes a sing too - He is better than me but sssshhh don't tell him.
    Sharon - mum to Liam - 30/04/03 RCDH- 2 CDH repairs- Vent: 22 days- oxygen: 315 days- ectopic right kidney- NG Tube: 3 years & 7 months Chelsea-Rose - 08/03/99 Co-Rep for Australia - sknott@cherubs-cdh.org http://i281.photobucket.com/albums/k...nLiamsmall.jpg

  7. #17
    You read my mind Shaz - I'm a 'hogger of the mike' too!!!!
    Danielle - Lily's mum. Lily 31.07.07- Diagnosed at Birth - LCDH- Repair: 13 hours old- Ventilator: 5 days- NG tube: 7 days- Hospital: 16 days. Also mum to Ethan 21/06/05 http://i256.photobucket.com/albums/h...nLilysmall.jpg

  8. #18
    5 sleeps to our PERTH CHERUBS Australia Annual Forum....
    Sharon - mum to Liam - 30/04/03 RCDH- 2 CDH repairs- Vent: 22 days- oxygen: 315 days- ectopic right kidney- NG Tube: 3 years & 7 months Chelsea-Rose - 08/03/99 Co-Rep for Australia - sknott@cherubs-cdh.org http://i281.photobucket.com/albums/k...nLiamsmall.jpg

  9. #19
    You all are going to have a WONDERFUL time!!!
    I am SOOOOOOOOOOOOOOOOOOO excited for all of you!!!
    ENJOY and take lots of pictures!
    Looking forward to hearing ALL about the wonderful time you will have.
    Stephanie (Shelby's Mom LCDH 7-10-06)- ECMO 7 days- 2 DH repairs- hital hernia repair- Cliff Lip repair- Nissen and Mickey button. Shelby is eating and drinking by mouth now!!! THIS IS FANTASTIC!!!!! Mom to Lexi 8- Morgan 6 and Taylor 5. Blessed to have our little butterfly and our beautiful girls. [url]www.youtube.com/cdhsupport[/url] - Shelby's Journey [img]http://i258.photobucket.com/albums/hh257/gracebutterfly/CDHAwarenessRibbonShelbysmall.jpg[/img]

  10. #20
    Hi Everyone

    Sounds like you guys are going to have a really great time in Perth!! Wish I was coming. I will definitly have to make it to Melbourne next year.
    Have fun.... and try not to get up to too much mischief

    xx
    Ang
    Angela - mum to Max (LCDH 30/4/05 - 21/5/05) Also mum to Joseph 9- Christopher 7 and Dominic 2.

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