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Thread: bracelet

  1. 01-04-2009, 02:28 PM #1
    PennyCampsey
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    bracelet

    I want some ... where are ya steph ? ?LOL
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  2. 01-04-2009, 02:43 PM #2
    KimberlySwitzer
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    I got mine the other day.. I love them They are huge on me, I think im gonna keep them all for myself so I have spares!
    Mommy to Haylee 01/26/2004 and My cherub Asher 07/04/2007- LCDH discovered at 18 weeks- medical termination at 24 weeks. Hypoplastic left lung and right jaw- pulmonary hypertension- Secundum type ASD- left liver lobe- stomach- appendix- and small bowel herniated www.freewebs.com/babyasher Ashers webpage http://www.youtube.com/watch?v=dxS8F4dkHjE Ashers video montage
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  3. 01-04-2009, 10:43 PM #3
    StephanieOlivarez
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    How many you want Penny??? Let me know and I will get them sent out to you girl.
    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]
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  4. 01-05-2009, 11:18 AM #4
    PennyCampsey
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    I'll take 5 please :0)
    Do you still have my address ?? i can send you $$ whenever !
    cant wait !
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  5. 01-06-2009, 11:49 PM #5
    StephanieOlivarez
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    Sending you five Penny. I hope you LOVE them. I LOVE mine!!!!!!
    Stephanie (Shelby's Mom LCDH 7-10-06)- ECMO 7 days- 2 DH repairs- hital hernia repair- Cliff Lip repair- Nissen and Mickey button. Shelby is eating and drinking by mouth now!!! THIS IS FANTASTIC!!!!! Mom to Lexi 8- Morgan 6 and Taylor 5. Blessed to have our little butterfly and our beautiful girls. [url]www.youtube.com/cdhsupport[/url] - Shelby's Journey [img]http://i258.photobucket.com/albums/hh257/gracebutterfly/CDHAwarenessRibbonShelbysmall.jpg[/img]
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  6. 01-07-2009, 10:17 AM #6
    PennyCampsey
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    thank you STEPH ! will mail you $$$ just let me know the total ... !
    i WILL LOVE EM !
    i bet the kids at school will want one b/c MRS CAMPSEY has one!
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  7. 01-07-2009, 10:17 AM #7
    PennyCampsey
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    oh and the middle school age kids are all into cole and CDH
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  8. 01-07-2009, 10:20 AM #8
    PennyCampsey
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    ps .. a lady heard me talking about COLE's CDH last night while i was working at CVS , she was a customer. her son was born without and esophogus and trache ... they had to remove his lung to make one ! he is 12 now and was only supposed to live 1 year.
    AMAZING!
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  9. 01-07-2009, 03:13 PM #9
    LynneB
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    I need to order some braclets too Steph!
    cdh found at birth. 28 days NICU. Vent 7 days. Repair at 3 days. No ECMO. NG Tube 28 days http://i319.photobucket.com/albums/m...don/0004-1.jpg
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  10. 01-07-2009, 03:38 PM #10
    Dawn Torrence Ireland
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    WOW, that is amazing about that little boy, Penny!!! What a miracle that is he survived long enough to have surgery and now is doing so great!!!
    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.
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