Hi Shaz
Those photo's are great!
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Stay Connected
Hi Shaz
Those photo's are great!
Maryanne (mum to Rebecca born 11/11/02 with LCDH)
Love the photos guys. Looks like you all had a great time. Can't wait to join you in Melbourne next year.
Here are some more photos
Lily
Rebecca
Ethan
Nicholas (Rebecca's brother)
Maryanne (mum to Rebecca born 11/11/02 with LCDH)
Oops. they're a bit bigger than I thought!
Maryanne (mum to Rebecca born 11/11/02 with LCDH)
Here is Liam, Nicholas and Chelsea-Rose at the zoo for our family day on the Sunday
Maryanne (mum to Rebecca born 11/11/02 with LCDH)
I love all the pictures you all have posted!! It looks like you had a great time, even the kids!! One of these days, I will get to meet you wonderful women in person!!! Look forward to hearing some stories and more of what happened.
Tracy - mom to Ian, LCDH diagnosed at birth, 4/3/04. Ian was born at 36 weeks, spent 53 1/2 days in NICU, 7 days on ECMO, surgery was on day 5, 29 days on a vent, 23 days was an oscillating vent, 546 days on oxygen. Inguinal right and left hernias and undescended left testicle surgeries were done on day 48. Currently has heart related medical issues and exercise induced asthma, but is one happy, happy boy!! Also mom to Cole - 13, Shane - 9, and Toby - 4. CHERUBS Parent Advisory Board Member and Co-Chair, Volunteer Co-Coordinator, and Wyoming State Representative.
email: tmeats@cherubs-cdh.org
Love the pics!!! Looks like you all are having a great time! I'm sooo jealous
Corin New England State Rep [img]http://i171.photobucket.com/albums/u312/GabrielMommy1118/1-3.jpg[/img] [url]www.gabriel-nava.virtual-memorials.com[/url] Gabriels website [url]http://www.youtube.com/watch?v=N66S-vt5sI8[/url] Gabriels Video [url]http://corinscrazylife.blogspot.com/[/url] My Blog [url]http://newenglandcherubs.wordpress.com[/url] New England Blog
Hi guys,
Thanks for posting all the photos, glad to hear you had a great time. Looks like you had a lot of fun too. Well done for organising such a great event. Can't wait for next year's to roll around! PS where are the hubbies? Did any of them attend?
xx Margaret
Hi Margaret,
The pic taken of us girls was a "girls dinner" we decided to have on Sunday night.
Our hubbies did attend the CAAF Saturday and dinner afterwards.
Damon loved the fact that everyone "got" what we all felt - our stories were all different (grieving and surviving) but we all had a common bond - CDH.
We hope to meet you next year.
love
Shaz x
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
GREAT PICTURES!!!!!!!
Looks like you had SUCH a great time!!!!!!!
You ladies are BEAUTIFUL!!!
The kids are all so CUTE!!!!
Looking at these pictures makes me SMILE BIG TIME!!!!!!
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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