Great photos thanks for sharing Steph
Stay Connected 
Stay Connected
Great photos thanks for sharing Steph
I had such a great time! I will have to post the few pictures I have tomorrow. I miss everyone already! There were definitely a lot of laughs and a lot of tears. I wish we could do it more often!
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
Great photos - so glad you all had the chance to catch up
Danielle- mum of Alyssa 21-22/05/92 L-CDH diagnosed at birth
I love the photos!!! Lots of smiles! It is great to see you all and also to see you all together!
xx
Jaana - mum to Gabriel and his big sister Shaddel Liisa. Diagnosed 19 weeks in utero with LCDH. Polyhydramnios. Surgery day 3 - collagen patch. 8 days vent and 3 days oxygen. 6 days NG Tube. Home after 13 days. Additional surgery at 7 weeks for bowel obstruction - reflux settled. VSD closed naturally and no problems with lungs. http://i316.photobucket.com/albums/m...abKiasmall.jpg
Fabulous pics! I'm so happy you girls could all get together! Love hearing about it - the next best thing since you are all TOO far away.
Lynne, Bayer is getting so big and cuter by the day!
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
Great pics! Looks like a lot of fun!
We did have such a great time! I am sure that Shane and Steve were going crazy with all the girls! LOL I LOVED it!! So so many girls!!
I still have to pull my pics from my camera but will get some posted soon!
Amy-love your blog.
Carrie's newest little one is beautiful.
I think we should do a CHERUBS get together every month in different states!! WOuldn't that be great???
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]
INFORMAL get-togethers between friends (like what you ladies had in Indiana)....
Otherwise I'll be getting an ulcer helping plan stuff every month!
Unless of course you can get the State Reps to plan those!
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.
That would be GREAT if the State Reps planned get-togethers! hint...hint....
We could have our choices on where to go!
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]
Posting Permissions
Reply With Quote
