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We still have Corin and Tara and who else???? Penny, we'd love to see you there! Friday and Saturday morning... all about CHERUBS and medical stuff and learning and talking at the conference.... support group stuff. Saturday night is about CHERUBS too but it will be about all of us able to hang out and have fun as friends too!
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.
Now that things are a bit settled here I need to shop in earnest so hopefully when we get back from PA this weekend. Maybe I will find one there
Tara
Mom to Brandon 7/17/96 LCDH repaired six times- ECMO seven days- nissen and g-tube at three weeks- g-tube removed at five years- slight scoliosis Also Co-Rep for the State of Ohio
I bought my shoes for the ball last night and we picked out and ordered Chuck's tux. Went to MW Tuxedo (Men's Wearhouse). Went with a black tux with white shirt and Ivory vest and neck tie.
Kara- mom to Aaron (8-30-03) and Adam- LCDH (8-7-06). Gastric Volvulus at 7 months old; Borderline Chiari Malformation; reherniation- bowel blockage and intestional malrotation at 26 months old; Apraxia of Speech - neurological speech disorder; Auditory Processing Disorder; Asthma; and frequent headaches.
That's great Kara!!!!!
I found shoes--but Shane does not like them!!!! Who cares---I am going to go get them anyways.
That's good you have Chuck's tux on order.
When will you pick it up?
I better get Shane to go to the store in town and get his ordered.
Thanks for the reminder.
You and Chuck will match nicely!!!!!
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]
Ya'll I just cant do it !
I just cant dress , I know I'm awful !!!
Yes you can! Do it for Cole!
Kara- mom to Aaron (8-30-03) and Adam- LCDH (8-7-06). Gastric Volvulus at 7 months old; Borderline Chiari Malformation; reherniation- bowel blockage and intestional malrotation at 26 months old; Apraxia of Speech - neurological speech disorder; Auditory Processing Disorder; Asthma; and frequent headaches.
I'll let you wear flip flops under that dress, Penny : )
Kara- mom to Aaron (8-30-03) and Adam- LCDH (8-7-06). Gastric Volvulus at 7 months old; Borderline Chiari Malformation; reherniation- bowel blockage and intestional malrotation at 26 months old; Apraxia of Speech - neurological speech disorder; Auditory Processing Disorder; Asthma; and frequent headaches.
LOL thank you Kara !!!!!!!!!!!
I cant wait to meet you, you are a hoot !
I found a silver dress i like but once again with this blonde hair and fat @$$ i will run the risk of looking like a baked potato
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
That's a great analogy. I'll have to remember that one.
Penny, there ought to be an informal white gown out there that'll work for you.
Kara- mom to Aaron (8-30-03) and Adam- LCDH (8-7-06). Gastric Volvulus at 7 months old; Borderline Chiari Malformation; reherniation- bowel blockage and intestional malrotation at 26 months old; Apraxia of Speech - neurological speech disorder; Auditory Processing Disorder; Asthma; and frequent headaches.
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