YAY Kara! I am so excited!
I want sooooooooooooo bad to meet you all!
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YAY Kara! I am so excited!
I want sooooooooooooo bad to meet you all!
Fer Mom to Ana (29-11-2001) Mom to Juan Pablo (1-6-2007) born with a right sided diaphragm eventration- a rare type of CDH- severe reflux and speech delayed with signs of autism Juan Pablo- a Tribute to Life at http://es.youtube.com/watch?v=DYQAqMoTaiQ Our family blog at www.arcephoto.blogspot.com (if you want to visit- email me at maferarceamare@gmail.com so I can send you an invite)
Shauna, saying prayers that you can attend!!!
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.
Got my flight booked and booked a room for Corin and me today!WOOHOO! Is it July yet?!?
Danielle I am soooo excited to FINALLY get to meet you and Brenda after all these years!! Dang it now talk Shaz into comingtoo! LOL
I can't wait to meet you all.................. im very excited.
I'm so jealous!!
I've got tears thinking of our Danielle and Dawn meeting.
I'll need lots of pics of you all hugging Danielle.
Barb, you know I'd LOVE to come - we will have to settle with Skype.
xxxx
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
I will take many pics for you Shaz! and one day WE WILL meet!
I am all booked and ready to go!!!! Soooo excited! I can't wait to see all of you!
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
It would be fantastic if a few of the other aussie girls could go - but there will be other years so maybe we can almost always be representedI will be sure to share the whole event with them at our CAAF in Oct!
Barb, it will be soooo wonderful meeting all the 'old timers' and I was so excited when I heard Brenda was coming as well. I have also got to know so many of the'new timers' and can't wait to meet them. And if it is anything like the aussie gatherings, there are always people who have never really been as 'involved' who attend and you get to meet 'new' people. It is always the best!
Can't wait!!!!
Danielle- mum of Alyssa 21-22/05/92 L-CDH diagnosed at birth
I just booked my room, from the 21st until the 28th. They are getting pretty full she said, I was scared they wouldn't have a room for us!
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
ok now here is the big question.....WHO is all packed?!?! LOL
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