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This video is about families standing together against Congenital Diaphragmatic Hernia (CDH). It's about all of us, standing together, holding each other up.
Please forward, post on your profile and send to family and friends to help raise awareness.
Many of you may recognize yourselves here!
http://www.youtube.com/watch?v=3jvrB7CAnVY
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.
Dawn, i am glad you have done one using those photos as most of those ones i have removed from the montage that i made.
Well done on the video
Easy aren't they?
[url=http://counters.families.com][img]http://tac.families.com/cb/205944.png[/img][/url] [URL=http://img529.imageshack.us/my.php?image=cdhawarenessribbonjacobpf0.jpg][img]http://img529.imageshack.us/img529/1527/cdhawarenessribbonjacobpf0.th.jpg[/img][/URL] [url]http://jacob-ogilvie.memory-of.com/[/url]
Dawn that is a great video! I love the Rascall Flats Song, it is very fitting!!
Mommy to Shannon Elizabeth (01/16/07-01/19/07 LCDH and HLHS) Peanut Shelbe (miscarried 9/23/07 @ 8 weeks- due 4/10/08 ) Gracie Kathleen & Lily Anne (8/28/08 Blessings from their big sisters!) Shannon's Website! [url]www.shannonelizabeth.virtual-memorials.com[/url]
Great video dawn..and can i just say that the video u made of your son shane was really nice,and it made me cry,He would be very proud of the work your doing for us all...x
This is a great video!!
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
FANTASTIC video Dawn!!!
You did such a great job and the video of Shane...well I have posted on this and it is truly such an amazing video.
Shane will live on forever.
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]
Dawn,
I saw the videos a few hours ago and did a long post about it somewhere else where the video is mentioned. I'm lost on here! LOL
Great job and my hat goes off to you once again! I will definitely send it to everyone in my email addy lists on both my userids, to include former members of CHERUBS from years back that disappeared that I found their email addys again and can see them when they are logged on AOL.
Will be getting my loose pictures that had other get-togethers out of storage this weekend and also go through my Disney book and see if there are any others. If I find any that you can use, I'll mail them to you. Sorry, don't have a scanner set up in the trailer. o
xxoo Moi
{o/} ? /_?? Judi- Mommy to Jennifer Melissa- m/c 2-80 and Christopher Michael- 2-2-1989- left side CDH- born in Heerland- Holland- 1 repair w/dura- lived 19 hours. Buried in Milford- Connecticut. MD- VA- DC & CT State Representative. Mommy's and Mama's Guardian Angel and Inspiration! (Still trying to figure out the coding to put Christopher's Ribbon here also BUT IT'S NOT WORKING! SIGH & URGH!)
Great video Dawn - shows what a great group we are - so many gatherings over the years!
I also watched Shane's. We a wonderful way to honour your son and help raise awareness. It was beautiful to see the vidoes because I never got to meet Shane. I am so emotional though - I wish so badly I give your little boy back to you. Thanks for sharing him with the world!
Danielle- mum of Alyssa 21-22/05/92 L-CDH diagnosed at birth
The videos are great.... It must have been hard making Shane's video....I'm so glad that I got to know him a little better... Thank You...
Cristin Mama to Graham- RCDH diagnosed at birth. ECMO x2 19 days total- left nephrectomy- two brain bleeds- developmental delays- profound hearing loss- still tube fed but learning to eat!! Mama to Dottie born 02/23/07 big fat healthy baby who LOVES her brother!! www.caringbridge.org/ma/grahamrussell http://cdhmomma.blogspot.com/
The videos came out great! Thanks for putting them together! I was surprised to see us in it
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
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