Both it is then! You are not being a hog girl!!!!!!!
Both it is then! You are not being a hog girl!!!!!!!
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]
Thanks, Corin! I wanted to add it our Myspace so now I'll go do that. Thank you!
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.
I finally did Shane's video. I did great through his videos of him laughing and playing, the funeral photos killed me though. Up til 4:00 am this morning a blubbering mess. I made the stupid, stupid, stupid mistake of thinking I could handle the photos if I crossed my eyes really, really hard so it was all blurry when I looked at them at really fast and then I wouldn't see him, just the outlines of the photos. It worked... yeah, ok, sounds ridiculous and funny, but it did work. I didn't see details on any of the photo, thank goodness, but even without the details of him laying the casket... and I don't remember the hospital taking photos of the 3 of us after Shane died but apparently they did and I caught a glimpse of our faces and Jeremy crying... just killed me. I don't want to remember Shane like that, I've tried for almost 9 years to forget the funeral and his death... of course I can't, but I keep trying! I found a photo of Shane where you can only see the top of his baseball cap... that's included in the video. That's it, everything else is about his life. I forgot how silly he was.
The song choice is a bit odd, the first verse sounds horrible actually if you listen to the lyrics but the rest of the song is spot on, especially the chorus. It's a bit dramatic, but the purpose of the video is raise awareness and catch people's attention.
I felt like Shane was missing out without me doing a video of him... finally it's done. I feel like I got to spend some time with him last night, but it was still hard. But so worth it if it helps educate people about CDH.
Ok, enough rambling, here it is...
http://www.youtube.com/watch?v=8t22XUiNiaw
And another video I did last night - Taking A Stand Against CDH - about all of our and our support of each other.
http://www.youtube.com/watch?v=JtOElZcUyVM
PS - I think I may have figured out the e-mail issue, cross your fingers please!
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.
*Someone*... I have my ideas on who.... reported Shane's video to Facebook and had it removed because of the background song.
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- It is BEAUTIFUL!!!!! I am in tears, he looks so happy in all those videos! I am so glad you put that together! The song was perfect!
I'm sorry someone felt the need to take it off facebook-thats sad.
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
Beautiful video Dawn, you must be so pleased that you have finally made it. I don't know about you but making Jacob's video helped me so much
[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 I absolutely loved the video well done. It's a fitting tribute to a very special boy, he's so gorgeous!
Is it the second part that was removed, is that why it says it's 8 minutes but stops after 4 or so mins. I too think it's sad that someone did this to you.
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
Amazing, brillant, beautiful.
Thank you so much for sharing Shane with us.
I cried the whole time--but to see Shane smiling and to show all of these pictures of his life--can't even be described in words.
You did a fantastic job and whoever requested to have it removed from facebook--that is truly SAD.
The song is a great choice.
God only continue to Bless you Dawn--you have helped so many through CHERUBS.
Shane's legacy will live on forever through you and CHERUBS.
Shane smiles down at his Mommy daily and is so very proud of you.
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]
I made a video! Not of Alyssa. I want to try and get that done for her 16 birthday (later this month). I did one featuring all of our CHERUBS Australia Annual Forum photos. I have uploaded it to YouTube (amazed I managed all of this without a clue, lol) and now I don't know what to do. Dawn, do you add it to the other cherubs video's? The link is:
http://www.youtube.com/watch?v=keOCsSK48Z0
Please let me know if I need to do anything else. I am going to add it to the new aussie cherubs site I have been working on (for years I think!) and add it to my Facebook page.
Hope you enjoy it and can see how much we all love our annual gatherings
Danielle- mum of Alyssa 21-22/05/92 L-CDH diagnosed at birth
I know I've already said, but just wanted to say again what a great job you have done!!! Good on you Danielle
Dawn-here is the link for Lily's video as well, last time I checked it wasn't on the CHERUBS youtube site but I think I posted it in the wrong forum.
http://www.youtube.com/watch?v=6J6hN22f1ck
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