Oh my goodness!! That's the first time I've looked at some of the YouTube videos. They are truly amazing. Kate you couldn't have done a better tribute for Shannon, I'm crying right now. I hope I can put one together soon for Lily.
Oh my goodness!! That's the first time I've looked at some of the YouTube videos. They are truly amazing. Kate you couldn't have done a better tribute for Shannon, I'm crying right now. I hope I can put one together soon for Lily.
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
I LOVE the video. Its so precious!!! I love to make those videos!! Here is Aydas video
http://youtube.com/watch?v=r-VPa4FABC4
I want to update it once I get more pictures to.
Hey, I am making this huge poster for my fundraiser and I am trying to get as many pictures of CHERUBS that I can. So far, I have 3 babies, but I would like to have more. If you would like, just email them to me.
shanellbrowand@live.com
Loves,
Shanell
Shanell Browand- CHERUBS Idaho State Representative, mommy to Ayda Rose Browand, our one and only (LCDH- 4 CDH surgeries, 2 surgeries to remove fluid from around her heart, has severe hearing loss, asthma, febrile seizures, weak immune system)
Shannell, I would love to send you some of Shannon's pictures, I don't have any saved on my laptop so as soon as I can get my lazy butt down stairs to the other computer I will get you some!!
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]
Yeah, there is no rush on the pictures. I am going to ask for pictures up until a week before my fundraiser. I am the same way with my laptop. I like mine only, but sometimes my husband likes to use it, but I am to lazy to go into the other room and use the desktop!
Shanell Browand- CHERUBS Idaho State Representative, mommy to Ayda Rose Browand, our one and only (LCDH- 4 CDH surgeries, 2 surgeries to remove fluid from around her heart, has severe hearing loss, asthma, febrile seizures, weak immune system)
I'll send some too Shanell. Ayda is so beautiful!
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
I finally went through Graham's ICU video and put something together....it was harder than I thought... I didn't realize how much video I'd taken...
here it is....
http://www.youtube.com/watch?v=Vle_oLYp2bc
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/
It was done perfect. I cried.
Thanks so much for sharing Cristin.
Ok, I have a question--which video would you like me to use for the video I am working on?
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 meant to add--Cristin--Graham is a miracle!!! I know you know this--but to go through ECMO twice----HE IS AMAZING!!!!!!!
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]
Cristin,
Graham's video is perfect!
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
Cristin,
I loved Graham's video, he is a gorgeous looking child. I really liked how you explained ECMO was great for me. I see a lot of you write about your babies being on ECMO and I did go in to the research section and saw it was a lung/heart bypass machine. But I didn't realise that it was a last resort as you put it in your video. So thanks, I'm constantly learning. He is a little fighter!!
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