#3
Stay Connected 
Stay Connected
Bracelet #1 - Screenprinted with clouds and pink, blue and yellow with "Congenital Diaphragmatic Hernia Awareness"
Bracelet #2 - White with screenprintedribbon logos and "Congenital Diaphragmatic Hernia Awareness"
Bracelet #3 - Black with screenprintedribbon logos and "Congenital Diaphragmatic Hernia Awareness"
Bracelet #4 - Standard rainbow with "CDH Awareness" and "www.cdhsupport.org"
Bracelet #5 - Standard rainbow with "Congenital Diaphragmatic Hernia Awareness"
Bracelet #6 - Standard pink and blue clouds with "Congenital Diaphragmatic Hernia Awareness" - we'd have to order 2 batches (1 blue, 1 pink)
Bracelet #7 - Standard pink and blue clouds with "CDH Awareness" and "www.cdhsupport.org" - we'd have to order 2 batches (1 blue, 1 pink)
#3
They all look great, Dawn. The black one seems a little "dark" for me. I like #1 and #4. The colors are cheery
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]
I have to agree with Kate that the black one seems a little "dark" for me too, almost depressing and sad.
Tracy - mom to Ian, LCDH diagnosed at birth, 4/3/04. Ian was born at 36 weeks, spent 53 1/2 days in NICU, 7 days on ECMO, surgery was on day 5, 29 days on a vent, 23 days was an oscillating vent, 546 days on oxygen. Inguinal right and left hernias and undescended left testicle surgeries were done on day 48. Currently has heart related medical issues and exercise induced asthma, but is one happy, happy boy!! Also mom to Cole - 13, Shane - 9, and Toby - 4. CHERUBS Parent Advisory Board Member and Co-Chair, Volunteer Co-Coordinator, and Wyoming State Representative.
email: tmeats@cherubs-cdh.org
# 3!!
#2 or 3
[B][align=center]Dad to CDH angel Logan James. He was born June 14, 2006 - but sent up to heaven 4.5 hours later. His mom and I were both only 17 when we found out we were going to be parents, and we were 18 when he was born. He was born just a few weeks after our last day of high school. I'll carry his memory with me forever, and when I have more kids they will always know about their big brother.
#3 for me
Angela - mum to Max (LCDH 30/4/05 - 21/5/05) Also mum to Joseph 9- Christopher 7 and Dominic 2.
#2 or #3
LCDH diagnosed at birth- surgery repair at 2 days old- vent 9 days- came home after 25 days in the NICU!
Three!
~Mel Mother of Michael: RCDH- ECMO (11 days)- cranial evacuation- VP shunt- hernia repair- g-tube- Nissen fundoplication- pyloroplasty- ASD and VSD closures- tracheostomy- hypospadias repair- pulmonary hypertension...but what he lacks in lung capacity he more than makes up with charisma!
#3
Posting Permissions
Reply With Quote