Date Range
Date Range
Date Range
Sunday, November 28, 2010. All in all we are so pround and thankful to have our wee star Kaden x. Sunday, November 28, 2010.
CDH parents giving Information, Support and Hope to families expecting babies with Congenital Diaphragmatic Hernia. Tuesday, December 28, 2010. CDH HOPE Baby Shower in honor of Aaron Younce. Aaron and NC Representative Shirley Randleman, who took time out of her busy schedule to attend and learn about CDH! On October 16, 2010 a fundraising baby shower was held for our CDH HOPE Totebag Project. In honor of Congenital Diaphragmatic Hernia survivor, Aaron Younce! Must have .
Congenital Diaphragmatic Hernia Blogs Webring. This site is part of an Internet Site-Ring Community. Hosted at World of Newave.
Wednesday, July 6, 2011. Save the Cherubs Posters - Braden Holt. CDH survivor Braden Holt! A model for our Save the Cherubs. Congenital Diaphragmatic Hernia Awareness campaign! Photo by Ted Brooks. Posted by Dawn Torrence Ireland.
Older CDH Survivors FB Group. Grieving CDH Families FB Group. Founded in 1995 by 2 parents, CHERUBS is t.
Raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Sunday, January 28, 2018. Happy 25th Birthday, Shane. how can it be 25 years? I still feel 25 years old myself. Sunday, September 11, 2016.
How the Justice stole Christmas. How the grinch stole christmas.
Welcome to Florida CHERUBS! Wednesday, June 16, 2010. WELCOME ALL FLORIDA CDH CHERUBS, PARENTS, FAMILIES AND FRIENDS! I hope, through this blog, to create a community of Floridians who have been touched by CDH. Hopefully, we can share resources, ideas, support, and hope. To learn more about CHERUBS and CDH.
CHERUBS Illinois - Congenital Diaphragmatic Hernia. The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support. CHERUBS is the original CDH non-profit organization founded in 1995 to help families and medical care providers of children born with CDH. Monday, December 2, 2013. Is this Tuesday, December 3.
Congenital Diaphragmatic Hernia Blogs Webring. This site is part of an Internet Site-Ring Community. Hosted at World of Newave.
Our hope is that this blog will help other CDH families who just starting their journey. Monday, January 17, 2011. Long Over Due Jaxson Update. I wish you all a happy and healthy 2011! .
Kompetenzen lassen sich erwerben, aber nicht vermitteln. Deshalb gestalten wir Entwicklungsprogramme und Seminare so, dass sie den Erwerb von Kompetenzen ermöglichen und anstoßen. Wir achten dazu auf Praxisbezug und nutzen unser Knowhow aus jahrzehntelanger Erfahrung. Wie viele Häkchen setzt Ihr Team in der folgenden Checkliste.