Friday, March 4, 2011

2011 Congenital Diaphragmatic Hernia Cherubs Video

2011 Congenital Diaphragmatic Hernia Awareness Cherubs


900 photos of children and adults born with Congenital Diaphragmatic Hernia (CDH), a birth defect that affects over 1600 babies every year in the United States. CDH occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth. 50% of babies born with CDH do not survive. The cause is not known.

"Cherub" by Matt Panetta, in honor of his brother, cherub Jonathan Panetta.

"I'll Never Let You Go" by The Jammies. Written by Chad Knudsen in honor of his son, a CDH survivor.

For more information, you can visit CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support at http://www.cdhsupport.org/

Write your Congressman in favor of the CDH Research Bill - http://www.cdhbills.org/

Participate in "Congenital Diaphragmatic Hernia Awareness Daily" / CDH Prevention Day on April 19 by raising awareness and / or research funds.

2011 Save the Cherubs Video



Save the Cherubs
Congenital Diaphragmatic Hernia Awareness Campaign



http://www.savethecherubs.org/

Cherubs are everywhere. They are your next door neighbor's new baby. The little girl on the swingset at the park. The teenager that sits behind your son in high school geometry class. The person behind you in the grocery store line. Their scars are hidden under clothes, their stories a bit sad and taboo to talk about - so the miracles are not seen with the naked eye and you have probably mistaken a cherub for a "normal" person many times. But they are there; walking miracles with invisible wings. And missing babies that belong to the grieving parents who you don't see grieve; your local bank teller, the man who held a door for you at the gas station, the old woman who drove the car in front of you at the stop light this morning. Cherubs are everywhere.

Unless you have been affected personally by CDH, you probably have never heard of it. The mission of "Save the Cherubs" is to make Congenital Diaphragmatic Hernia a phrase everyone knows how to say and everyone knows what it means. By raising awareness, we hope to raise research funds to save these babies - Save the Cherubs.

Congenital Diaphragmatic Hernia occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth. Babies born with CDH often endure long hospitalizations and other complications such as pulmonary hypertension, infections, feeding issues, asthma and temporary developmental delay. Some babies develop worse complications and sadly, 50% of babies born with CDH do not survive. The cause of CDH is not known.

Cherubs are people who were born with Congenital Diaphragmatic Hernia, a severe and often fatal birth defect that occurs as often as Cystic Fibrosis and Spina Bifida. Every 10 minutes a baby is born with CDH - adding up to over half a million babies since 2000. Yet, CDH is given very little media attention, virtually no research money and until CHERUBS came along in 1995 there was no information and no support for families of babies diagnosed with CDH. We have no national telethons, no large corporate sponsorships. We have been struggling for years to bring attention to CDH and now, we are going to do so on a national level.

For 16 years, cherubs have been the awareness symbol of Congenital Diaphragmatic Hernia (CDH). Through this project, families around the world are working with CHERUBS, photographers and the media to raise CDH awareness in a unique and striking photo and marketing campaign, which we hope will take your breath away and make you want to learn more about CDH and how you can help save these children.

CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support was founded in 1995 to give hope and information to families of children affected by Congenital Diaphragmatic Hernia (CDH). We are a 501(c)III non-profit global CDH organization with members in 38 countries. CHERUBS strives to allow families to have free access to information materials, support services, awareness projects and to make a CDH connection with other families going through the same ordeal. We are just a grassroots organization of families working hard to make a difference and trying to give Congenital Diaphragmatic Hernia Awareness wings to take flight.
CHERUBS is fighting hard to search for the cause, prevention and best treatments of CDH. We invite you to help us to help these families and to help Save The Cherubs.
http://www.savethecherubs.org/

Thursday, March 3, 2011

Join The Angel Club!



Our new fundraising campaign gives everyone the opportunity to be a part of an elite group - angels helping babies who are fighting Congenital Diaphragmatic Hernia!



How do you join?  Just donate at least $1.00 to CHERUBS every month through our new Automatted Donation system through PayPal.   We know times are tough but every dollar helps and this is a great opportunity to help these babies by donating mere pennies each month without having to remember to send in a donation every 30 days.

About this campaign:
  • Donate as little as $1.00 per month
  • If you want to donate more, please do so!  You can set up monthly donations in any amount.
  • It's completely automated, you just sign up once!
  • It's through PayPal, the internets safest on-line payment software.
  • Donate through your own PayPal account or your credit card.
  • Unsubscribe payments at any time.
  • Donate in honor of in memory of your cherub!
  • Donations go to the CDH Support Fund



Join the Angel Club!
Enter the amount you want to donate each month
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Every dollar helps babies affected by CDH!
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