Please Vote Today - This is your daily vote reminder to help babies born with Congenital Diaphragmatic Hernia!
CHERUBS is participating the Vivint Gives Back Contest on Facebook and we need your votes! How to vote:
1. Go to http://www.facebook.com/VivintHome and "Like" Vivint
2. Go to http://www.voteforcdh.org/ and click the Vote button
3. Log in through Facebook and Vote!
4. Repeat #2 and #3 daily through August 27, 2011
Contest Update - Only 5 weeks left in the contest! It's not too late to start voting daily. Every vote counts!
Contest Voter Tip Of The Day - Order free "Vote for CDH" t-shirts and other items at Vistaprint. Details posted on http://www.voteforcherubs.org/
More Contest Info - visit http://www.voteforcherubs.org/ for information on how you can win prizes in our voter raffle, the contest video, free graphics, learn where the money would go to help CDH babies and more.
Did You Know? - Congenital Diaphragmatic Hernia is a birth defect that affects each baby differently. Some babies have small holes in their diaphragms or no hole at all, just very loose muscle. Some babies have large holes or no diaphragm muscle at all. The organs that migrate into the baby's chest cavity varies. Some babies have just a little stomach above their diaphragm while overs can have stomach, liver, intestines and other organs migrated. The amount of organs in the chest cavity controls the impairement of lung growth.
Meet Our Cherubs! - This is Braden and his big sister Brooke. They are the worst of enemies and the best of friends. Braden was born with an undiagnosed congenital diaphragmatic hernia on March 13, 2008. Within an hour of his birth I was told he would require surgery. He was taken from me and flown to CHOP where he received great care. He had his repair surgery the day after his birth and was home twelve days later. Braden's journey continues today as he struggles with weight gain and asthma like symptoms. Please vote so that all mothers can have the benefit of knowing what they are facing before their child arrives. CDH babies need special attention at the precise moment of their birth!
- written by Braden's mom, Karla Holt
Thank you all for your support and your votes to help CDH babies!
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Vote for CHERUBS at http://www.voteforcdh.org
Contest Info, Fliers, Graphics, etc at http://www.voteforcherubs.org/
Facebook CDH Voting Group at https://www.facebook.com/home.
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CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support
Public 501(c)III non-profit organization serving over 3000 CDH families in 38 countries. Searching for the cause, prevention and best treatments of CDH since 1995.
http://www.cdhsupport.org/
http://www.cdhresearch.org/
http://cdhsupport.blogspot.com/
http://www.cdhconference.org/
Phone - 919-610-0129 E-mail - info@cdhsupport.org
Mailing Address - 3650 Rogers Rd #290, Wake Forest, NC 27587, USA
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