Congenital Diaphragmatic Hernia Research Fund
Page Creator: Dawn Williamson
Page Closes: Sep 2, 2010
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www.cdhresearch.org
About my nonprofit:
CHERUBS THE ASSOC OF CONGENITAL DIAPHRAGMATIC HERNIA RESEARCH
CDH is a devastating birth defect, affecting 1 in every 2500 babies. It occurs when the diaphragm fails to fully form, allowing the abdominal organs to enter the chest cavity and prevent lung growth. CDH...
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Fundraising target: $10,000
Total raised so far: $4,555.00
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CDH Research Fund – to pay for the $1000 a year cost of  research database hosting and to raise money for research organizations such as the International CDH Study Group – unless a request is made to go a specific hospital.  The CDH Study Group is a collective group of over 30 hospitals around the world specializing in CDH research.  We chose to support groups like this one because we know that every cent will go directly to research on Congenital Diaphragmatic Hernia and research will be brooder and more advanced when collaborating with dozens of hospitals and researchers together. 

CDH Research Site - funds for the software needed to create and maintain secure database hosting for our CDH research database.  This database includes information on over 2400 CDH patients and medical care providers - offering  a very unique opportunity to research the cause, prevention and best medical treatments for Congenital Diaphragmatic  Hernia.   Such software and off-site security that is needed for an undertaking this large costs approximately $1000 per year (thanks to a grant from QuestionPro).  Rather than take funds out of our very small operating cost budget, we are appealing to members and the public to help fund this research venture.   Site maintence, design and statistics is being done for free by volunteers.  $1000 per year is needed solely for the database design and secure hosting, which is needed to follow federal privacy and HIPPA laws.

 

www.cdhresearch.org

 

This web site is a project of CHERUBS - The Association of Congenital DIaphragmatic Hernia Research, Awareness and Support.   It is supported by volunteers and funding through CHERUBS, a 501(c)III Non-Profit Organization.   Donations and sponsorships are greatly encouraged and appreciated to help keep this CDH Reseach site continuing, growing and leading the search for the cause and prevention of CDH.

CHERUBS Congenital Diaphragmatic Hernia Research Survey is the combined efforts of over 2000 CDH families and medical professionals.   It takes information on the medical, family and exposure histories of CDH patients and compares data to look for the cause, prevention and better treatement of Congenital Diaphragmatic Hernia.  Participation is voluntary, anonymous and free to all CDH families and medical staff.   Data can be tabulated live for research and reference purposes. 

Congenital Diaphragmatic Hernia (CDH) is a birth defect that occurs when the diaphragm does not fully form, allowing organs to enter the chest cavity preventing lung growth. CDH strikes 1 in every 2500 babies, of all races, religious backgrounds, and financial status - no matter how well the prenatal care.

Nearly 4 million babies are born in the United States each year.  This means that approximately 1600 babies are born with CDH each year - in the U.S. alone!    There are more babies born with CDH than with Cystic Fibrosis (1 in 3900) and it's almost as common as Spina Bifida (7 in 10,000)  - yet, you probably have never heard of it until it affected someone that you love.   CHERUBS is working hard to raise Congenital Diaphragmatic Hernia Awareness!

The cause of Congenital Diaphragmatic Hernia is not yet known.

50% of babies born with CDH do not survive and sometimes the remaining 50% have to overcome very difficult medical complications. Many CDH babies have minor lasting health problems such as feeding aversions, asthma, scoliosis, or short-term oxygen dependency.  A small number have major lasting health problems such as ventilator dependency, brain damage, or hearing problems.  Many patients have no long-lasting medical problems at all other than a scar from the CDH repair.  CDH can occur alone or with other birth defects, and rarely, it occurs as part of a syndrome.

Looking for support dealing with Congenital Diaphragmatic Hernia?   Make sure to visit CHERUBS - The Association of Congenital DIaphragmatic Hernia Research, Awareness and Support

Like the CDH logo or want to purchase some CDH Awareness items?  Make sure to visit CHERUBS Store where you can buy 100's of items with the Official Congenital Diaphragmatic Hernia Awareness Ribbon, the CDH logo, the CDH Anatomy shirt and much more. 

 


Online Donors to date:
Display Name Date  Comment
The Lynn Family 8/13/2009 In loving tribute to the little one who couldn't be with us 
Shandi Cox 2/19/2009 Thanks to everyone who donated money for Caleb's Valentine"s Day Fund Raiser at the Citgo in AL. 
Alyssa Hagen 2/1/2009 In loving memory of my angel McKenna, Shane,and all our other CDH angel in both heaven and on earth! 
Josh & Paige Cox 1/28/2009 Happy 16th birthday Shane! Please look after our little angel Caleb! 
Craig & Dawn Williamson 1/27/2009 Happy 16th Birthday to our son, Shane Torrence. We love and miss you, Shane! 
Elissa and Jason 1/22/2009 In memory of Jack Payne 
Robin and Klaus Keller 1/21/2009 In loving memory of our daughter, Kyra Maxime Keller. 
Paige Cox 1/10/2009 Caleb, you left us 2 months ago today.... We love you and miss you sooo much! ~Aunt Paige 
Leigh Creekbaum, mom to Grayton 12/29/2008 In Memory of Grayton Creekbaum, RCDH 5/09/08 - 6/22/08 
Nikki Haye 12/21/2008 For my beautiful daughter Soraya. 
Sharronda and Doyce Waldrop 12/18/2008 In memory of our little superman, Caleb Ray Cox 11-08-2008 - 11/10/2008. We love you! Nana & Poppa 
Shandi & Chris Cox 12/18/2008 For our baby boy Caleb Ray Cox. Born:Nov. 08, 2008 Angel date:Nov. 10, 2008 Mommy & Daddy love you!  
Darlene Silverman 12/17/2008 In memory of a brave little trooper, Shane Torrence. 
Paige Cox 12/17/2008 In memory of my nephew Caleb Cox 11/8/2008-11/10/2008. We love you Superman! 
Barbara M. 12/17/2008 In honor of John Murphy, an angel on earth! 
Anonymous 11/8/2008 11 years since we lost our son and still no known cause...help us find out why! 
PayneFamily 10/31/2008 For my son Jack and all CDH families 
Karla Holt 10/8/2008 for the miracle of my son Braden 
Barbara 9/6/2008 In Honor of Logan Lee Wagner 
Dawn Torrence 9/4/2008 In memory of my hero, my son, Shane Torrence (1/28/93-9/11/99) 
Shane & Stephanie Olivarez 9/3/2008 In Honor of Shelby Grace Olivarez- Daddy and Mommy Love you ALWAYS. 
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* Total raised online: $1,695.00
Amount raised offline: $2,860.00
Grand Total: $4,555.00
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