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This fundraiser ended on 02/01/12

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Hug your kids then help families win the battle against congenital diaphragmatic hernia (CDH). Show your support, Say "I Love Angel Strong!


CDH Family Assistance Fund – This fund will go to help families with their monthly expenses such as mortgage, electric and food. It will not go to any wants only needs. Families will submit confidential applications for assistance to Silas Foundation whom will consider each request.

Our goal is to make sure that all CDH families can afford to get to their cherub’s medical care and not have to worry about missing work due to their Cherubs medical battle so that they can concentrate on their children instead of money worries.

* $5 can buy the detergent to keep germs away.
* $10 can cover a family's gas for a day.
* $20 can feed a family of 4 dinner for the day.
* $50 can pay their phone bill to communicate with doctors.
* $200 can cover the monthly electric bill for a family.
* $500 can cover a families car payment.
* $1000 can help pay a families mortgage.

What is CDH?

Congenital Diaphragmatic Hernia (CDH) occurs in approximately 1 in every 2,500 births (1,600 cases in the U.S. each year). The cause of CDH is not yet known. The diaphragm is formed in the first trimester of pregnancy and controls the lungs' ability to inhale and exhale. CDH occurs when the diaphragm fails to form or to close totally and an opening allows abdominal organs into the chest cavity. This inhibits lung growth.

Every patient diagnosed with CDH is different. Survival rates depend on the types and number of organs involved in the herniation and the amount of lung tissue available. There are many surgical procedures and complications that may or may not occur with each individual, including in utero surgery.

Roughly 50% of babies born with CDH do not survive. Of the 50% that do survive, most will endure long hospital stays, feeding issues, asthma and other problems. A few of the survivors suffer from severe long-term medical issues.

CDH occurs as frequently as Spina Bifida and Cystic Fibrosis, yet there is very little research being done and virtually no media coverage.
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