Wednesday, August 11, 2010

Ciaran's Angels

There is a very special little boy who happens to share a birthday with Skeeber. His mother and I met in an online forum. We talked a bit before the boys were born, but have since grown closer. We can talk about our boys for hours and since they are the same age we can come to each other with concerns. One day we hope to get together so our little birthday buddies can finally meet.

There is one major difference between Mason and Ciaran though and that's the fact that Ciaran was diagnosed with CDH or Congenital Diaphragmatic Hernia.

Taken from the CDH website:

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.

Every baby with CDH is different - like a snowflake, no two are alike. What works for one baby, may not work for another. There is no reliable indicator to predict if a baby will do well or not. Babies with no diaphragm and little lung sometimes do well, while babies with 2 full lungs can sometimes do poorly. Head to lung ratio is used to determine whether to intervene prenatally through in utero treatments but it does not indicate a true survival rate. "Lung function" is also not an indicator as there are many other factors at work with these children such as kidney function, brain function, other birth defects, possible complications or infections while in the hospital, etc

In honor of Ciaran I have started the fundraising process to help with CDH research. Please take a moment to visit our site and educate yourself on CDH. There is also a place to make a donation if you wish. Every little bit helps. Please help us spread the word on CDH by sharing our facebook page with your friends.

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