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  1. Hi I am a new member!

    Hi I am new. My son was born with a right diaphragmatic hernia in 1981. I have always wanted to talk to others about my son and all the problems that have followed him. Even today he is still having issues, medical and neurological. I am not sure this is getting out to anybody. But if it is please write back.

    longing to hear from others.

    CathyL
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  2. Concerned parent

    Hi I'm new to this but I have a 5 month old left side cdh he doing great but we have recently ran into some feeding issues . He has a g tube so we can feed him even when he want take his bottle thank goodness . He use to take his whole bottle no problem we only used tube at night for night feeding while he sleeps to help him grow but the past 3 weeks he has stopped taking them we are tubing all his bottles all the doctors will say is acid reflux but he doesn't act like that's what it is .... But ...
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  3. Anyone in New Zealand with CDH??

    Hi, I am 16 years of age with CDH, I am from New Zealand and would like to know if there is anyone else in NZ with this condition?
    Ella
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  4. Parent to a CDH survivor (new member)

    Hi everyone. I am a parent to a left congenital diaphragmatic hernia survivor. My son Marcus Anthony Velasquez is now 10. He only had a 20% chance of living but he beat all the odds. He was on ECMO for 13 days. It was the scariest time in my life. He stayed almost three months at the Driscoll Childrens Hospital in Corpus Christi, Tx.
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  5. Proud Member of CDH Angel Club!

    So excited to be apart of the club!
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