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65 Reviews
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May 13, 2010

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May 13, 2010

My son was born with CDH. I heard about Breath of Hope from the social worker at UCSF. Breath of Hope has many families going through the same thing, and it's nice to know that you aren't alone. It's also great to be able to give advice to new parents who are just coming into this whirl wind of an experience and give them hope and encouragement. This organization also influenced me to go out and get Congenital Diaphragmatic Hernia Awareness day a proclaimed day of awareness in the city I live in.

The Great!

I've personally experienced the results of this organization in...

I joined this group when my son was diagnosed with Congenital Diaphragmatic Hernia.

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How frequently have you been involved with the organization?

About every week

When was your last experience with this nonprofit?

2010

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3 hours of volunteer time for this nonprofit will...

Edit our newsletter, create graphics, help families who have been affected by CDH, distribute our materials to hospitals or health care who may distribute it to families who could benefit. Help review or edit our materials.