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CHERUBS - The Association of Congenital Diaphragmatic Hernia Research
April 4, 2013

2 of my 3 children were born with CDH, Cherubs has been a great place for me to find support, information and just talk with others who have been through what we have. They do amazing things to help educate people on CDH and families affected by it.

More feedback

Would you volunteer for this group again?

Definitely

For the time you spent, how much of an impact did you feel your work or activity had?

Life-changing

Did the organization use your time wisely?

Very Well

Would you recommend this group to a friend?

Definitely

When was your last experience with this nonprofit?

2013

MY ROLE:
Volunteer

CHERUBS - The Association of Congenital Diaphragmatic Hernia Research
April 30, 2011

10 yrs ago when the doctors told us our son Claude, would be born with CDH, we were clueless. We found CHERUBS and what a great place for support. 5 1/2 yrs later when Celie was born we found out she had CDH as well. I agian found strength and support with them. CHERUBS does so much for the families that are lost and dont know where to turn. I am thankful everyday I found this group and that it is here for other families as they go through this journey.

The Great!

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

The awareness and research they are helping to get for the CDH community

Ways to make it better...

If I had to make changes to this organization, I would...

Change their bank account so there was money to really get the campaigns out there. Most people have never even heard of CDH.

MY ROLE:
Volunteer & Meeting other families in my state with CDH babies.