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Christie L.

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Brendan B. McGinnis Congenital CMV Foundation
July 2, 2011

The Brendan B. McGinnis Congenital CMV Foundation is dedicated to the CMV Families, raising awareness and CMV Vaccine Research. We found this foundation on the web when my son was finally diagnosed with cCMV at almost 3 years old. They have connected us with so many families affected by CMV all over the world. Being in the military and having this foundation on our side always will mean that wherever we will be next, we can connect with other families near by and will never feel alone again in this struggle.

The Great!

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

getting connected and staying up to date on CMV research and legislation.

Ways to make it better...

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

none!

More feedback

How would you describe the help you got from this organization?

Life-changing

How likely are you to recommend this organization to a friend?

Definitely

How do you feel you were treated by this organization?

Very Well

How did you find this group?

Google

When was your last experience with this nonprofit?

2011

MY ROLE:
Client Served & I was connected with other families affected by cCMV.