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