Brendan B. McGinnis Congenital CMV Foundation
Rating: 5 stars 14 14 reviews
PO Box 1719 Wheat Ridge CO 80034 USA
The Brendan B. McGinnis Congenital CMV Foundation is a non-profit 501 (c) (3) dedicated to raising public awareness about congenital CMV, to raise donations to support research for a vaccine for CMV, and to affect change in the medical community so that physicians will begin to test women for CMV prior to pregnancy. Ultimately, our mission is to save babies yet to be born from suffering the often devastating consequences of congenital CMV by eradicating this common but potentially life-altering virus.
In the past 6 years we have distributed nearly 27,000 informational pamphlets on CMV. We have held CMV Awareness Walk-n-Rollathons across the country for the past 5 years, raising awareness and donations to support our cause. We have professionally produced a PSA that is currently airing on national television in major cities across America. We present an annual award grant for Innovation in CMV Vaccine Research. We also have held a family gathering conference for the past 3 years for families affected by CMV across the country.
all women of child-bearing age, pregnant women, women considering pregnancy, the medical community, world wide.
Direct beneficiaries per year:
This is nearly impossible to determine as our awareness Campaigns are often online ads such as facebook, our website and you tube. Our annual vaccine research award recipient also directly benefited from our scholarship to help further CMV vaccine research efforts.
Geographic areas served:
all areas, particularly targeting women of child-bearing age.
Annual conference/gathering for CMV-affected families, called Making Tracks Together; annual grant award for CMV Vaccine Research; annual CMV Awareness Walk-n-Rollathons across the country, and PSAs which are airing on national television.
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Reviews for Brendan B. McGinnis Congenital CMV Foundation
It's a wonderful foundation dedicated to the CMV Families, CMV Awareness, and CMV Vaccine Research. We found this foundation via Facebook when my son was almost 2 years old and up until that point we felt so alone in our stuggles with CMV. They have connected us with lots of CMV families all over the world.
I've personally experienced the results of this organization in...
I've learned more about CMV and the affects of CMV through the Foundation than I did through any of the doctors or specialists that my son has seen.
If I had to make changes to this organization, I would...
I wouldn't change a thing. The foundation is wonderful!!!
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