© Copyright 2007 - 2011                       www.cmvfoundation.org                              Federal Tax ID #: 26-0886244
Public Awareness and Vaccine Research Support. Working Together to Eradicate Congenital CMV Disease.
Member of the External Partner Group, in conjunction with the National Center on Birth Defects and Developmental
Disabilities (NCBDDD) and the Centers for Disease Control and Prevention (CDC)
CMV Foundation YouTube Channel
The Brendan B. McGinnis Congenital CMV Foundation is a non-profit 501 (c) (3) dedicated to The
Brendan B. McGinnis Congenital CMV Foundation is a non-profit 501 (c) (3) dedicated to for CMV,
and to affect change in the medical community so that physicians will begin to test women raising
public awareness about congenital CMV, to raise donations to support research for a vaccine 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.

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In Loving Memory of...
Owynn
September 9, 2008 - November 19, 2009
Emily, Owie's mom, says of her son "He was beautiful in every way. He opened not only
me and my husband's eyes and those of his big sissy, but a lot of other people - many
who never got the honor of meeting him. He did more without ever walking or talking
than I will ever do. My little guy never let the pain get him down or show us he was in
pain. He always greeted us with smiles.

My daughter Devon says "Momma, remember my Owie's goofy smile?" He was
everybody's Owie! He had a way of making you feel like you are the most important
person in the world just by smiling at you."

Submitted by his mom, Emily