


| 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) |
| 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... |
| Jayce was born full of love and laughter. He spent his life touching the hearts of anyone that saw him. He had eyelashes that would make the girls jealous and a smile that would melt even the strongest of hearts. From his cute little dimples to his cute little buns, no one could resist falling in love! Although Jayce's illness made him fragile, he possessed the strength, perseverance, and courage to overcome incredible odds and physical challenges. a memories. Jayce has shown us all how fragile and important life can be. He has taught us how to love unconditionally and the true meaning of love. He has touched more lives than can ever be imagined and has left his hand print on more hearts than can be counted. Thank you for showing us the way. You gave us meaning and filled our hearts more than we could have ever thought. Spread your wings and fly, our little Angel. We thank you for sharing your life with us and will forever be touched. We love you, Buddy." Submitted by his mom, Brittany |

