© 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
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.


































































































If you would like to donate specifically to help our Foundation fund this event,
please do so by noting that your donation is designated for the
Making Tracks Together Family Gathering.

Thank you so kindly for your contribution to help us better the lives
of those families affected by congenital CMV.































Click on the above link to download the fundraising documents...get
started today to
raise funds for your registration fees & guest room
costs
AND raise CMV awareness at the same time!
Making Tracks Together

    For many years, families affected by CMV have not had an outlet designed specifically for them.
    As such, we have organized this fun and informative gathering for families with children affected
    by CMV.

    The 4 day event includes expert guest speakers as well as parent speakers. There is plenty of
    formal and informal question & answer time throughout the entire event. As well, one entire
    day, "Fun-day Friday", is spent as a group in the water park with all of our families together!

    This is a fantastic opportunity for families affected by congenital CMV to build community, to
    share stories, advice, ideas, and undoubtedly some tears of both joy and sorrow. Our
    Foundation is honored to bring this special event each year to CMV-affected families across the
    world, providing the much needed support and unity within our special community of families.

                             Start making your plans now and we will see you all there!!
3rd Annual
Making Tracks Together
June 28 - July 1, 2012
Great Wolf Lodge
Kansas City

"It TRULY was an AMAZING experience. Each &
every single person there was awesome! Everyone
got along so well & were great with our special
lil' kiddos! A big THANKS to everyone there for
sharing their amazing families with us!"
- Jesica R.

"I just can't describe the
feeling of being there
families. It was truly
amazing. For the first
alone in our fight against
CMV. It was like we
had all known each
other for years.
We all just
kind of clicked"
-
Crystal T.
families going through the same things that we are
these great kids and parents. It helps you not to feel
so alone with the enormous task of taking care of our
precious kids. It was an unforgettable trip."
      -
Bonnie F.