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You might use this space to share more
information about your group's focus and why it
attracted your members, or to outline your
day-to-day activity. How often and where do you
meet? How do you stay current on developments
related to your interests? What plans do you have
for the future?

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Here you can tell your site visitors about your
successes as an organization. Have you contributed
to local, state, or national community events? Have
your members earned accolades or represented your
group at recent conferences? You might also
discuss notable trips, meetings, or other
developments here.

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You can use this space to
briefly describe a recent
event or group meeting.

We know first hand what it is like to be faced with hearing the diagnosis
of congenital CMV and the vast range of emotions that accompany that diagnosis.
Where can you go? With whom can you talk about all of the questions
and thoughts that are running through your mind?

Or maybe you have a loved one that has been living with the effects
of congenital CMV for years and you just want to share your story,
share some photos, and link up with other CMV Families.

Maybe you want to lend support to those new CMV Families by way of sharing tips....
how to navigate the health systems with a special needs child, how to create your
own special needs "equipment" for your child by using non-special needs items,
all things big and little but simply just to share and communicate with each other.

We can be there for each other
and now our Foundation has provided the forum to do just that!
Click on the Facebook link below to go to the
Brendan B. McGinnis Congenital CMV Foundation's page on Facebook.
You can post questions, stories, photos and connect with other CMV Families.
We will keep our events tab updated on that page as well.
We hope you find this new feature helpful in many ways!

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.

Brendan B. McGinnis
Congenital CMV Foundation

If you are considering having a baby,
you need to know about congenital
cytomegalovirus (CMV) infection !

Connect with other CMV Families

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)

Brendan B. McGinnis Congenital CMV Foundation |