The Sean W. Venezia Foundation
is a non-profit, all-volunteer,
501(c) (3) organization.
Helping Fund the Fight Against Spinal Muscular Atrophy

The #1 Genetic Killer of Children Under the Age of 2

Spinal Muscular Atrophy, commonly referred to as SMA, is an inherited disease that destroys the spinal cord nerves that control muscle movement, which affects crawling, walking, head and neck control, and even breathing and swallowing. Although SMA is as common as ALS (Lou Gehrig's Disease), it is not nearly as well-known because many of its victims die so young.

Currently, there is no treatment or cure for SMA. However, its cause is well understood and the "problem" gene has been identified. As a result, a cure could be on the horizon, but money is still needed to fund research and to help families that are currently impacted by this tragic disorder.


Make Your Online Shopping Count

The next time you shop online with your favorite retailer, you can have a percentage of your purchases donated to: The Sean W. Venezia Foundation.

Best of all - it's fast, easy, and FREE to do. Learn more.





Sponsor The Venezia Family in this year's Walk-n-Roll to cure SMA.

If possible, come out and show your support.

Where: Details to follow
Be sure to check back soon

SPONSOR US TODAY!

Sean W. Venezia
9 months on earth. Forever in our hearts.


On October 20, 2003. Sean died from complications associated with SMA.
View a one-minute clip of Sean's video and get to know a little boy whose very short life was filled with nothing but love.