The VACTERL Network: Sharing similarities - Celebrating differences.


The VACTERL Network was established to provide support to families who have a child born with VACTERL/VATER or adults with VACTERL. The purpose of our organization is to share resources, tips and information among the families. We are a resource to individuals to help make the journey with VACTERL as easy as possible.


For additional information, contact President Josie Quijas at mandjq1989@yahoo.com.


Special note: Our 5th VACTERL Family conference is coming up in June 2009 in Philadelphia, PA. Here is a link the date and hotel information - http://www.vacterlnetwork.org/conference.html. We will post a speaker listing, schedule of events and a registration form when more information becomes available.