Pull-thru Network (PTN) was founded in 1988 and has grown to be one of the largest organizations in the world dedicated to the needs of those born with an anorectal malformation or colon disease and any of the associated diagnoses. These diagnoses include:
♦ Imperforate Anus ♦ Cloaca ♦ Cloacal Exstrophy ♦ Anal Stenosis ♦ Bladder Exstrophy ♦ VACTERL/VATER Association ♦ Hirschsprung's Disease ♦ Tethered Spinal Cord ♦ Neurogenic Bladder ♦ Caudal Regression ♦ Down Syndrome and ♦ others
Despite the differences in diagnoses, the members of Pull-thru Network are bound together by a common need for information, education, support and advocacy for families, children, teen and adults who are facing the challenges of these diagnoses. We invite you to take a look at the programs and services provided by Pull-thru Network and encourage you to take advantage of all that is available by becoming a PTN member. Membership is required for participation in many of the features of this website. By requiring membership, Pull-thru Network is protecting your and your child's privacy while facilitating an open exchange of information between members.
If you have any questions, or need additional information, please do not hesitate to let us know. Contact us at: firstname.lastname@example.org Phone: 309-262-0786
Lori Parker, Executive Director, Normal, Illinois
Hollie Filce, Associate Director, Hattiesburg, Mississippi
Carmell Burns, Director, Paradise, Utah
Tenley Gritts, Director, Chula Vista, California
Tricia Mihalic, Director, Traverse City, Michigan
NEW2016 Pull-thru Network Family Conference!
July 14-17, 2016
See conference page for details, registration and hotel information
Want to plan a social for PTN members in your area? Email us at email@example.com. We can help support your gathering!
PTN Member Chat
We are no longer holding monthly chats on the website. This is a temporary action. Updates on future chats will be posted here.