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Links: Treacher Collins Syndrome - International - Medical Condition

Amie's Homepage

I have told a little about my life with TCS and what TCS is. There is an essay written by one of my close friends, several pictures, a TCS message board, and a few other things.

Glenn Whicker Family

Katie has the most wonderful personality! She makes the whole world happy. Come join in the Treacher Collins discussion group to learn more what your options are from those who have been through it.

HUM-MOLGEN Bulletin Board - Free Newsletter

International Birth Defects Information Systems

Birth Defects are the major cause of infant mortality and a leading cause of disability. Birth Defects can be prevented. Early intervention is important to ameliorate the consequences of birth defects and requires accurate diagnosis and understanding of causes.

International Craniofacial Institute - Cleft Lip & Palate Treatment Center

Treacher Collins Preoperative frontal view of 16-year-old patient with Treacher Collins Syndrome. No previous correction had been performed. Postoperative lateral view 1 year after orthognathic surgery. Pre and postoperative lateral views of same patient. Every patient's case is unique. Please contact us for a consultation.

The National Craniofacial Association

Excellent web site which explains the syndrome and also lists useful contacts

The Treacher Collins Foundation

The Treacher Collins Foundation is an organization of families, individuals, and professionals who are interested in developing and sharing knowledge and experience about Treacher Collins syndrome and related conditions.

The Treacher Collins Network

Thanks for stopping by. We would like to apologize for the delay in the update. There have been serious medical issues at home and we were just not able to update as we would have liked. We are currently updating all pages, so please be patient. We wish to dedicate this page to our daughter, Katilyn Gabrielle. Our hope is that one day, we may rid ourselves of the "normal" societal standards that we hold so dear, and embrace the differences, whatever they may be, that make our lives richer. Katilyn, we love you, and pray that one day, we will meet again. Not in our arms but, forever in our heart.

Treacher Collins Family Support Group

UCDavis Children's Hospital - Cleft & Craniofacial Program

The physicians and specialists of our interdisciplinary team are committed to providing quality, comprehensive, coordinated care to pediatric patients with cleft and craniofacial problems and ongoing support to their families. Our treatment program combines the best in state-of-the-art surgical and therapeutic techniques with a sensitive, caring approach. We recognize the special problems faced by our young patients, and we are dedicated to working with them and their families as partners for optimal results and healthier futures.
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