Our mission is to provide information and support services to families affected by Dyskeratosis Congenita worldwide, to encourage the medical community's research in finding causes and effective treatments, and to facilitate improved diagnosis by educating medical providers.
Disclaimer: Medicine is a constantly changing science and not all treatments are clearly established especially with such a rare disease. New research changes drug and treatment therapies daily. The authors, editors, and publisher of this website have used their best efforts to provide information that is up-to-date and accurate and is generally accepted within medical standards at the time of publication. However, as medical science is constantly changing and human error is always possible, the authors, editors, and publisher or any other party involved with the publication of this article do not warrant the information in this article is accurate or complete, nor are they responsible for omissions or errors in the article or for the results of using this information. They are also not responsible for any of the statements made by individuals posting their own stories or experiences on this site.

DC Angels--In Memory Of Our Loved Ones
Irene Nef Schulte
Feb. 23, 1930--Oct. 24, 1992
Dilan Phillips
April 5, 1992--Sept. 16, 2006
Joseph Scott "Joey" IngramĀ 
July 15, 1979--Feb. 4, 2009
Josh Friedman
June 24, 1994--Nov. 18, 2011
Aileen E. Fearon
Aug. 30, 1996--Jan. 6, 2013
Ayelet Galena
Nov. 2009--Jan. 31, 2012
If you would like your "angel" remembered here please send their photo and name and dates to snaca6@aol.com
McKenzie Lain Bedingfield
Oct. 4, 2001--June 4, 2013

Jorge Fernandez
2008--Dec.11, 2013