Press Releases

July 25, 2011 – SJS Awareness Walk August 13, 2o11

March 15, 2010 – A Baby’s Fight for Life Is a Teen’s Story of Survival

June 16, 2008 – Stevens- Johnson Syndrome Website For Kids Launched By Julie McCawley

August 1, 2007 – Stevens-Johnson Syndrome Awareness Month August 2007

October 25, 2006 – Local Non-Profit Organization to be Featured on the Montel Williams Show

December 31, 2004 – Statement Issued by Stevens-Johnson Syndrome Foundation regarding Lawsuit Against Makers of Children’s Motrin

Dec 10, 2004 – Rising Prescription Drug Use Corresponds to Increase in SJS

July 22, 2002 – Stevens Johnson Syndrome Foundation Issues Warning Signs

The Stevens Johnson Syndrome Foundation (Julie Foundation for allergic drug reactions) is a non-profit organization. The purpose of the foundation is to provide the public and medical communities with information on adverse allergic drug reactions.
Our goal is to make the public aware of adverse reactions, so that a quick diagnosis may be made and the offending drug stopped as soon as possible.