Recognized as one of the largest, leading SIDS organizations in the country, the CJ Foundation was founded in 1994 by Joel and Susan Hollander in memory of their daughter, Carly Jenna, who died from SIDS in 1993. Since its inception, the CJ Foundation has provided millions of dollars towards SIDS research projects, organizations, support programs and public education and awareness campaigns throughout the nation, making tremendous strides in its fight to eliminate SIDS.
Today, the Foundation is the largest non-government funder of programs meeting the needs of the SIDS community. The CJ Foundation contributes its resources to the nation's leading SIDS investigators. As research has indicated that risk reduction is possible, the CJ Foundation is committed to developing, implementing and providing funding for education and awareness programs so that the message of risk reduction reaches every potential population. The CJ Foundation is national in scope and also supports bereavement and counseling services for those families that have lost a baby to SIDS.
Additionally, in 2001, the CJ Foundation created the Sudden Unexplained Death in Childhood (SUDC) Program. SUDC is the sudden and unexplained death of a child over the age of twelve months. Its mission is to provide a centralized resource for information, support and advocacy for a community that, without the support of the CJ Foundation, would have remained unnoticed.
We are located in the WFAN/Imus Pediatric Center at Hackensack University Medical Center.