My Nonprofit Reviews

When we lost our daughter suddenly to a previously undetected heart arrhythymia on June 20,2005, we had no where to turn. Because long qt is such a rare disorder there was little support for those afflicted. While searching the internet we came across the SADS website. We have found that SADS has a wealth of information and reaches out to those who suffer a loss such as ours. We have also attended some of their conferences and have learned so much from their knowledgeable experts. We feel SADS is such a valuable organization and have held an annual fundraiser with proceeds going to them since 2006 to help raise awareness. Our fundraiser is called Christie's Heartoberfest. We have rasied over $100,000 for SADS and will continue to do so in the future.

More Feedback