In 2006, the WTC Health Registry published its first research papers. 18 years later, Registry analysts have published over 185 papers that have helped create guidelines that can save lives and inform new policies and treatments.
For 20 years, the World Trade Center Health Registry has remained committed to researching and understanding the long-term health impacts of those exposed in the aftermath of 9/11 and assisting its Registry enrollees in getting care.
Nearly 20 years later, researchers have documented the increasing risk concerning cognitive dysfunction including Alzheimer’s. This risk has been associated with both physical exposures at the World Trade Center and chronic post-traumatic stress disorder
A community leader, a 9/11 survivor and a World Trade Center Enrollee. From appearing on recruitment posters to working tirelessly to sign up volunteer enrollees, Paul has spent the last twenty years as an advocate for the Registry.
Learn about eligibility and how to get monitoring and treatment for 9/11-related health care for enrollees and their families
Registries allow researchers and health professionals to track and investigate illness and recovery related to disasters. Lessons learned from a disaster can also save lives and reduce injuries in future disasters. The federal Agency for Toxic Substances and Disease Registry and the New York City Health Department established the World Trade Center (WTC) Health Registry in 2002 to monitor the health of people directly exposed to the 9/11 WTC disaster. The Registry became the largest post-disaster registry in U.S. history when more than 71,000 responders and survivors voluntarily enrolled in 2003-04. Since May 2009, the Registry has been funded by the National Institute for Occupational Safety and Health and has ongoing collaborations with academic and governmental entities and medical institutions.
The WTC Health Registry periodically follows-up with enrollees to track changes in physical and mental health over time and gaps in care.