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Children, teenagers, and adults are dying of Reye's Syndrome. The Foundation is committed to the health and well-being of those who are most at risk. The Foundation has made great gains toward our ultimate goal of eradicating Reye's Syndrome. Our public awareness programs have resulted in a decrease in the number of cases reported in recent years. It is hoped that continuing that awareness will bring us closer to our goal. Awareness - to aid in early detection and to educate the public and medical communities about the risk factor involved with the use of aspirin. To conduct awareness programs, the NRSF has brochures, bulletins, television and radio public service announcements, documentary and video/DVD presentations, and a speakers bureau available to groups and organizations free of charge. Service - to give the families experiencing the personal trauma of Reye's Syndrome emotional support and guidance. Research - to support investigation into the cause, management, treatment, and prevention of the disease, as well as study the impact the disease has had on survivors. Major Accomplishments of the NRSF * Encouraged and supported mandatory warning labels on all over-the-counter medicines containing aspirin. Research The Foundation established a Scientific Advisory Board (SAB) comprised of eight medical scientists from various parts of the United States and Canada, many of whom have been active in Reye's Syndrome research. The Scientific Advisory Board is chaired by Dr. Thomas H. Glick, Associate Professor of Neurology at Harvard Medical School, and Chief of Neurology at The Cambridge Hospital, Cambridge, Massachusetts. National Reye's Syndrome Foundation, Inc. |
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