Español | Arabic |
Bulgaria |
China |
Croatian |
Czech |
Danish |
Dutch |
Finnish |
French |
German |
Greek |
Hindi |
Italy |
Japan |
Korea |
Norway |
Romania | Polish |
Russia |
Portugal |
Sweden |
|
|
2009: We Commemorate 35 Years of Awareness, Research, & Service Saving the Lives of Children. |
Organization Links | Information | Reye's Links |
|
The Foundation's Programs 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
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. The Foundation's Top Objectives are: ... AWARENESS - to aid in early detection and educate the public and medical communities about the risk involved with using aspirin and other salicylates. ... SERVICE - to provide emotional support and guidance to families experiencing the trauma of Reye's Syndrome. ... RESEARCH - to support investigation into the disease's cause, management, treatment and prevention, as well as study its impact on survivors. If this site has proved helpful to you, a donation from you would assist us in keeping this site up-to-date. To make a tax deductible donation to the National Reye's Syndrome Foundation, click here. To become a member of the National Reye's Syndrome Foundation, click here. Know that your donations and memberships allow us to continue spreading Awareness about Reye's Syndrome to new mom's, new medical professionals, caregivers, schools, daycare centers, churches, and immigrants, and to a global population who can now access this website. You make a difference, a life and death difference. -- Thank You. |
|
Privacy Policy | Disclaimer | Site Map |
The National Reye's Syndrome Foundation neither seeks nor receives government grants or funds for services rendered and depends totally on voluntary contributions for support of all programs. |
© 1974 thru 2009 National Reye's Syndrome Foundation Inc. All Rights Reserved |
Site Design Donated, Maintained, and Managed by Interim Business Services LLC |