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National Reye's Syndrome Foundation
Disclaimer:
The contents of the National Reye's Syndrome Web Site, such as text, graphics, images, and other material contained on the National Reye's Syndrome Site ("Content") are for informational purposes only. The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.
Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on the National Reye's Syndrome Site!
If you think you may have a medical emergency, call your doctor or 911 immediately.
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Reye's Syndrome, a deadly disease, strikes swiftly and can attack any child, teen, or adult without warning. All body organs are affected, with the liver and brain suffering most seriously.
While the cause and cure remain unknown, research has established a link between Reye's Syndrome and the use of aspirin and other salicylate containing medications, over the counter products, and topical use products.
In 1974, the National Reye's Syndrome Foundation was incorporated, becoming the first citizen group to generate a concerted, organized lay movement to eradicate Reye's Syndrome.
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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.
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