Was your loved one recently diagnosed? We are here to help you navigate this challenging time.
Join the community for a cure to get the latest on research and to learn how you can take action for a cure.
Our singular focus is to find a cure for Rett syndrome, and we will not rest until we achieve it.
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Updates on research progress, biopharmaceutical company news, Rett community happenings. Frequency: once every two months
Information specifically for caregivers and family members, including clinical trial information, medical care, ways you can support our funding efforts, and messages from our CEO and staff. Frequency: once every two months
Immediate updates on Rett research and drug development updates and notifications about ways to get your loved one involved in research studies. Frequency: whenever there is news to share, we won’t inundate you
All of the funds raised at RSRT can be traced back to a Rett family and their network. Collectively our global community has the power to speed the timeline for a cure. Get information on how you can get involved in raising funds. No matter where you live or what language you speak you can have an impact. Frequency: a couple times a month maximum