Welcome to the Minnesota Rett Syndrome Research Association!
It is the mission of the Minnesota Rett Syndrome Research Association to fund important Rett Syndrome research initiatives, and promote wellness and education of families within our community that are affected by Rett Syndrome.
Updated Section: Meet the MRSRA Board Members
In an effort to add content and update the MRSRA website, there is now an updated section on the MRSRA Board Members here.
Help us make the MRSRA site better, and more useful! Please submit your comments and suggestions on what you'd like to see more of, less of, some of or none of on the website!
Where we are
New
Google Map shows where Rett families are distributed throughout the
state.
Click here to be taken to the new Google Map, which shows the communities where those known to MRSRA with Rett Syndrome live.
Please note that the map does not show specific addresses or locations of families in order to protect privacy. Locations shown only indicate the community where the family/individual lives.
Research to Reality
Click on the link to donate to the International Rett Syndrome Research Foundation, as all donations will be matched up to $1 million by the Pioneer Fund.
International Rett Syndrome Foundation - Research to Reality Campaign page
International Rett Syndrome Foundation -Research to Reality Campaign FAQ
Don’t delay - thousands of girls and women with Rett syndrome are waiting!
Thank you for your support!