Please help the NFXF and the Fragile X clinics gather the information necessary to support clinical trials in Fragile X syndrome (FXS) across the country. These studies are designed to find out if medicines commonly prescribed to persons with FXS provide real, meaningful benefits to individuals and families.
Please answer a few questions (takes about a minute or two) to complete our survey.
Note: Please complete ONLY if you are the parent/guardian of a child/adult with FXS who is at least one year old.