Fragile X- Associated Disorders (FXD)
If you have just found out through prenatal testing that your baby has a Fragile X-Associated Disorder (FXD) or may have a FXD, or if you have just learned that you are a carrier of Fragile X and are looking for more information, the Genetic Support Foundation is a good starting point.
There are other important resources out there, including your doctor and genetic counselor. We have also compiled a list of resources below that can provide you with additional information and support.
After reviewing the information below, if you have a question that you are having difficulty finding an answer for, please feel free to contact us