Fragile X is a genetic disorder that affects 1 in 4,000 men. We are currently enrolling men with fragile X for a study at the NIH Clinical Center. Watch this short video to learn more about the study. Email: loutaev.inna@nih.gov or call 1-301-496-4707 [TTY: 1-866-411-1010]. | National Institute of Mental Health

🧬 How is Fragile X Syndrome Inherited? �It’s one of the first - and most important - questions families ask after a diagnosis. In just two minutes, we break down the basics. Understanding genetics can feel overwhelming, especially when it affects the people you love. Whether you’re newly diagnosed or supporting someone who is, this is a must-watch. ��#fragilex #fragilexawareness | The National Fragile X Foundation

Meet Mack Feldman! He has Fragile X syndrome, and his parents are Abby Gaunt and Gabe Feldman. Abby and Gabe, “support the National Fragile X Foundation because they've been there every step of the way since Mack's diagnosis. They've helped connect us to other families who are living with Fragile X syndrome. They've introduced us to the work of leading Fragile X experts and they host the most incredible conference every other year.” Abby and Gabe support fellow Fragile X families by volunteering