Before someone is diagnosed with Fragile X syndrome, all of the signs are there, but it can take a while to see Fragile X. If your child has unexplained developmental delays, ask about a simple blood test to confirm or rule out Fragile X. Because it is a genetic disorder, knowing is important not only to your child but to past and future generations. Learn more about testing at https://hubs.ly/H0t1Bmj0. | The National Fragile X Foundation

🧬 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