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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
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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
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