Can you imagine waiting years to hear your child talk?

For many families with Fragile X, waiting years to hear your child talk is their reality. Ty Wieber relied on others to be his voice for the first six years of his life. Thanks to your support, FRAXA-funded research laid the groundwork for a clinical trial that changed Ty and his family’s world forever. During the trial, Ty spoke his first words. Your investment in FRAXA funds life-changing research for those living with Fragile X syndrome. We need you! Make a gift today. https://www.fraxa.org/annual-appeal/ FRAXA’s mission is to find effective treatments and ultimately a cure for Fragile X syndrome. We directly fund research grants and fellowships at top universities around the world. We partner with biomedical and pharmaceutical companies, large and small, to bridge the gap between research discoveries and actual treatments. Treatments for Fragile X are likely to help people affected by autism, Alzheimer’s, and other brain disorders. To learn more about FRAXA's Fragile X syndrome research, to get involved with Fragile X awareness and events or to donate to FRAXA research, visit www.fraxa.org Let's Connect Facebook:   / fraxaresearch   Instagram:   / fraxaresearch   LinkedIn:   / fraxa-research-foundation   Twitter:   / fraxaresearch   Website: https://www.fraxa.org