Join Us in Making a Difference for Turner Syndrome

The Fasciano Family Fund is proud to support the Turner Syndrome Foundation, and we invite you to stand with us in this vital mission.

Amanda was in our hearts long before she was born—a true blessing in our lives. She has taught us about love, resilience, and the power of unwavering support. When she was diagnosed with Turner syndrome at age seven, it was a difficult reality to face. But through this journey, we have been blessed to meet extraordinary people who have empowered us to become proactive advocates. The best advice we ever received was simple yet profound: be open, be honest, and never withhold the truth. With 100% family support and a willingness to embrace help, we have learned that even the toughest challenges can be met with love and strength.

In 2009, Laura Fasciano founded the Turner Syndrome Foundation in honor of her family, driven by the mission to advance research, awareness, and support for those affected. Through our website, social media, and direct outreach, TSF provides free education, advocacy, and resources to individuals and families worldwide. But we cannot do this alone.

Turner syndrome is a women’s health issue that deserves greater attention and stronger support. Too many individuals are struggling in silence, and we need to change that. With your help, we can continue to fund research, advocate for better healthcare, and provide hope to those navigating this journey.

Please stand with us. Show your compassion, make a difference, and donate today. Every contribution brings us one step closer to a brighter future for all those affected by Turner syndrome.

Thank you for your generosity and support.