My Nonprofit Reviews

My family was introduced to Turner Syndrome when my little sister, Amanda, was diagnosed with TS when she was 8. Over the last 12 years, I have watched my mother, Laura Fasciano, put her heart, soul, blood, sweat, and tears into creating an organization that aims to provide everything possible to those directly or indirectly affected by Turner Syndrome, both young and old.
TSF has fostered a welcoming and embracing community, continually delivers a greater collective of research, brings medical professionals together for collaboration, and provides its members with greater ease of access that research and data.
Witnessing the impact this organization has on others is awe-inspiring. As the old adage goes - "She believe she could, so she did"!