My daughter was diagnosed with Turner Syndrome when she was 4 years old, she is 10 now. I reached out to the Turner Syndrome Foundation because I felt lost and alone. They have been a blessing to us! We’ve learned so much about the syndrome. We are now supported by a great community, have tons of information and resources to help our little girl, and to help others learn too – from friends, family, teachers, to doctors!
Thank you so much for being there for us!!!