Hi I’m Hannah Jones. I was born with a chromosomal abnormality called Turner Syndrome. Turner Syndrome, or TS, refers to a missing chromosome in females (part of the second X chromosome in some or all cells.) The most visible sign in people with TS is that we're usually a little shorter than most people. 

Having Turner Syndrome has meant a good amount of medical concerns since a very young age. I give lots of credit to modern medicine in helping overcome a lot of the congenital issues I had to make me who I am today.

The Turner Syndrome Society advances knowledge, facilitates research and provides support for all persons touched by Turner syndrome.  The Turner Syndrome Society relies on donations, grants, and sponsorships to create awareness of TS across the nation, to promote TS research conducted by clinicians, and to support every life touched by TS through local groups, national conference, website resources, and more.  We greatly appreciate every dollar gifted to them to help them support girls like me.

Thank you!

Hannah