Turner Syndrome Research & Awareness 2025

Happy Turner Syndrome Awareness Month!

TS is a rare genetic disorder that is caused by a partial or complete loss of an X chromosome.

TS affects about 1 in every 2,000 births.

2% of babies with TS make it to full term.

Our daughter, Palmer, was diagnosed with Turner Syndrome at birth. She is now 3 years old and thriving! Palmer is our social butterfly…she’s the perfect combination of funny, sweet & wild.

This is our 4th year to raise money for the Turner Syndrome Society in honor of our sweet miracle girl. This year our goal is to raise $1,800 (or more ).

⁉️ How can you help ⁉️

DONATE! We’ve set up a GoFundMe account that is directly linked to the Tuner Syndrome Society.

DRINK! Nutrition 33 is helping us celebrate TS awareness month! They have made TWO special teas in honor of Palmer!

Princess Palmer

Social Butterfly

A portion of each drink sold during this month will be donated to the Turner Syndrome Society.

The Turner Syndrome Society relies on donations, grants, and sponsorships to advance knowledge, create awareness, facilitate research, and support every life touched by TS.