Turner Syndrome Society of the United States (Tssus)

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.



Hi everyone!

#StandForSomething

My name is Harper Daisy, and I have a rare genetic disorder called Turner Syndrome. TS is caused by the deletion or partial absence of the second X chromosome. This means my body is missing the genetic material which helps my body grow, develop and mature naturally. Along with this, I also have mental health issues and autoimmune disorders. Did you know that it's estimated that only 2% of TS babies survive to full gestation? I am a miracle!!

Would you like to join me in making a difference? I am raising money to benefit the Turner Syndrome Society of the United States (TSSUS), and any donation will help create an impact. Thanks in advance for contributing to this cause that means so much to our family.

My Lemonade Stand will be at FIT @ Stonebridge Ranch (7250 Virginia Pkwy McKinney, TX 75071) on Saturday, 10/15, from 10 am—12pm. There will be food, music, raffle prizes (please bring money for tickets), a bounce house and so much fun!

We hope to see you there!

For more information about Turner Syndrome, please visit the website at https://www.turnersyndrome.org

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.

Want to join me in making a difference? I'm raising money to benefit Turner Syndrome Society of the United States (Tssus), and any donation will help make an impact. Thanks in advance for your contribution to this cause that means so much to me.

More information about Turner Syndrome Society of the United States (Tssus): The mission of the Turner Syndrome Society of the United States is to advance knowledge, facilitate research, and provide support for all those touched by Turner syndrome.