1938 Collective Monthly Giving
A Missing Chromosome Shouldn't Mean Missed Opportunities
Honoring the year Turner Syndrome was first documented, the 1938 Collective is a monthly giving community championing women, girls, and all people affected by TS!
Monthly giving sustains our work!
1 in Every 2,000 Females is Born Into a Life of Questions
Her life begins with an invisible genetic condition that most people — including doctors — don’t understand. Turner syndrome (TS) affects every part of her life: growth, heart health, fertility, social connection, learning, and emotional well-being. The reality is, living with TS means constantly searching. For answers. For treatment. For a world that supports her complex journey.
Together, we can give her hope—and answers.
Introducing: The 1938 Collective
The 1938 Collective (named for the year TS was first discovered) is our monthly giving community committed to ensuring:
- More people are made aware of Turner syndrome
- More doctors are educated to provide continuous care
- Resources are always there for girls, women, and families navigating TS
Your monthly membership makes life with Turner syndrome easier and brighter. Every month…
$19.38 honors the year TS was featured in medical literature
$36 provides TS education for healthcare providers
$60 fuels international awareness in 60 countries
$92 supports research that paves the way for medical breakthroughs
What It's Like In The Collective
You’re proudly donating the cost of one lunch or dinner out each month. That gift helps fill a pool that pours directly into the daily lives of people with TS.
In the 1938 Collective, you’re part of something bigger than yourself: a movement of individuals with TS, affected families, medical providers, and allies who will make this genetic disease better understood.
As a thank you for your monthly support, get ready to receive:
Video Updates
You’ll get an exclusive 1938 Collective video update once a month with success stories and advocacy opportunities.
Discounted Swag
1938 Members receive a year-round 10% discount on all Turner Syndrome Foundation swag items so you can raise awareness!
Annual Meeting
Once a year, 1938 Collective members convene virtually to celebrate our wins and contribute to TSF’s vision.
Collective Member Spotlight: Meet Amy
“My daughter Calla was diagnosed with Turner Syndrome at 13. We were lucky to have a dedicated TS clinic nearby, but every family should have that kind of care. I give to TSF to help raise awareness, educate providers, and ensure every girl and woman with TS gets the support she deserves.
Over the years, we’ve learned that the TS community often knows more about the condition than many in the medical field. While we were fortunate to have access to the Turner Syndrome clinic at Seattle Children’s, specialized care like this should be available in all 50 states. Because TS is rare, it isn’t always a priority for research — but that needs to change.
I give to TSF because I believe in building awareness, educating providers, and ensuring that every girl and woman with TS has the care, understanding, and support she deserves. My hope for the future is a world where the medical community is well-informed and where those living with TS are surrounded by unwavering support.”
Your Monthly Gift Does More Than You Know
Whether Turner Syndrome affects you personally, a loved one, a patient, or a neighbor, thank you for believing in the power of the Collective to create a future with fewer questions and more opportunities.
Manage Your Recurring Donation –Â To manage your recurring donation go to the bottom of the email receipt and click the ‘manage your recurring donation’ link. There you can change the amount, recurring series, and credit card. You may cancel your recurring donation at any time.
