Summer Fun with Friends!

A Day of Connection, Nature, and Community

Join the Turner Syndrome Foundation for a meaningful one-day retreat designed for girls, women, and families living with Turner syndrome. Set in a peaceful, nature-based environment, this experience offers something rare and powerful: the opportunity to connect with others who truly understand the journey.

For many, this is more than an event—it’s a turning point.

Event Details

📍 Location: Liberty Lake Picnic
Bordentown, New Jersey

📅 Date: Saturday, July 18, 2026
⏰ Time: 12:00 PM – 5:00 PM (EST)

Rain or shine, the event will take place as scheduled.

Why This Retreat Matters

Living with Turner syndrome often means navigating complex medical needs, emotional challenges, and, at times, isolation. Because the condition is rare, many individuals never meet someone who shares their experience.

This retreat changes that.

Participants will:

Build genuine, lasting friendships
Strengthen confidence and independence
Learn practical life and health insights
Experience the relief of being seen, understood, and supported

As many attendees describe, it is life-changing.

What to Expect

This one-day retreat is designed to foster connection in a relaxed, welcoming outdoor setting.

Highlights include:

Community-building activities and group engagement
Outdoor recreation, including swimming, games, and more
Shared meals and informal networking
A supportive, inclusive atmosphere for all ages

This is a community-focused experience—centered on connection, conversation, and simply enjoying time together.

Registration Information

Registration includes:

Full access to retreat activities
Meals and refreshments throughout the day
Entry into a safe, welcoming community experience

⚠️ Capacity is limited to preserve a high-quality, connected experience. Early registration is strongly encouraged.

🎟️ Scholarships are limited and reserved for individuals with Turner syndrome. Availability is based on need and supported by donor funding.

Join the Turner Syndrome Foundation for its Annual Community Day for fun in the sun at Liberty Lake Picnic in Bordentown, NJ. Rain or shine, the event will go on!! This event is for all ages and is a great way to meet new people!

Community Social!
This will be a strictly social and friendly networking event! Individuals and families affected by TS are invited to spend the day together, interacting and having fun. Talking among yourselves and as a group. There will be no professional medical presentations. We want to get to know you and you to get to know one another!

There will be fun!
Activities include enjoying the great outdoors with games, swimming, mini golf, good food, new friends, and more! There are two pools and dressing rooms, so be sure to bring your towels & swimsuits! Food and drinks are provided all day, right under our pavilion, with gluten-free options available upon request. Coolers are permitted (no glass bottles, please). Surrounded by nature, nestled under a covered pavilion reserved just for our group, you will find ample tables, shade from the sun, and seating.

Registration:
Event registration includes entrance to the park for the Turner Syndrome Foundation's Community Day and meals. Family and friends are welcome to join the TSF Community Day. You can sponsor the event to support TSF in providing a limited number of free event tickets for individuals with TS. Please support our efforts by sponsoring this event so everyone can enjoy this day!

Overnight Accommodations

While this is a one-day retreat, guests traveling from outside the area are welcome to extend their stay.

A curated list of nearby hotels and accommodations in the Bordentown area will be provided upon registration to help you plan your visit with ease.

Become a Sponsor: Make This Experience Possible

Families affected by Turner syndrome often face significant financial burdens due to ongoing medical care. Experiences like this retreat can be out of reach without support.

Your sponsorship helps ensure that no one is excluded because of cost.

When you sponsor this retreat, you are:

Providing access for individuals who otherwise could not attend
Creating a space for emotional healing and connection
Supporting confidence, independence, and lifelong relationships
Strengthening an entire community

💡 Demand for scholarships exceeds available funding each year. Your support directly expands access.

Sponsorship Opportunities

We invite individuals, organizations, and partners to support this impactful event.

Options may include:

Sponsored attendee tickets
Family sponsorship packages
Activity or experience sponsorships
General event support

Sponsors will be recognized as key partners in making this retreat accessible and meaningful.

Be Part of the Experience

Whether you attend, sponsor, or share this opportunity, you are helping create a space where individuals with Turner syndrome feel empowered, connected, and hopeful.

Together, we can turn one day into a lasting impact.

Register early to secure your spot or sponsor today to expand access.

Registrations are non-refundable and non-transferable. A limited number of scholarships are available for individuals in need. If you have questions, please call (732) 847-3385 for assistance.

Turner Syndrome affects 1 in 2,000 females. We can help.

Mission Statement:
The mission of the Turner Syndrome Foundation (TSF) is to support research initiatives and facilitate education programs that increase professional awareness and enhance medical care of those affected by Turner syndrome. Early diagnosis and comprehensive treatments over the lifespan may lead to a brighter and healthier future for all young girls and women with Turner syndrome. TSF is a registered 501(c)(3) nonprofit organization

What Makes TSF Different?

Free Resources. Personalized Support. Dedication to Research & Education.

Our philosophy to keep life-changing resources free and accessible to patients is a key component of what sets us apart. We do not require membership dues or fees to access our resources. Everything on our website is free for everyone, so you can find what you need exactly when you need it.

In fact, most of our events are free to attend, including our patient education workshops. These workshops feature presentations by experienced medical professionals – and are 100% donation run. In addition to our online resources, we provide personalized one-on-one support to every individual who calls or emails our office. We are proud to offer this level of support to the most vulnerable members of our community.

However, these elements only begin to scratch the surface of what makes us unique. While we understand and appreciate the importance of community events and fundraisers, we also know that research and education initiatives will be more impactful in the long term. Our mission to “support research initiatives and facilitate education programs that increase professional awareness and enhance medical care” means that we partner with medical professionals, industry leaders, and more to form councils, publish guidelines, and support research.

Our commitment to research and education is demonstrated by the strong support of the medical community. TSF is regarded in the medical community as a leading resource for Turner Syndrome. Professionals often refer their patients to TSF because of our many enriching resources. Many medical professionals have even chosen to support us by joining the TSF Professional Membership, an initiative formed to provide support to patients who need it most.

With all of this in mind, turn to the Turner Syndrome FOUNDATION. A strong foundation of free support, education, and research lays the groundwork for a future of hope, awareness, and care.

Turner Syndrome Annual Retreat July 18, 2026

A calming holistic adventure in nature