Join us for a powerfully meaningful evening of conversation during Turner Syndrome Awareness Month. Through personal stories and shared reflections, panelists will speak about what it’s really like to live with Turner syndrome, navigate diagnosis and care, and build resilience along the way. Attendees will also have the opportunity to ask questions and engage in discussion.

Whether you are part of the Turner syndrome community or seeking to better understand it, we invite you to join us for an evening of connection, learning, and shared experience.
Registration required. We hope to see you there.

This event is open to patients, parents, caregivers, advocates, and anyone looking to learn more about Turner syndrome through real-life perspectives.

Facilitator Stacie Pelton
Panelists

Jean-Marie Andrews, TS mom
Kaitlin Yaska, woman with TS
Carlee Ritch, woman with TS

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-based. In addition to our online resources, we provide personalized one-on-one support to everyone who calls or emails our office each day. 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 chosen to support us by joining the TSF Professional Membership, an initiative that provides 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 builds a future of hope, awareness, and care.

WE- TSAM 2026 Patient & Parent Panel

By TURNER SYNDROME FOUNDATION INC

WE- TSAM 2026 Patient & Parent Panel

Donations and sponsorships make learning events such as this WE LEARN webinar activity provided freely and accessible to everyone. Please support today!