Join TSF for a peer-to-peer panel discussion designed for expectant parents and families navigating a prenatal diagnosis of Turner syndrome.

In this conversation, three mothers of girls with Turner syndrome will share their personal experiences receiving their daughters’ diagnoses during pregnancy. Panelists will discuss the emotions and uncertainty that can come with diagnosis, navigating pregnancy after receiving the news, preparing for their daughters’ arrivals, and their experiences during the early years of life.

This event is intended to provide connection, perspective, and support through shared lived experience.

Meet the Panelists

Rena'e Williams: Rena’e is the mother of Shekina, a 1-year-old with Turner syndrome. She received Shekina’s diagnosis at five months pregnant.

Maurissa Trent: Maurissa is the mother of 9-year-old Juliana.

Briana Rex: Briana is the mother of Lyla, a 1-year-old with Turner syndrome who is also a fraternal twin.

Facilitated By Stacie Pelton: Stacie is a woman with Turner syndrome, a social worker, and a dedicated volunteer with the Turner Syndrome Foundation.

About the Panel Series

TSF Panel Events are peer-to-peer conversations where individuals and families can learn from the experiences of others navigating different aspects of life with Turner syndrome. These events feature community members, parents, and occasional subject matter experts sharing personal stories, practical insights, and audience Q&A in a supportive environment.

Registration is free but required. Register to receive the Zoom link.

This event will be recorded.

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- Expectant Parent Panel

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