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Testimonials

Behind every SLC6A1-related neurodevelopmental disorder (SLC6A1-NDD) diagnosis is a person, a family, and a unique story of challenges and hope.

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SLC6A1-NDD affects each individual differently, with symptoms and severity varying from person to person. Through the following testimonies, families offer a glimpse into what life with the condition can look like and how it may affect everyday life.​ Some of the videos may be difficult to watch, particularly for families whose loved ones have just recently been diagnosed.

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Every story strengthens our determination to work together towards a future in which effective treatments are available to everyone affected by SLC6A1-NDD.

Kellie Herbert, SLC6A1 Connect Symposium 2023

Erika Vanderberg, SLC6A1 Connect Symposium 2023

Kevin McEntee, Los Angeles SLC6A1 Connect Symposium 2024

Lindsay Randall, Los Angeles SLC6A1 Connect Symposium 2024

Everett’s mother, SLC6A1 Connect Symposium, Los Angeles 2024

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