This special episode takes a look back at the journey of understanding Williams syndrome—and how the WSA has grown alongside it. Through past interviews, we hear from leading voices in the field: Dr. Barbara Pober, Dr. Marty Levinson, Dr. Elizabeth Barnhardt, Dr. Becca Lyren, Dr. Jocelyn Krebs, Dr. Ben Jacob, and former WSA Executive Director Terry Monkaba.
Together, their insights paint a picture of how research, diagnosis, care, and community support have evolved over time. Whether you're new to the WS world or have been walking this path for years, this episode connects the dots between where we started—and where we're headed.
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