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CLS Talks: Partnering for Progress in Neurodevelopmental Disorders

February 2026 (Time TBD)

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Zoom

Learn how parents and researchers are working together to advance care and understanding of X-linked neurodevelopmental disorders.

CLS Talks: Partnering for Progress in Neurodevelopmental Disorders
CLS Talks: Partnering for Progress in Neurodevelopmental Disorders

Time & Location

February 2026 (Time TBD)

Zoom

About the event

The Coffin-Lowry Syndrome (CLS) Foundation hosts CLS Talks, a quarterly interactive Zoom series created by parents, for parents. Each session explores topics that matter most to families in the rare disease community.


In the upcoming session, Dr. Jin Lee, founder of CURE NDD, will discuss the consortium’s mission to advance research, advocacy, and awareness for neurodevelopmental disorders — with a special focus on X-linked conditions. The CLS Foundation is a proud member of the CURE NDD Consortium.


📅 When: February 2026 (Time TBD)

💻 Where: Zoom

📩 To Attend: Contact CLSFoundation@outlook.com. Members of the CLS Foundation Facebook group will automatically receive an invitation.

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Every day counts for children and families affected by X-linked neurodevelopmental disorders.

Cure NDD, a 501(c)(3) nonprofit, is working to fast-track research and therapies where options are limited or nonexistent.

Your tax-deductible donation directly supports the path to cures.

EIN: 39-5006055

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