admin – Page 2 – Project 8p – Creating a path to treatment for chromosome 8p disorders through research, community, and intelligent information

REGISTRY ENROLL

Understanding Telehealth Services as a Parent of Special Needs Children

Commission on Novel Technologies for Neurodevelopmental CNVs

Chan Zuckerberg Initiative to fund 30 patient groups, aiming to build a model for tackling rare diseases

Travel Tips for Parents with Special Needs

National Music Month: Music Therapy and 8p Heroes

Project 8p Member on BBC Radio Scotland

Project 8p Interview on Ovid Therapeutics’s Bold Medicine Podcast

Weatherford Democrat – Weatherford family hopes to travel to NY for rare disorder conference

New Zealand Herald – Kathryn Hazeldine: The life of a 5-year-old with chromosome 8p condition unable to yet walk or talk

Bravo TV – Denise Richards Breaks Down While Explaining the Rare Disorder That Affects Her Daughter, Eloise

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