The EIP's Think Rare Program empowers pediatricians and general practitioners (GPs) to identify rare and underdiagnosed conditions early. By considering "rare diseases" in your everyday practice from the initial signs, you can transform a child’s life—enhancing outcomes, enabling early intervention, and offering hope to families.
Each zone focuses on a specific rare disease, equipping you with condition-specific knowledge, signs to watch for, patient stories, and up-to-date resources.
Learn to spot the early signs of this progressive metabolic disorder and prevent delays in diagnosis.
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Recognize cognitive and motor regression early — before symptoms are mistaken for other conditions.
A digital library of past conferences and educational sessions available anytime.
Our faculty is composed of international experts, clinicians, and researchers dedicated to transforming the way rare diseases are recognized and managed at the primary care level.
The Think Rare Program is made possible through the support of organizations, institutions, and industry partners who share our vision of early recognition and better outcomes for children with rare diseases.
