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AWARENESS      RESEARCH      SUPPORT

Mission

Promote awareness, stimulate research, and support families affected by WAGR syndrome

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Vision

To be the world's most respected source of help, hope, and information for those touched by WAGR syndrome

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Values

Respect and compassion.  Ethics, trust, and transparency.  Stewardship and fiscal responsibility.  Commitment to learning, collaboration, innovation, research, and privacy.  Membership and access to information and support will always remain free

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Stakeholders

Individuals with WAGR syndrome, families, friends, and caregivers; physicians and medical professionals; researchers; therapists; teachers; rare disease and nonprofit organizations; and aniridia patients and organizations

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