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The PMG Awareness Organization announces our own disease registry! We invite all Polymicrogyria (PMG) patients and families to join, to provide de-identified medical information to the registry to help everyone in the global Polymicrogyria community – patients, families, researchers, clinicians, and pharmaceutical companies – learn more about Polymicrogyria. The goal is improved diagnosis and medical care, as well as empowerment of patients and families through knowledge, connections, and support. 

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About Us

The PMG Awareness Organization is an international non-profit organization of families, caregivers, and medical professionals who care about those with Polymicrogyria. Our mission is to promote awareness, diagnosis, and the treatment of Polymicrogyria through education, research, advocacy, and support for individuals with Polymicrogyria, their families, and other concerned parties.