T
he PMG Awareness Organization is happy to announce this disease Patient Insights Network (PIN). We invite all polymicrogyria (PMG) patients and families to join this registry and to provide de-identified medical information that will help everyone in the global PMG community to learn more about the disease. The goal is improved diagnosis and medical care, as well as empowering patients and families with knowledge, connections and support.
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 the disease through education, research, advocacy, and support for individuals with polymicrogyria, their families, and other concerned parties.
T
he PMG Awareness Organization is happy to announce this disease Patient Insights Network (PIN). We invite all polymicrogyria (PMG) patients and families to join this registry and to provide de-identified medical information that will help everyone in the global PMG community to learn more about the disease. The goal is improved diagnosis and medical care, as well as empowering patients and families with knowledge, connections and support.
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