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PRISMS is dedicated to providing information and support to families of persons with Smith-Magenis Syndrome (SMS) and fostering partnerships with professionals to increase awareness and understanding of SMS.
PRISMS serves as a central clearinghouse for information about SMS, providing a range of educational and support services, including telephone support; database of registered families; official newsletter – Spectrum; information packet, brochures for families, caregivers & medical professionals; Parent-to-Parent Program; and an International conferences on SMS