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SMS Resources

Below we have provided links to resources providing information about Smith-Magenis Syndrome (SMS), living with SMS, SMS research and awareness tools.

Living with SMS

At the 2024 SMS Australia Camp, attendees were invited to build on the tips and tricks “What Works Wall” from the 2024 PRISMS conference, by contributing to our “Wisdom Wall” and sharing insights in our “Parents/Carers Tips & Tricks Roundtable” session.

We combined these inputs into a resource to help loved ones navigate their surroundings, participate in activities and enjoy life. These are meant to be helpful suggestions from family peers with lived experience and should not be considered fact-based research or medical advice. We ask you to please consult medical professionals or field experts before implementing any of these suggestions.

SMS Research

SMS Awareness

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