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The issues in the world can feel huge at the moment. But community brings so many of us together. My 18 year old son with Smith Magenis Syndrome was so happy to be picked from the audience to dance with the Pacifika group at FluroFest yesterday. Well done to Erika Harvey and her team for bringing community to Tauranga. Thank you to the young dancers for making his day!
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As we close out the year, we are reminded of the extraordinary strength of the Smith Magenis Syndrome community, families, advocates, and donors united by hope and determination. Because of your support, the SMS Research Foundation is funding groundbreaking research at McGill University and Stanford University, pushing the field closer than ever toward potential treatments for SMS. This work is part of several critical efforts accelerating progress at a moment when scientific advances are making
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