The Smith-Magenis Syndrome (SMS) Foundation UK shall be at the heart of our community of individuals, families, carers and professionals living and working with Smith-Magenis Syndrome and we will be the first point of contact for those seeking information and support. Nobody living with SMS should ever feel isolated or alone. Through our conferences and events, online presence and social media platforms we will connect families, raise awareness and build futures.
Contact detailsPhone number:
0300 101 0034