Smith-Magenis Syndrome is a rare condition that occurs one in every 15-25,000 births. People with SMS have complex needs and behaviours, along with a learning disability that can range from mild to profound. It is a lifelong condition that will always need extra support.

Our daughter Aurora was diagnosed with Smith-Magenis Syndrome last year at the age of 2. Without the SMS Foundation, we wouldn't have the support, information and advice that we do today and are forever grateful for this amazing charity. Please help support our cause for Aurora and others living with Smith Magenis Syndrome to lead a fulfilling life and help families struggling to live a normal life with this condition.