Information and Advice for Caregivers & Professionals
The Smith-Magenis Syndrome Foundation are very pleased to mark our SMS global awareness day by the release of our newly updated and formatted booklet ‘Information and Advice for Caregivers and Parents’. This can now be downloaded from our website by clicking here. We would like to thank Dr Lucy Wilde for all her dedicated hard work in researching, writing and creating this revised edition as well as all the members of the SMS professional board who provided input into the booklet. We hope you’ll agree that it is packed with useful information and has lots of practical advice for carers and parents raising a baby, child or adult with Smith-Magenis syndrome.