Cure DM is dedicated to providing support to those living with Myotonic Dystrophy, their families and caregivers. We do this by organising an anual 'Families Day' get-together in July each year, as well as smaller mid year events, such as trips to 'Disney on Ice'... We facilitate research into DM, and are deeply involved from clinical trial design to representing the DM community to the regulators. We support and fund research in many forms, and publish up to date medical and treatment pipelines, ensuring accurate and up to date infomration reaches the community! We are also passionate about raising awareness, within the cientific and medical community via infomration sheets, posters and guidelines, and also to the community and public. We are extremely proud of the part we played in organising the annual DM Awareneness day, which is a worldwide campaign on September 15th each year. None of this would be possible without your support, so THANK YOU!