The Motor Neurone Disease Association (MNDA) is a membership organisation which aims to improve access to care and research, as well as campaigning, for those people living with or affected by MND.The MNDA currently has over 10,000 members and more than 7,000 volunteers, forming a national and local network that provides information and support to those affected and their relatives and carers.MND affects up to 5,000 adults in the UK at any one time, and one of the Association’s main aims is to raise awareness and understanding of motor neurone disease.Although not a form of motor neurone disease, the MND Association also offers support to people with Kennedy’s disease, a rare disorder of the motor neurones also known as spinal bulbar muscular atrophy (SBMA), caused by a genetic mutation.The MND Connect team offers information and support on all aspects of motor neurone disease. This service is available for:people living with MND,carers,family members,health and social care professionals,MND Association staff and volunteers,or anyone else affected by MND.and can provide:information about MND,emotional and practical support,social, practical and financial information,information about local support,information about how the MND Association can support yousignposting to other appropriate services.MND Connect is available from Monday to Friday, between 9am and 4pm. Calls to this number are free from landlines and mobile phones within the UK and are confidential.For more information, please follow the link to the MNDA website, or contact using the details provided. We're sorry but <%= htmlWebpackPlugin.options.title %> doesn't work properly without JavaScript enabled. Please enable it to continue.
