||The Alzheimer's Society is the UK's leading care and research charity for people with any form of dementia and their carers.
||Ataxia UK helps people affected by ataxia with research, information, contacts, a helpline, and grants to members in need.
||The Ataxia-Telangiectasia Society is working to improve the quality of life for children and adults with Ataxia-Telangiectasia ("A-T") and their families through research, support and awareness.
||The British Acoustic Neuroma Association is a patient organised and administered information and mutual aid group, which exists for mutual support, information exchange and mutual listening.
|Brain and Spine Foundation
||The Brain and Spine Foundation was set up in 1992 to develop research, education and information programmes aimed at improving the prevention, treatment and care of people affected by disorders of the brain and spine and to stimulate the greater allocation of resources across all neurological disorders. The Foundation has produced many booklets on a variety of neurological conditions, work books for schools and colleges, and educational videos for GPs and other health professionals.
|Brain & spinal injuries
||Since 1986 the Brain and Spinal Injury Charity has been raising funding for research into the brain and more recently they have extended their services to include support and information for those recovering from these conditions.
||The UKABIF is a not-for-profit coalition of organisations and individuals that seeks to promote understanding of all aspects of acquired brain injury and to provide information and expert input to policy makers and others to promote the interests of brain injured people and their families.
||Scope is a disability organisation in England and Wales whose focus is people with cerebral palsy.
|Child brain Injuries
||The Child Brain Injury Trust aims to improve the quality of life for all children and young people who have an acquired brain injury and to enable them to achieve their full potential.
||Charcot-Marie-Tooth UK works to support those who are affected by Charcot-Marie-Tooth Disease, also known as Hereditary Motor and Sensory Neuropathy or Peroneal Muscular Atrophy
|National Creutzfeldt-Jakob Disease Surveillance Unit CJD
||The incidence of Creutzfeldt-Jakob disease (CJD) is monitored in the UK by the CJD Surveillance Unit based at the Western General Hospital in Edinburgh, Scotland. The unit brings together a team of clinical neurologists, neuropathologists and scientists specialising in the investigation of this disease.
The CJD Support Network is a patient support group providing help and support for people with all strains of Creutzfeldt-Jakob disease, their carers and concerned professionals.
It also provides support for people who have been informed that they are at a higher risk of CJD through secondary transmission i.e. blood transfusion or surgical instruments.
||Ouch (UK) provides support for sufferers of cluster headaches and their families, and to increase public awareness of the condition.
||The mission of For Dementia is to improve the quality of life for people affected by dementia.
||Speakability is the national charity that supports people living with aphasia and their carers through its information service, national network of groups and activities programme; influences individuals, organisations and statutory bodies in order to improve services for people living with aphasia; and raises funds to support these aims.
||The Dystonia Society is a medical charity, established in 1983, working for the benefit of all who suffer from dystonia and those who care for them.
||The Encephalitis Society provides information and support to improve the quality of life of all people affected directly and indirectly by encephalitis.
||The National Society for Epilepsy is striving for a world without epilepsy. In the meantime we will seek to enhance the Quality of Life of people affected by epilepsy by promoting research, education and public awareness, and by providing specialist medical care and support services.
||Epilepsy Action provides information about coping with epilepsy and seizures including help and advice through the use of email and Freephone telephone helplines.
||The GBS Support Group provide information and support to those suffering from Guillain-Barré syndrome and related neuropathies including CIDP and Miller Fisher syndrome.
||Head Injury Re-Education is an organisation dedicated to helping children, young people and adults who have acquired brain injury and whose lives has been affected as a result.
||The aim of Headway is to promote understanding of all aspects of brain injury; and to provide information, support and services to people with a brain injury, their family and carers.
||Hemihelp aims to offer information and support to families where there is a child with hemiplegia and raise awareness about the condition amongst both the professionals who work with our children and the public.
||The Huntington's Disease Association exists to support people affected by the disease and to provided information and advice to professionals whose task it is to support Huntington's disease families.
||The Meningitis Trust produces information to raise awareness of the disease, funds research into vaccines and treatment, and offers a wide range of support for people affected by meningitis and meningococcal septicaemia.
||The Migraine Trust is committed to supporting sufferers and their families by funding and promoting research, improving diagnosis and treatment, providing information and advice, and raising awareness of migraine as a significant public health problem.
||The Migraine Action Association (formerly the British Migraine Association) aims to bridge the gap between the migraine sufferer and the medical world by providing information on all aspects of the condition and its management.
|Motor neurone disease
||The Motor Neurone Disease Assoication is the only national organisation in England, Wales and Northern Ireland dedicated to the support of people with MND and those who care for them.
||The MS Society is the main source of reliable information about MS and the leading UK funder of MS research while also providing a strong voice on issues related to MS. Its nation-wide network of branches provides information and support to everyone affected by MS.
Cheltenham Branch: www.mssociety.org.uk/cheltenham
||The MS Trust is a charity for people with multiple sclerosis, their families and friends, and for all health professionals who work with them. Information offered about MS, education for nurses and other health professionals and fund applied research.
|MS Active Source
||MS Active Source is a web-based society built for the MS Community in the UK and Ireland. The site aims to address needs and has been built incorporating feedback from MS websites, people with MS and MS nurses. It gives links to information and MS support groups.
|Multiple system atrophy
||The Sarah Matheson Trust (SMT) is the recognised United Kingdom support and information service for people with Multiple System Atrophy (MSA), their families and carers.
A local support group is also available. Contact Janice Davies 01242-224617.
||The Muscular Dystrophy Campaign is the only UK charity focusing on all muscular dystrophies and allied disorders.
||The Myasthenia Gravis Association (MGA) has as its objective the promotion of the welfare of sufferers from Mysathenia Gravis in the United Kingdom and the Republic of Ireland.
||Narcolepsy Association UK (UKAN) is an association of narcoleptics, their relatives and others for the benefit, relief and aid of persons suffering from narcolepsy.
||The Neurofibromatosis Association aims to fight neurofibromatosis by acting as a mutual support group, linking those affected to each other and with the medical profession, providing information, and raising funds to support research.
The Neurological Alliance enables charities to work together to improve the quality of life of all those in the UK living with a neurological condition. It offers links to neurological charities and publications.
||Pain Concern offers information and support for pain sufferers, with free Factsheets and leaflets to help manage pain, a quarterly magazine, updates on the latest developments, and a listening-ear helpline.
||The aim of the Parkinson's UK is the conquest of Parkinson's disease and the alleviation of the distress it causes through research, education, welfare and communication.
||The Cure Parkinson's Trust is a patient-led charity dedicated to finding a cure for PD.
||The Pick's Disease Support Group tries to decrease the burden by providing information and support to those caring for people with fronto-temporal dementia. The group includes:1. Dementia with Lewy Bodies 2. Frontotemporal Dementia including Frontal Lobe Degeneration, Pick's Disease and Primary Progressive Aphasia 3. Alcohol Related Dementia 4. Corticobasal Degeneration
||The British Polio Fellowship (BPF) is a registered charity that provides information and advice about rights, housing issues, equipment, self-management courses, and the late effects of polio/post polio syndrome.
|Progressive Supranuclear Palsy
||The PSP Association was set up in 1994 by a family afflicted with PSP to provide information and support to sufferers and their carers across Europe, to promote and sponsor research worldwide and to engender awareness of this disease and the Association, mainly within the UK.
||The Rett Syndrome Association UK is a national organisation giving help, advice and support to parents, carers, siblings and professionals - in fact anybody - involved with a child or adult who has Rett syndrome.
||Moving Forward helps people with spasticity by publishing information that can lead to a better understanding of this condition, improved treatment, and quality of life. The Association also supports health professionals that want to learn more about the most up-to-date and effective management techniques and treatment.
|Spina bifida & hydrocephalus
||ASBAH aims to improve services for people with spina bifida and/or hydrocephalus, to work with them to extend their choices, and maximise opportunities for independence and achievement.
|Spinal Injuries Association
||SIA is the national organisation of spinal cord injured people. We represent all their interests regardless of how the impairment occurred, whether or not it has resulted in full or partial paralysis. We support all those who are affected by spinal cord injury, including the family and friends of the disabled person.
|Spinal Muscular Atrophy
||The Jennifer Trust for Spinal Muscular Atrophy is the only national charity in the UK dedicated both to supporting people affected by SMA and investing in essential research.
||The Stroke Association provides support for people who have had strokes, their families and carers. They campaign, educate and inform to increase knowledge of stroke at all levels of society.
||Different Strokes is a charity set up by younger stroke survivors for younger stroke survivors.
||Ann's Neurological Trust Society facilitates self help and support for sufferers and carers from syringomyelia and related conditions.
||The Tourette Syndrome (UK) Association is a registered charity dedicated to providing support, educating, informing and campaigning, and promoting medical research on behalf of all those affected by TS.
||The National Tremor Foundation aims to offer a support and advice service to people of all ages who have been diagnosed with tremor of all types.
||The International Essential Tremor Foundation is devoted to helping people with essential tremor, the commonest form of tremor.
||The Tuberous Sclerosis Association supports sufferers, promotes awareness, and seeks the causes and best possible management of Tuberous Sclerosis. All aspects of the Association's work are aimed at improving the quality of life of those who are affected by Tuberous Sclerosis.