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MND Association has developed a number of Care Centres and Networks across England Wales and Northern Ireland.
We improve care and support for people with MND, their families and carers.
We fund and promote research that leads to new understanding and treatments, and brings us closer to a cure for MND.
We campaign and raise awareness so the needs of people with MND and everyone who cares for them are recognised and addressed by wider society.
People with MND, their families and carers are at the heart of everything we do. We collaborate, and value everyone’s contribution.
We achieve excellence through personal commitment and ongoing improvement.
We respect and respond to people’s diverse needs, backgrounds and views.
We achieve our aims through building open and transparent relationships.
Contact: West London Branch of Motor Neurone Disease Association
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MND Association has developed a number of Care Centres and Networks across England Wales and Northern Ireland.
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Do you know someone with motor neurone disease (MND)? If you are aged up to 18, find out more here. There is also information for parents and guardians, including professionals who may be giving support.
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We help people with MND experiencing speech or communication difficulties, or if you want to prepare for the potential need for assistance in the future. This might include the use of communication aids, computer access systems, or using technology to create a synthetic version of your own voice.
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We loan equipment to individuals with Motor Neurone Disease.
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The Motor Neurone Disease (MND) Association is able to offer some financial support.
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The MND Connect team offers information and support on all aspects of motor neurone disease (MND), including symptom control, practical management, improving quality of life, clinical research and signposting to other organisations.
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As a carer of someone with MND, you can access help from care services as care needs increase.
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