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The Motor Neurone Disease Association is an excellent source of information. They also have a helpline that people can phone at any time and it has information for patients with motor neurone disease, all about the condition. There are videos, there are learning resources for professionals and the MNDA, importantly, can support patients with financial support as well, which is an excellent provision. They also train up volunteers. We have local volunteers that will see patients at home and support them, and they will often have little branch meetings and organize outings. And our local group are very active and even have produced a recent newsletter.
