Forum rules, updates, and news on the work of the Association. Having trouble with the forum? Then post in here and let us know!

If you are new to the forum then why not introduce yourself here? Only include information which can be made public.

A place to discuss life with motor neurone disease. Learn from the experience of others and share your own tips.

We are sorry for your loss. Bereavement impacts us in unique ways and there are no right or wrong ways to grieve. In this forum you can share your experience with others experiencing, or who have experienced, grief and bereavement. This is a safe space in which to share your thoughts, concerns and maybe start to explore how to cope with your loss. We hope you find some of the help you need here.

You're not alone! Ask questions about motor neurone disease to our MND Connect team. Our team aim to answer as soon as possible. This group is covered 9 - 5 on weekdays. If you have a question, please post a new thread.

A place to talk about caring (or previously cared) for a partner, family member or friend with MND.

Not all member discussion here will be scientifically proven. At the present time, the only drug that has been proven to slow the progression of MND is Riluzole.

A place to discuss how you are getting involved with the Association whether its a campaign, fundraising, volunteering or something else. If you're in a branch or group why not share what you're up to too!

A place for those important questions about travelling, wheelchairs, accommodation and home adaptations, transport and choosing the right vehicle.

Discussion on all equipment and technology that you've found useful. From tablets, to software and apps, or items to help you with your daily living.

Help with everything financial, from Disability Living Allowance (DLA) and Personal Independence Payment (PIP), to benefits advice and our support grants.

An 'off topic' area to chat about non-MND issues, tell some jokes (keep it clean!) and have some fun and games.