Motor neurone disease (MND) is a fatal neurological condition
The MND Association:
- Funds research
- Supports patients carers and professionals and
- Campaigns for better care.
We have high quality information and resources for people with MND and their carers and families. This includes our comprehensive, award winning Carers Guide. The website area dedicated to carers can be found here.
Our young people’s hub, with information designed specifically for those aged 4-10 and 11- 18, can be found here.
Our MND Connect helpline is available Monday to Friday between 9am - 5pm and 7pm - 10:30pm. Call 0808 802 6262 or email email@example.com
We offer grants to help the main carer to take a break from their caring duties. This may be a pamper day, a short break or assistance towards pursuing a hobby and can be applied for up to 12 months post bereavement. We also offer a young person’s grant to help support purchases of anything that may help them in their day-to-day life eg, buying a laptop or going on a school trip. For information about all grants, click here.
We provide a range of local support including Association Visitors and a network of branches and groups. Information about our services can be found here.
We campaign and raise awareness so the needs of people with MND and everyone who cares for them are recognised and addressed by the wider society.
Nick Goldup, Director of Care Improvement says:
“Supporting carers is a huge priority for the MND Association as caring for someone with MND can be incredibly difficult due to the everchanging and complex needs of the disease. Our recent survey of MND carers revealed stark findings about carers’ struggle to access the support they deserve and the immense pressure they are under. This has fuelled our Support MND Carers campaign which launched at the end of 2022 and will take steps to address some of the key issues highlighted. We are proud to be part of Carers Week and collaborate with other organisations who are equally as passionate about support for unpaid carers.”