A year since the announcement of a review into the benefits system, more than 2,000 have died from MND, many struggling to access the benefits they desperately need. The review, announced in response
The MND Association has received a response to its open letter to the UK and Welsh Governments concerning unpaid carers. While the Welsh Government has provided some tangible proposals to better
More than 3081 supporters have signed an open letter calling on the Government to provide better support to unpaid MND carers during the COVID-19 pandemic. The letter will be sent to the Minister of
The All-Party Parliamentary Group (APPG) on MND hosted its first ever online meeting today to discuss the impact of COVID-19 on the MND community. The meeting was chaired by Andrew Lewer MBE MP,
Caring for a loved one with MND can take a physical and emotional toll, with some carers already struggling to cope and receiving very little support. Life is often hard for MND carers physically,
On 5 June 2020, the All-Party Parliamentary Group (APPG)* on MND is meeting online to discuss the impact of COVID-19 on people with MND, the MND Association and medical research into MND. The speakers
We want to thank each and every one of our supporters for their contribution to the #GetMNDonTheList campaign. Over the last few weeks, we have seen considerable media coverage on the issue, over 5200
The Motor Neurone Disease Association have secured support from their patron Academy Award winning actor Eddie Redmayne OBE and rugby heroes Doddie Weir OBE (Scotland, Newcastle Falcons) and Rob
The MND Association’s Scrap 6 Months campaign film is a finalist at the 2020 Charity Film Awards. ‘Jack and Rose’s Story’ a short film inspired by a true story, illustrates why our
The MND Association is extremely concerned to see that people with MND have not been included in the Government’s list of extremely vulnerable persons in their guidance on shielding and protecting