- On the back of accelerating access to £50 million for motor neurone disease (MND) research, Health and Social Care Secretary hosts roundtable with researchers, charities and patients to speed up progress in developing treatments
- The roundtable identified how leading researchers, scientists and the government can work better together to fast-track finding a cure
- Everyone in England can now sign up to research into MND and other conditions via the NHS App.
People with motor neurone disease (MND) are set to benefit from improved collaboration between the government, researchers and charities, on top of accelerated access to funding, to speed up progress into developing treatments and finding a cure.
The Health and Social Care Secretary Steve Barclay met with leading representatives from across the MND research community yesterday, including medical research charity LifeArc's Dr Catriona Crombie, MND charities Name'5 Doddie Foundation, MND Association, and MND Scotland, and patients, to discuss ways to fast-track research into the disease and look at how the government and sector can work better together to benefit patients.
MND continues to have a devastating impact on the lives of people living with the condition and their families. The roundtable set out how the government will continue to work closely with the research sector, cut red tape to make accessing funding easier and boost research into new treatments.
Following the roundtable, the Health and Social Care Secretary visited the King's College Hospital MND Care and Research Centre - which was the first in the country and is now one of 22 research centres - to meet staff, patients and charities to see first-hand how government funding for MND research has benefitted them. King's research labs helped find the only current treatment that targets the underlying causes of neurological diseases such as MND, and is aiming to find a cure and improve quality of life for patients and their families.
The NHS App has also now been updated to make it easier for people to take part in MND and wider health research. People will be able to visit Be Part of Research through the app to view and sign up to research.
Health and Social Care Secretary Steve Barclay said:
Motor neurone disease can have a devastating impact on people's lives, and I'm working with leading researchers to accelerate research and help find a cure as soon as we can.
We have made strong progress since we pledged £50 million for MND research with new treatments being developed and promising results from clinical trials reported, but I know there is still more to do. Yesterday, I held a roundtable with experts, charities and patients to discuss how we can encourage and invest in the best research to drive more results.
By cutting red tape and building on existing investments, we are making sure funding gets to researchers as quickly as possible. I encourage people in England to sign up to research via the NHS App and join our ever-growing UK-wide register Be Part of Research.
There are many different types of research users of the NHS App can sign up to, including studies that test new treatments via interviews or surveys. A study might take place in a hospital, GP practice, or other health and social care locations in the community but some studies can also be done at home, online or by telephone.
For example, dentist and former football manager Dean Mooney, whose life has changed dramatically since his Amyotrophic Lateral Sclerosis (ALS) diagnosis, has appealed to others who have the disease to join him in a new brain imaging study to help the race to find new treatments. Dean has worked with the University of Exeter's world-leading Neurodegeneration Imaging Group, led by Professor Marios Politis, that is appealing for people who have MND to
