MND Matters Podcast
Created by the MND Association, the podcast will explore a wide range of subjects alongside people affected by MND. As well as being an extra information source for the MND…
When a Covid Christmas could be your last…
If you take away the extravagance of turkeys, tinsel and trees, Christmas is about community. Sharing love and gifts and moments of laughter. To connect with others is a primal…
An interview with Lynette Matravers on coping with lockdown as a carer for someone living with MND
“Brian’s not on the scrap heap. Just because he has Motor Neurone Disease, it doesn’t mean he can’t be helped”. Interview by Scarlett Parr Reid, Medical Communicator.…
Medical conditions won’t wait for the pandemic to pass. It’s time for the government to support medical research charities
‘When I got my diagnosis, I always tried to keep positive and say I would beat this. As I got sicker, I knew the only hope may be a…
Let’s Walk to D’Feet to raise awareness of the disease!
Each year, the 21 June is marked as MND Awareness Day and people from across the world are encouraged to share their stories, raise awareness of the disease and raise…
RAISING AWARENESS AT THE UNIVERSITY
We recently had the opportunity to have a stand at an event for medical students at Exeter University, to promote motor neuron disease, by informing students and welcoming any that…
ACT TO ADAPT – CAN YOU HELP?
The MND Association’s Act To Adapt campaign aims to raise awareness of the issues people with MND face in getting home adaptations and call on councils across England and Wales…