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Have you heard of motor neurone disease (#MND)? It’s a disease that kills a third of people within a year, and more than half within two years of diagnosis. It kills six people a day. It has no cure. On #GlobalMNDAwarenessDay, put #MNDOverMatter and help us raise awareness!

Today is #GlobalMNDAwarenessDay & buildings across NI will be lighting up blue. Please send photos to [email protected]

Today is #MNDAwarenessDay and it's an opportunity for all of us to help to raise awareness of motor neuron disease. We've created this infographic to help educate people about MND - please share it as increasing awareness is vital 🤝 More about MND: myname5doddie.co.uk/about-mnd

“I put MND Over Matter by taking part in research for a future without motor neurone disease.” Dani is the fifth member of her family to have MND. She’s had over 70 lumbar punctures as part of a clinical trial to find a treatment for people with #MND. Dani is bravery

I am pleased to facilitate the lighting of Council buildings blue to raise awareness of Motor Neurone Disease #MNDAwareness Day is celebrated globally and aims to highlight the condition Full details: bit.ly/43MtrdE

Today is World ALS Day. As a part of the International Alliance of ALS/MND Associations, ALS TDI celebrates June 21st as the Global Day of Recognition of ALS/MND. Please help share to spread awareness of ALS/MND and the work being done to end this disease. #ALSMNDWithoutBorders

Big thanks to Yvette Cooper for speaking with people living with and affected by #MND at our event in Parliament today! #GlobalMNDAwarenessDay.

“I’m putting MND Over Matter by using my wheelchair to follow my passion for photography and help other people living with MND find accessible days out.” Ken struggled with his mental health following his diagnosis of #MND. The idea of being a full-time wheelchair user made

We had a fantastic awareness raising and fund raising event at Ulster University today for ゆう Marie Holmes on #GlobalMNDAwarenessDay. Special thanks to Ulster University Staff Disability Network, to the presenters, to everyone who attended and to all who have kindly donated to our Just-giving page Stephanie Duguez

“I’m putting MND Over Matter by sharing my story. If I can help just one newly diagnosed person feel less alone, then I’ve done my job.” Jennie is a mother-of-four and a PhD student. When she was diagnosed with #MND, very few around her knew what it was. She felt really lonely.

Newry Town Hall & Derry/Londonderry Council Offices lit up@in blue to mark #GlobalMNDAwarenessDay ⁦MNDA Northern Ireland⁩ ⁦MND Association⁩ #mndani

Yesterday, the skybridge on our Belfast campus was lit up for #GlobalMNDAwarenessDay. To all those battling with Motor Neurone Disease, you're not alone in this fight. Your strength and resilience inspire us all. 💙

Calling community organisations in the Northwest of Northern Ireland. Have your say on the training of new doctors in Derry-Londonderry. Check the details and contact us to participate.

The ALS/MND Alliance are looking to find out more about the experience of the global #MND #ALS community regarding fundamental rights. Have your say by taking part in the survey below ⬇

.Personalised Medicine Centre One week to our Personalised Medicine Centre 10th Anniversary Event. Really looking forward to this amazing showcase including speaker and poster sessions and guest speaker Liam Gallagher #10YearsOfResearchExcellence #BeMore #WeAreUU #ProudOfUU #1weektogo

On Duchenne awareness week - stories from 1 in 17 impacted by rare conditions

Fantastic talk from Dr Duguez and Dr Rene at the ALS and MND research meeting #ALS Stephanie Duguez School of Medicine | Ulster University ARSLA

New Cell Reports paper: Efficient exon skipping by base-editor-mediated abrogation of exonic splicing enhancers. tinyurl.com/4y6dyu4s

Bill's interview with Muscular Dystrophy UK. About his brother James, and his research career. School of Medicine | Ulster University Personalised Medicine Centre NIRDP Bill Duddy