MND EnCouRage UK is back and the whole MND community is invited!
— Hear about the latest MND research
— Engage with researchers
— Take part in discussions about research
Spaces are limited!
Register your interest by 8th June ⬇
https://t.co/QKffm6rvB6
#MNDEnCouRageUK
Project Manager role with the MND Association leading research system delivery, procurement, supplier management and change support for grant funding processes. Closing date: 15th June
https://t.co/EWl34olnsy
The Patient Fellows Program aims to bridge the gap between people with MND, carers, gene carriers and researchers.
If you are interested in research, the Program can help you attend the International Symposium on ALS/MND, the largest international conference dedicated to ALS/MND research 🌍
Learn more: https://t.co/LnWEbjb9ty
#MND #ALS #alsmndsymp
🚨 Calling all researchers! There's only 1 week left to submit your application for our Advancing Treatments Award. We want to fund projects that will further the early-stage development of new treatments to slow, stop or reverse MND progression
Details: https://t.co/xKMhzfYjKH
It’s Volunteers’ Week!
A huge thank you to everyone who volunteers for MND research.
Your commitment is helping to drive better care and bringing us closer to effective treatments for everyone with MND.
We couldn’t do this without you 🧡
#MND#VolunteersWeek
Poster sessions at the International Symposium on ALS/MND are the perfect way to showcase your research to the wider community!
Submit your abstract to have the opportunity to present at the poster sessions in Amsterdam in December.
Deadline: 9 July
More: https://t.co/0OTzEHvgBc
#alsmndsymp
Are you an early career researcher working in MND in the UK?
Why not apply for the @mndassoc Rob Burrow Early Career Researcher Prize?
Find out more and apply⬇️
https://t.co/PBtNz53zsM
📢 Last Call for Abstracts: April 28 – June 1. Time is running out to share your work with the global ALS/MND community in Amsterdam - submissions for the Allied Professionals Forum, Alliance Meeting, and Poster Hall.
📅 Deadline: June 1, 2026.
➡️ https://t.co/Bcjv52cBRb
Why is MND EnCouRage UK important?
It brings together the MND community, opening up new conversations and collaborations.
It provides an opportunity for people affected by MND to learn more about research minus all the scientific jargon!
Register your interest to attend ⬇️
https://t.co/aa0XxYAOYE
Some people with MND also develop frontotemporal dementia (FTD).
Dr Alex Thompson @MNDOxford is looking at toxic protein clumps found in MND and FTD to understand how these spread through brain cells and contribute to disease progression.
Find out more: https://t.co/vmAUlZfNzy
#DementiaActionWeek #FTD #MND
MND EnCouRage UK is a unique event where people with MND, families and carers can hear the latest research.
You’ll meet early career researchers, join small‑group discussions, and share your lived experience to help shape future MND research. Community registration is now open for the 15 July event in Loughborough.
🔗https://t.co/WKysE2KNR0
Looking to find out more about MND clinical trials?
Head over to our website to find out:
— where they are recruiting
— what the drug is thought to do in the body
— latest updates from the trial
Find out more today: https://t.co/BWFGfWBsLP
Want to find out more about MND clinical trials in 2026?
Our blogs cover updates to look out for this year!
Head over to our blog to find out more: https://t.co/wiAG9OfXpK
#ClinicalTrialsDay#MND
What is a clinical trial — and why are they essential for finding new treatments for MND?
Our back to basics blog breaks it all down 👇
https://t.co/dGwb056ilS
#ClinicalTrialsDay#MND
On Clinical Trials Day, we’re saying thank you to everyone behind MND clinical trials — especially those with MND, their families and carers, and the healthcare professionals who support them.
Your commitment makes a real difference 🧡
#ClinicalTrialsDay#MND
📢 Call for Abstracts Open: April 28 – June 1. Big ideas. Real impact. Global reach.
We’re now accepting submissions for the Allied Professionals Forum, Alliance Meeting, and Poster Hall.
📅 Submit by June 1, 2026.
➡️ https://t.co/Bcjv52cBRb
We’ve launched a bold new five‑year research strategy shaped directly by people with MND — and their hope for a future free from the disease.
To get there, we’re backing the brightest early career researchers, expanding funding, training and real‑world insight, and opening new doors for data scientists to accelerate breakthroughs. From EnCouRage UK to the Rob Burrow ECR Prize, we’re building the next generation of leaders who will help defeat MND.
Read more about our commitment to supporting career researchers in this blog by our Director of Research and Innovation, Mike Rogers:
🔗https://t.co/cMLprDRVyP
Did you know?
Changes in a gene called C9orf72 are linked to the development of MND and a form of dementia called frontotemporal dementia (FTD).
Around 15% of people with C9orf72-MND experience FTD.
#DementiaActionWeek#FTD#MND
ICYMI- Want to hear about some of the cutting-edge MND research happening in the UK?
Join us at MND EnCouRage UK!
— Engage with researchers
— Take part in discussions about research
Spaces are limited!
Register your interest by 08 June ⬇
https://t.co/aa0XxYAh96
#MNDEnCouRageUK