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Congratulations and well done to Barts Health who have recruited their first patient to COMMEND Project! Thank you to the local site team!

Abstracts for the 29th International Symposium on ALS/MND are now available to view online. This includes abstracts of 109 talks and over 400 poster presentations that will be presented at this year's #alssymp in Glasgow, in just over two weeks. mndassociation.org/symposium/abst…

Huge congratulations to #Scottish #rugby hero and MND Association supporter #DoddieWeir (seen here with MND Research director Brian Dickie) on his #OBE for services to #MND research 🏅 #NewYearHonours

Another fantastic opportunity to share the DiAMoND Study with an important audience. Great support for our work and thought provoking discussions 💡 #MND #shareddecisionmaking #feedingoptions

People affected by MND are at the heart of everything we do here at KingsMND. We need your input to tailor our services and future research. If you're interested in helping us do this, you can join our advisory group. DM us for details and our coordinator will email you back #MND

Calling #MND clinicians: please take 10mins to fill DWP’s survey on reforming the welfare benefits system for terminally ill people. Give your views on the process before 29th Feb bit.ly/2wpGln5

So far we have NIV-4-MND Better NIV for MND

Celebrating Dr Guillaume Hautbergue, who has been elected as a Fellow of the Royal Society of Biology in recognition of his “prominent contribution to the advancement of the biological sciences” as a Senior Lecturer in Translational RNA Biology.

I've emailed my MP to ensure motor neurone disease is added to the list of 'extremely vulnerable persons' as a matter of urgency. Help protect people with #MND from #coronavirus #Covid19 by emailing your MP too. ecampaigns.mndassociation.org/page/58148/act…

It would be great to capture thoughts of participants in MND studies in this NIHR survey...

Thank you @SteveBakerHW for your crucial support in the fight against #MND. With dedicated funding we can build on recent advances in our understanding of MND and make this disease treatable. #United2EndMND

Over the next 5 years we want GOV.UK to invest £50 million into motor neurone disease (#MND) research. You can help us. We're #United2EndMND. Please add your name to our petition 👇 petition.parliament.uk/petitions/5645…

The ALS Biomarkers study has been updated to allow people to provide biosamples using simple at-home collection kits, allowing patients to take part regardless of where in the UK they live. The study is recruiting patients with MND & healthy individuals mndcsg.org.uk/mnd-clinical-r…

#Clinicalresearch supported by AMRC charity MND Association has helped improve quality of life for people with motor neurone disease. Find out more in our #MakingADifference impact report: bit.ly/3fe1XW7. #charityimpact #CTD2021

MND patients, carers, family members - Can you help researchers understand patients & carers priorities? Would you be interested in joining a vibrant group of lay advisors supporting Sheffield researchers to develop new research proposals? smndrag.group.shef.ac.uk/2021/05/new-me…

Please take a few moments to pause and reflect on this inspiring and motivating open letter to MND researchers from a patient living with MND. mndcsg.org.uk/2021/06/open-l…

BREAKING 🥳 WE DID IT! The GOV.UK has now agreed to commit £50 million to fund specific research in to motor neurone disease in response to our #United2EndMND campaign. It's made the front page of Sunday's Daily Express, which has supported our fight 🔬 express.co.uk

Researchers in Sheffield are aiming to understand how to better support people with MND making the complex decision to have a gastrostomy placed. If you are a HCP in the UK who has been involved in these discussions, please consider completing the survey shef.qualtrics.com/jfe/form/SV_4N…