Every day we drive research into motor neurone disease — from understanding causes to finding treatments. Because every day matters.

England, Wales & N. Ireland
ICYMI- Abstract submission is now open! Submit your abstract to present your research at the 37th International Symposium on ALS/MND! — 9 – 11 December 2026 — Amsterdam, the Netherlands (+ virtual) Find out more: symposium.mndassociation.org… #alsmndsymp
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Are you watching #corrie tonight? In the special episode we follow Paul and Billy and highlight the challenges people with #MND #ALS face. A big thank you to @itvcorrie for helping raise awareness of motor neurone disease. 💙🧡 nitter.app/Dan_Brocklebank/status…
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Wow. #MNDEnCouRageUK was incredible. We are incredibly proud of the early career researchers who got stuck in, took feedback on board and gave brilliant talks. Thanks to the #MND #ALS community for spending time with us and reinforcing why research matters. See you next year! 👋
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To create a world free of #MND/#ALS, we first need to find effective treatments. 🔬 EXPERTS-ALS, supported by @mndassoc, aims to rapidly screen potential treatments and prioritise the most promising candidates. Read about the exciting research we fund: mndassociation.org/research/…
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⁉️ Are you still following us?? ⁉️ A little reminder that you may not following us any more. As part of @mndassoc we share the latest #MND #ALS research from all over the world, as well as details about the research your support funds. 🔬 Follow us to stay up to date!
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The development of tofersen for the treatment for #SOD1 #MND #ALS has brought genetic MND to centre stage. 🧬 At #MNDEnCouRageUK Prof Martin Turner gave an overview of the genetics around MND. He mentioned the importance of having the choice of genetic testing and counselling.
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✨ We’re back! ✨ You may have noticed we went quiet for a couple of weeks. But we are back posting about the latest and most exciting #MND #ALS research. 🔬 You also may notice that you’re no longer following us, please check so you continue to get the latest updates!
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.@AmmarAlChalabi is giving us a quick lesson on how our DNA makes proteins, which play a vital role in keeping our cells working and healthy! 🧬 Changes in DNA can happen in #MND #ALS and lead to faulty and toxic proteins. Gene therapies, like #tofersen, aim to correct these changes. #MNDEnCouRageUK
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#Researcherspotlight 💡 Dr Tobias Moll from @neuroshef is investigating how communication breaks down in motor neurons in #MND #ALS. He aims to test a new potential treatment strategy and hopefully reduce damage to nerve cells. More info: mndassociation.org/research/…
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#ResearcherSpotlight💡 Dr Puja Mehta joined us today at our virtual legacy event to discuss her research. 🔬 @DrPujaM is developing a new gene therapy which could be beneficial for around 97% of people with #MND #ALS. Find out more about her research⬇️ mndassociation.org/research/…
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𝐑𝐞𝐜𝐨𝐫𝐝 𝐛𝐫𝐞𝐚𝐤𝐢𝐧𝐠 We are thrilled to announce that we have had a record-breaking number of abstracts submitted to the 35th International Symposium on #ALS/#MND. 🙌 We can’t wait to hear about the most promising and cutting-edge research later this year. #alsmndsymp
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In the last 10 years @mndassoc research portfolio has almost trebled to over £21 million. A key part of our portfolio is translational research – which seeks to bridge the gap between lab research and clinical trials. Find out more in our new report ⬇️ mndassociation.org/research/…
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Closing this years #MNDEnCouRageUK is @PaulPdwright27 from @lifearc1. Paul discussed the importance of including people affected by the disease in the development of new treatments. A massive thank you to LifeArc for sponsoring MND EnCouRage. 💙🧡
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“Keep at it!” It was an absolute honour to hear Martyn (@mbarrow1) and Anna’s (@anbar1) story, after Anna was diagnosed with #MND #ALS. Raw, emotional and inspiring. Thank you for sharing with us and the early career researchers to highlight why it is so important to keep at the fight against MND.
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#ResearcherSpotlight 💡 @AhmadAlKhleifat is investigating if #AI can be used to help find subgroups of people with #MND #ALS who have similar biological pathways. This could lead to a more personalised approach to treating the disease. More info ⬇️ mndassociation.org/research/…
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Developing the next generation of researchers is vital in the fight against #MND #ALS. 🧑‍🔬 They may hold the cure in their hands, they just don’t know it yet. Watch below to find out how #MNDEnCouRageUK supports future research leaders and brings the community together ⬇️
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#MNDEnCouRageUK 2024 is underway!! This event is all about encouraging the next generation of #MND #ALS researchers. 🧑‍🔬 The future looks bright! ✨
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“I am committed to finding effective treatments for MND and FTD.” @RubikaBalendra won the 2024 #ENCALS Young Investigator award earlier this year, and chats about her #MND #ALS #FTD research in our latest blog post. Read more ⬇️ mndresearch.blog/2024/08/08/…
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A massive thank you to all of the presenters who helped make #MNDEnCouRageUK so incredible. 👏 @SimonHallNews @VPResearch_ALS @KristianaSalmon @ScottAllen38 @J9Kirby @AmmarAlChalabi @DrCarolineVance @PaulPdwright27 @lifearc1 @mbarrow1 @anbar1 Kevin Talbot, Martin Turner, Jackie Mitchell, Rob Layfield
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This afternoon we have been joined by the whole #MND #ALS community. We’re kicking off with the lightning talks. ⚡️ The early career researchers are sharing their #MND #ALS researcher in an understandable and engaging way. #MNDEnCouRageUK
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On day 1 of #MNDEnCouRageUK we: 🧑‍🏫 learnt how to communicate research effectively 👂 heard about the impact of an #MND #ALS diagnosis 🧑‍💼 took time to think about careers and progression. We can't wait for day 2, where we will be joined by people affected by MND. See you then!
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❓ Why is it so important to develop the next generation of #MND #ALS researchers? 🙋 One of them may hold the key to defeating MND Read about how the @mndassoc are supporting the future research leaders ⬇️ mndresearch.blog/2024/07/18/… #MNDEnCouRageUK #FutureLeaders
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#ResearcherSpotlight💡 @SarahGornall321 is investigating whether small changes in a combination of several genes can lead to the development of #MND #ALS. 🧬 Learning more about genetics in MND could lead to new potential therapies. Read more: mndassociation.org/research/…
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Developing the next generation of researchers is vital in the fight against #MND #ALS. 👨‍🔬 They may hold the cure in their hands, but they just don’t know it yet. Next week we are holding #MNDEnCouRageUK to encourage, train and support the future MND research leaders. Watch below to hear what delegates thought of last year's event! ⬇️ #ResearchAppreciationDay
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To find effective treatments and make a difference for people living with #MND we need talented researchers. 👩‍🔬👨‍🔬 #MNDEnCouRageUK aims to develop the future leaders of MND research. Joining us? Start creating new connections by sharing that your attending!
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#MND #ALS researchers are working together more than ever. 🧑‍🔬 One focus is searching for new and better ways to carry out clinical trials, to find effective treatments quicker. Find out how @mndassoc are supporting researchers ⬇️ mndassociation.org/research/…
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Award winning researcher @RubikaBalendra is investigating how the most common genetic cause of #MND #FTD, called C9orf72, leads to the disease. 🧬 Using these findings, she is also looking at ways to correct the damage. Read more in our latest blog ⬇️ mndresearch.blog/2024/08/08/…
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Mandy Spencer and @nickjamescole kicked off #MNDEnCouRageUK by highlighting the importance of training the next generation of #MND #ALS researchers. One of these researchers could be the key to finding effective treatments or even a cure!
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“It’s easy to go and sit in the lab, and get good at science, but unless you can communicate that science there’s no point having done it.” #MNDEnCouRageUK aims to give #MND #ALS early career researchers the skills to communicate their research to the people it matters most – people affected by the disease. Read more: mndresearch.blog/2024/07/18/…
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“I’m trying to develop early-stage diagnostic tests so that we can regain 𝐩𝐫𝐞𝐜𝐢𝐨𝐮𝐬 𝐭𝐢𝐦𝐞 we are losing in the diagnostic process.” @beccysaleeb is one of more than 250 @mndassoc supported researchers. Read about her #MND #ALS research ⬇️ mndassociation.org/research/…
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#ResearcherSpotlight💡 In #MND, a gene called TBK1 becomes overactive in cells which help keep motor neurons healthy, known as microglia. Dr Gerbino is investigating whether reducing the activity of TBK1 could slow disease progression. Learn more ⬇ mndassociation.org/research/…
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In the last 10 years @mndassoc research portfolio has almost trebled to over £21 million. Thanks to your generous support we are funding more motor neurone disease #MND #ALS research than ever before. 🧡💙 Read about the innovative research we fund: mndassociation.org/research/…
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𝐎𝐯𝐞𝐫 𝟐𝟓𝟎 researchers are involved in @mndassoc research grants. 🔬 @RoisinTCDNeuro is investigating new ways to predict symptoms and help provide people with #MND #ALS more information on diagnosis. Listen to Roisin below to find out more about her research ⬇️
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What do roads, movies, maps and cake have in common❓ They were all used by our amazing early career researchers to help explain complex #MND #ALS research! 🔬 Well done to all our speakers who gave amazing talks! 🎉 #MNDEnCouRageUK
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𝐋𝐚𝐭𝐞𝐬𝐭 𝐍𝐞𝐰𝐬 @mndassoc funded researchers at @aberdeenuni have identified a new target for #MND #ALS therapies which, in the future, could lead to effective treatments for MND. They found that drugs which help Vitamin A to work in the body might help to protect neurons from damage. Read more: mndassociation.org/research/…
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Providing support for #MND carers is vital. @MND_peerSupport are testing a new online peer-to-peer support programme. They are looking for current caregivers and people who have experience caring for someone with MND to test the programme. More info ⬇ mndassociation.org/research/…
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Finding new treatments for #MND #ALS cannot be achieved in isolation. @mndassoc are proud to work alongside other partners to continue to strengthen and transform the world leading research carried out in the UK. 🤝 Read about our partnerships here: mndassociation.org/research/…
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Communication is key. 🔑 It is so important for #MND #ALS researchers to be able to talk about their research with the community. This research could impact their lives. At #MNDEnCouRageUK today, delegates heard all about how to give engaging talks from @SimonHallNews.
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We are proud to support @mndsmart - the first UK wide platform clinical trial for #MND #ALS. Find out more about MND SMART and other research projects we are funding to push forward the fight against MND here ⬇️ mndassociation.org/research/…
We have now randomised over 850 participants across all 4 UK nations. Sincere thanks to every person with MND who has contributed, their families, local research delivery teams, funders, & collaborators @EuansCentre @MNDScotland @MNDoddie5 @ADFoundationUK @MRCCTU @UKDRI
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What is a biomarker❓ A biomarker is a unique signal of #MND #ALS within the body. They can help improve diagnosis and to see if a drug is working. Hear more from @mndassoc funded researcher @DrEleniChristof who is hunting for biomarkers 🔎⬇️ mndresearch.blog/2024/08/29/…
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"By investing in these talented individuals, we are investing in a cure for MND – one of the people in the room could go on to find the key we all desperately want." We were blown away by the passion and dedication of the #MND #ALS community who attended #MNDEnCouRageUK last week. Read more about the event below ⬇️
Last week, early career researchers took to the stage at @mndresearch's MND EnCouRage UK 2024! Read the full story to learn how these young scientists are shaping the future of MND research and driving us closer to a cure below 👇
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Over 6,000 people have been recruited onto the MND Register, which aims to: 📍 Pinpoint how many people have #MND #ALS in England, Wales and Northern Ireland 🔬 Be a hub for research studies 🧑‍⚕️ Improve care planning Learn about the research we fund ⬇️ mndassociation.org/research/…
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What is translational research? 🔬 It bridges the gap between lab-based research and clinical trials to bring new potential treatments to people with #MND #ALS. You can read about the innovative translational research @mndassoc funds in our new report⬇️ mndassociation.org/research/…
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Today we are in Newcastle catching up with some of our amazing @mndassoc funded #MND #ALS researchers. Their research includes 🧪 new methods to improve diagnosis 🔬 understanding the impact of TDP-43, which is faulty in 97% of MND cases 💉 developing a potential treatment
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.@EXPERTS_ALS aims to rapidly screen potential new drugs using a marker of nerve damage. Neurofilament levels can indicate how much damage is happening to motor neurons and give us an indication is a treatment should be prioritised for further testing. 🧪 Find out more ⬇️
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Do you want to know more about #MND #ALS research but not sure where to begin? 🤔 We are taking it back to basics in our blog series to help everyone in the MND community more easily understand the latest research. 🔬 Check out our blog series ⬇️ mndassoc.org/back-to-basics
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“My work is driven by a great degree of hope and passion, and it was excellent to share this with those affected by MND.” Our #MNDEnCouRageUK event brings together the whole #MND #ALS research community. Read about Abby’s experience: mndresearch.blog/2024/09/12/…
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The world of clinical trials can be a daunting place. Here is an ongoing thread of some of the key terms and abbreviations to help de-mystify clinical trials 🧵⬇️ #ClinicalTrials101
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📣 Introducing our new #MND #ALS blog series! 📣 We’re taking it back to basics to break down the complexities of MND research to help the community follow the latest research more easily. Start exploring MND research 🔬 ⬇️ mndassoc.org/back-to-basics
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At #MNDEnCouRageUK today we heard exciting research from some of the brightest #MND #ALS early career researchers. Every day, all around the world, researchers are working hard in the fight against MND. 🌍 Stay up to date with the latest news here ⬇️ mndassociation.org/research/…
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The @UKMNDRI aims to coordinate #MND #ALS research in the UK and accelerate the search for effective treatments. 🔬 Bringing together the whole MND community, all with the same goal, is key to ending MND. The Institute features in our new report ⬇️ mndassociation.org/research/…
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#ResearcherSpotlight 💡 Our brain needs lots of energy to communicate with the body. 🧠 Dr Kiterie Faller is investigating whether brain cells get enough energy in #MND #ALS. Researchers could then look for ways to combat lack of energy. More: mndassociation.org/research/…
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Supporting psychological wellbeing is critical for people with #MND #ALS. Psychological support has been shown to make a real difference. A project supported by @mndassoc aims to develop guidelines on how to better deliver psychological support. More: mndresearch.blog/2024/07/25/…
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Here come the lightning talks! ⚡️ Each early career researcher has just 3 minutes to present their #MND #ALS research. We can’t wait to hear about the exciting research happening all over the UK! 🔬 #MNDEnCouRageUK
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#ResearcherSpotlight 💡 In motor neurone disease (#MND #ALS) an important transport system in the motor neurones doesn’t work as well as it should. @AndrewTosolini is investigating why this happens and if it can be corrected. 🔬 Read more: mndassociation.org/research/…
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Motor neurones send messages to muscles to tell them to move. 📨 In motor neurone disease (#MND #ALS) the neurones become damaged and die, stopping messages from reaching muscles. Find out what happens to neurones in MND⬇️ mndresearch.blog/2024/08/14/…
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Why become a Symposium Communications Ambassador? Hear why @drbenpchall became an Ambassador last year, and why you should apply ⬇️ More info: symposium.mndassociation.org… #alsmndsymp #MND #ALS #sciencecommunication #researchskills
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Are you an early career #MND #ALS researcher? Attending #alsmndsymp? Want to develop your science communication skills? Apply to be a Symposium Communications Ambassador and help us share the latest research from the largest conference dedicated to ALS/MND! More info: symposium.mndassociation.org…
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Absolutely thrilled to have Simon at #MNDEnCouRageUK. He gave an amazing workshop on how to communicate effectively and we can’t wait to see the presentations from early career researchers tomorrow! Thank you so much for spending your time with us. 💙🧡
The best work is when you really feel you’re making a difference. So as someone who, like far too many… Has lost family to the horrors of motor neurone disease. I could not be more proud to spend my week… Teaching @mndassoc scientists how to communicate their critical work.
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“While we work hard for a cure, it is essential we support those living with MND now” - @profcjmcdemott A new psychological therapy, called Acceptance and Commitment Therapy has been found to improve quality of life for people with #MND #ALS. Read more: mndresearch.blog/2024/07/25/…
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Prof Martin Turner also discussed his thoughts on how we can start to potentially move towards prevention of #MND #ALS for those who are at genetic risk of the disease. He highlighted the importance of working alongside people with an increased risk. #MNDEnCouRageUK
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#ResearcherSpotlight 💡 Genetic testing can help see if a person has a gene change associated with #MND. 🧬 Dr Alisdair McNeil (@am_sheffgenet) is developing a new decision aid which aims to help people make decisions around genetic testing. Read more: mndassociation.org/research/…
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The world of #clinicaltrials can be a daunting place. To help de-mystify clinical trials we will be breaking down some of the key terms and abbreviations in our #ClinicalTrials101 series. Make sure you follow the # to stay up to date!
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We're thrilled to support @jbneuro and Dr Ivo Lieveram in a new project alongside @The_MRC. The team are investigating what happens in the early stages of #MND #ALS. Specifically looking at the axons, which play a critical role in carrying electrical signals through the neurone. ⚡
📣 Congratulations to Prof Juan Burrone @jbneuro and Dr Ivo Lieberam! 👏 Their research into axonal dysfunction in ALS/FTD was awarded £3.9 million by the Medical Research Council and the MND Association. Read the story ⬇️ buff.ly/4bZwiDi #ALS #MND #FTD
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We are funding more research into motor neurone disease than ever before. 🔬 This is only possible thanks to every single person who supports us and raises awareness. Thank you, together we can beat MND. 💙🧡 #MND #ALS #research
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We kicked off day 2 of #MNDEnCouRageUK with media workshops! 📹 practising sharing their research through video interviews 📱coming up with engaging social media posts to share complex research Thanks for all the early career researchers for embracing it and getting involved! #MND #ALS #mediatraining
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𝙇𝙖𝙩𝙚𝙨𝙩 𝙣𝙚𝙬𝙨 Researchers have identified markers of #MND #ALS within the blood which, in the future, could have the potential to help diagnose MND. 🧪 More research is now needed to further develop this into a test which could be used at the start of the diagnostic process. Read more: mndassociation.org/research/…
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Programme now online! 🌐 Still not sure about attending the 35th International Symposium on #ALS/#MND? Check out our lineup of amazing speakers and find out what will be discussed in Montreal ⬇️ symposium.mndassociation.org… #alsmndsymp
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What is translational research? 🔬 It bridges the gap between lab-based research and clinical trials, to bring new potential treatments to people with #MND #ALS. Discover the innovative translational research @mndassoc are funding in our new document ⬇️ mndassociation.org/research/…
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Fantastic to see this £2million investment to help accelerate #MND #ALS research using large-scale data approaches. The initiative, launched by @HDR_UK and @DementiasUK, and supported by @UKDRI, is part of the £50 million pledged by the government after the #United2EndMND campaign.
We've launched MND Research Data Catalyst jointly with @HDR_UK. Accelerating discoveries in diagnostics & treatments for MND patients by harnessing large-scale health data infrastructure. zurl.co/RKfR #MND #research #data
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#MND #ALS clinical trial results can sometimes lead to sensational headlines 📰 On our blog we discuss a statistic often used to report on the outcome of #clinicaltrials and why it’s important to delve a little deeper. Read more: mndresearch.blog/2024/03/06/… #Statistics
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The 2nd UK PLS Day brings together people with Primary Lateral Sclerosis, a type of #MND. 🗣 Research and care updates from experts 📆 25 September, @NDCNOxford @mndoxford 🌐 Online viewing available: us06web.zoom.us/j/8505432419… Find out more ⬇️ ndcn.ox.ac.uk/research/oxfor…
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Looking to connect with #ALS #MND researchers, health and social care professionals, charities, people affected by the disease and more? Join us at the International Symposium on ALS/MND in Montreal, Canada in December. 🇨🇦 Register today: symposium.mndassociation.org… #alsmndsymp
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▪️Should placebos be included in a #clinicaltrial? ▪️should we carry out trials for drugs with a small effect or concentrate on finding a cure? These were just some of the questions @AmmarAlChalabi asked to all our delegates. Some fascinating conversations and perspectives from early career researchers and people affected by #MND #ALS. #MNDEnCouRageUK
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📢 Participants needed! 📢 Understanding what goes wrong in #MND is key to finding effective treatments. @PolitisNIG are using brain imaging to identify and track potential mechanisms of MND. 🧠 Contact @DeNataleER or more info ⬇️ mndassociation.org/research/…
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#ScienceCommunication can help you see the impact of your research. 🔬 Join us as a Symposium Communications Ambassador and hone your skills in communicating complex research through: 📱Social media ⌨️ Blogs 📹 Interviews Apply: symposium.mndassociation.org… #alsmndsymp #ecrchat
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It’s #ResearchAppreciationDay! 🔬 Research is key to finding effective treatments of #MND #ALS and achieving our vision of a world free of MND. Follow us to hear the latest updates and find out about the research @mndassoc fund!
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A massive thank you to @lifearc1 for their support at #MNDEnCouRageUK! 👏
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.@KristianaSalmon gave us a whistle stop tour of her career so far, including all of the twists, turns and pivots at #MNDEnCouRageUK. She also gave some good advice: “Your career doesn’t always go the way you think, timing isn’t always perfect and you have to make the choices that are right for you.” #MND #ALS #CareerDevelopment #CareerOpportunities
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Are you living with SOD1 #MND #ALS in the UK? Join us in calling on NICE to make tofersen available on the NHS. ✍️ Sign our open letter 📧 Email kielan.arblaster@mndassociation.org
We are seeking people living with SOD1 MND in the UK 📢 Clinical trial results for Tofersen show great promise. People have reported slower deterioration of their condition and, in some instances, their progression stopping altogether.
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What do golden retrievers have to do with #MND #ALS? 🐶 The early career researchers used all kinds of analogies today to help explain their research at #MNDEnCouRageUK today. From methods to help predict disease progression, to improving quality of life to finding effective treatments, we heard it all! 🔬
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Got a question about #MND #ALS research? Don’t quite understand a specific topic? 🔬🧪 Let us know and we’ll look at including it in our new Back to Basics blog series. Check out the series so far here ⬇️ mndassoc.org/back-to-basics
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Presenting at conferences is a great way to develop new connections 💡 Why not present your research at the largest conference dedicated to #ALS/#MND research. 📆 Deadline: 11 July (23:59 BST) Submit today ⬇️ symposium.mndassociation.org… #alsmndsymp #ResearchAppreciationDay
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#ResearcherSpotlight 💡 MND can affect each individual differently. Dr David Lester is looking for clues to explain these differences, identify patterns and potentially subgroups. 🔎 This could lead to personalised treatments for #MND #ALS. More: mndassociation.org/research/…
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💥 Applications for @mndassoc biomedical research grants are now open! 💥 Do you have an idea which could increase our understanding of #MND #ALS or potentially be a treatment? 🔬 🗓 Apply before 1 November Learn more ⬇ mndassociation.org/research/…
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Fantastic to see international researchers working together in the fight against #MND #ALS, including some researchers who have been supported by @mndassoc. Collaboration is so vital in research!
Very excited to receive funding from @TargetALS_fdn for our international consortia between @SinaiBrain , @UCLIoN and @UKDRI at Edinburgh. @RickiePatani, @HaselPhilip , Andrea Malaspina, really looking forward to working with you all!
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Looking to keep up to date with the latest #MND #ALS research? Hear results from clinical trials, updates from labs all over the world and more. 🔬 Sign up to our Research Monthly newsletter to get the latest research straight to your email! 📩 ⬇ mndassociation.org/research/…
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📢 Participants needed! 📢 @Opti_cals is a clinical trial investigating whether a tailored, high-energy diet alongside a tool to support nutrition could slow down #MND #ALS disease progression. Learn more about how to take part ⬇️ mndassociation.org/research/…
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#ResearcherSpotlight 💡 @GHautbergue is developing a potential gene therapy for the most common genetic form of #MND #ALS. Learn more and how we work in partnership with others like @lifearc1 to fund the most promising research in our new report 👇 mndassociation.org/research/…
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.@MarieCurieEOLC are looking to hear from people affected by #MND #ALS to help shape future research into palliative and end of life care. Have your say by taking part in their survey 💬 ⬇️ bit.ly/3Ln1XUA #PeolcPSP
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“I have always had a keen curiosity for all things science. When my mum was diagnosed with ALS in 2007, this only added fuel to the fire.” Abby O’Sullivan is trying to identify new combinations of drug treatments for #MND #ALS. Read more: mndresearch.blog/2024/09/12/…
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We're thrilled to see research we helped kickstart being taken to the next stage and investigated further! 🔬 Congratulations @AlfredoIacoange!
Huge thanks to @MNDScotland & @mndassoc for supporting the preliminary work that led to this award.I cannot wait to start working on this with @psychgenomics @AmmarAlChalabi @AhmadAlKhleifat @tammarynlashley @richdobson @NoncodingDNA @SulevKoks @KCLBHI @NIHRMaudsleyBRC @kingsmnd
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Today is #WorldBrainDay! 🧠 Researchers are developing new ways to study the brain in the lab, by growing brain cells in a dish. These models will more closely mimic the cells in the body and help us learn more about what goes wrong in #MND #ALS. More: mndresearch.blog/2024/03/14/…
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How do we know if a #clinicaltrial has been successful? Researchers decide what the aim of the trial is, such as slowing disease progression. A measurement or primary endpoint is used at the end of the trial to see if the treatment hit this aim. #ClinicalTrials101 #MND #ALS
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We want to keep early career researchers in #MND #ALS research. The final session of day 1 of #MNDEnCouRageUK focuses on navigating careers. Kicking us off is James Connell from @lifearc1 discussing alternative career paths. Thanks to @lifearc1 for their support of MND EnCouRage.
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What is a placebo? 💊 A placebo is a ‘dummy drug’ which looks and tastes the same as the treatment being tested. Placebo groups are used in clinical trials to ensure any beneficial effects observed are entirely down to the treatment. #ClinicalTrials101
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Clinical trials are time-consuming and expensive but vital in the hunt for #MND #ALS treatments. Innovative trial designs can: 💊 test multiple drugs at the same time ↗️ help prioritise which drugs to test further Learn how we support new approaches: mndassociation.org/research/…
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Find the clinical trial process confusing? 😕 Not sure what all the different terms and abbreviations mean? Not sure where to start to find information? Check out our #ClinicalTrials101 thread! We add to it every week. #MND #ALS
The world of clinical trials can be a daunting place. Here is an ongoing thread of some of the key terms and abbreviations to help de-mystify clinical trials 🧵⬇️ #ClinicalTrials101
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Presenting your research isn't just about the content, its also about your presence! At #MNDEnCouRage Rebecca Saleeb took the opportunity to get some advice from @SimonHallNews. Read more below ⬇️
A trick of IT can transform your presentations. I saw it in full and glorious action when teaching at the Motor Neurone Disease Association researchers’ conference. To reveal the insight… And enjoy its impressive effect… See this lovely guest blog: thetvdetective.com/blog/brea…
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The team is working hard behind the scenes in preparation for #MNDEnCouRageUK tomorrow! The event aims to encourage early career researchers to stay in #MND research and connect them with people living and affected by MND. Stay tuned for updates from the next 2 days! 👀
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All around the world researchers are working hard to find effective treatments for #MND #ALS and improve the quality of life for people living with MND and their families. 🌍 Stay up to date with the #LatestNews over on our website ⬇️ mndassociation.org/research/…
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