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It was a pleasure to welcome Liz Twist MP to our Parliamentary drop-in today to meet some of our team and hear about the Association's campaigning priorities. We look forward to working together in the future to make change for the MND community. #GlobalMNDAwarenessDay

We would like to say a massive thank you to all the MPs and representatives from the MND community who attended our #GlobalMNDAwarenessDay Parliamentary drop-in event today. 🧡 The event gave MPs a chance to hear about the lived experiences of those with MND, and find out what

We're very grateful to the Minister of State for Social Security and Disability Sir Sir Stephen Timms for taking the time to talk to Seckin about her journey with SOD1 MND and her fight to access tofersen. We look forward to working with Minister to ensure everyone living with MND

We’ve submitted our response to the London Plan consultation. We’re calling for the Mayor to deliver on the 10% M4(3) wheelchair accessible homes pledge and extend these standards across all housing tenures — not just affordable housing. London must build homes that truly meet

This week our Chair lan Byrne MP & Vice Chair Aphra Brandreth attended the MND Association's parliamentary event to mark #GlobalMNDAwarenessDay. The APPG is committed to continue shining a light on the hidden realities of #MND in parliament and beyond. #MNDHiddenRealities

As a person living with #mnd #als - this choice means so much to me. Now, come the time that life becomes intolerable, I won’t have to consider travelling to end my life with dignity. Infact I may never have to now. Now, there is no stopping dignity. Historic humane vote.

Tacrolimus added as the fourth investigational arm in MND-SMART. MND-SMART uses an innovative #MAMS design to evaluate several potential treatments simultaneously, speeding up the time to identify effective therapies. Read more 👉 edin.ac/4jWf0uM #GlobalMNDAwarenessDay

As we approach #globalmndawarenessday tomorrow, I just wanted to share a few thoughts True Anna style, I tried to record myself but as MND takes over I didn’t think involuntary smiling and laughing was appropriate Please take some time tomorrow to think of the #mndcommunity

Please "Prescribe Life" for Seckin & other @MNDpatients with SOD1 gene mutation on #MNDglobalawarenessday by signing this petition act.mndassociation.org/2025-prescribe… Darby Rimmer MND Foundation Ed Slater Geoff Burrow Charlotte Hawkins Mike Wilson* Lynn Pritchatt Cris Hoskin Eleanor Dalley

Today is #GlobalMNDAwarenessDay - a day to honour everyone affected by motor neurone disease. This APPG is committed to raising awareness of the challenges the #MND community face in parliament and beyond. Find information and support via the MND Association & MND Scotland websites.

FOR ME, every day is #MND Awareness Day. BUT, TODAY is the official one. NO WORDS can adequately describe the true horror of this callous killer without a cure! FLY FREE, Dad, destroyed by #MND almost twenty years ago.... 😢 #MND #MoreNeedsDoing! #GlobalMNDAwarenessDay

Delighted to see this investment in MND Research by Darby Rimmer MND Foundation. Huge thanks to all participants in various mega-treks. This helps accelerate progress towards meaningful treatments & is a great boost to the efforts of UK MND Research Institute Kevin Darby Mike Wilson* Oliver Kay Chris Kirkland

Emma_MacLennan MND Association Darby Rimmer MND Foundation MND Scotland My Name'5 Doddie Foundation Challenging MND FightMND Neale Daniher Sam Burgess Sir Bill Beaumont MND Research Australia Thank you, Emma and David. Love to you both too. And remembering Alex, your beautiful boy. 💔🫶 #GlobalMNDAwarenessDay

My silence isn’t a choice. If you had 21 seconds left to speak what would you say? 😶 Take 21 seconds of silence. 📱 Text '21SECONDSFORMND' to 70560 to donate & help 🫂 Nominate 3 friends to do their 21 second silence #GlobalMNDAwarenessDay

🏉 JOOST VAN DER WESTHUIZEN'S tweet on #GlobalMNDAwarenessDay eleven years ago today. Joost lost his life to merciless #MND in February 2017.... 😢 #MND #MoreNeedsDoing!

Today is #GlobalMNDAwarenessDay. MND isn’t incurable, it’s just underfunded. Research gives hope. Funding makes it possible. #ALS #MND

Tonight, Roath Park Lighthouse will be illuminated in vibrant shades of blue and orange to mark #GlobalMNDAwarenessDay and to raise awareness for motor neurone disease. 💙 🧡 For more info, visit: orlo.uk/Z18Gq #MND MND Association | Cymru Wales MND Association

We asked the MND community what they wish people knew about #MND. What’s one thing you wish everyone knew about motor neurone disease? #HiddenRealities #GlobalMNDAwarenessDay

We are saddened to hear the news that former cricketer David ‘Syd’ Lawrence MBE has died, one year after being diagnosed with motor neurone disease (MND). Our thoughts are with David’s family and friends at this difficult time.

🏏 Shocked and saddened to hear that former @EnglandCricket paceman DAVID 'SYD' LAWRENCE has succumbed to #MND, aged 61. Although inevitable, I always want to believe our incredible #MND Warriors are immortal. Fly free, David... 😢 #MND #MoreNeedsDoing! bbc.co.uk/sport/cricket/…