The Neurological Alliance

📨Thank you. Over 3,000 people signed our open letter to the Secretary of State for Health and Social Care. Together, we've made a powerful statement. Read the letter here: bit.ly/4o1KXVC Watch this space for further updates.

To mark World Brain Day 2025, we're delighted to share Brain Health Matters podcast – 'Invisible Battles: The Unseen Realities of Neurological Conditions'. bit.ly/40rRu1V #WorldBrainDay #WorldBrainDay2025 #MyalgicEncephalomyelitis #MultipleSclerosis

CLOSES MIDNIGHT TONIGHT: Sign our open letter and tell the government to act now to improve workforce and services for the 1 in 6 people living with a neurological condition and their loved ones. Follow this link to sign now: bit.ly/ActForThe1in6 Thank you!

Last chance to sign! Add your signature to our open letter to Wes Streeting and tell him: to improve healthcare for people affected by neurological conditions we need action from government now, not just words: ✒️ bit.ly/ActForThe1in6

@NeuroAlliance: Tell the government to act now for the 1 in 6: sign our open letter Only 1 in 3 people with neurological conditions feel that their healthcare meets their needs, according to the My Neuro Survey 2024.  So the Neurological Alliance are asking for people to sign…

Follow this link to sign our open letter to the Secretary of State for Health and Social Care, Wes Streeting, now and tell him: Act now bit.ly/ActForThe1in6 Thank you

We need action from government, not just words. In My Neuro Survey, people most reported being unable to access specialist mental health support despite needing this. Sign our open letter to now. bit.ly/ActForThe1in6 Thank you.

We need action from govt, not words. Too many people affected by neurological conditions are still facing a reality where their needs are not met. Please sign our open letter to the Secretary of State for Health and Social Care and tell him: act now bit.ly/ActForThe1in6

We need action from government, not just words. In My Neuro Survey, people most reported being unable to access specialist mental health support despite needing this. Sign our open letter to now. bit.ly/ActForThe1in6 Thank you.

We need action from govt, not words. Too many people affected by neurological conditions are still facing a reality where their needs are not met. Please sign our open letter to the Secretary of State for Health and Social Care and tell him: act now bit.ly/ActForThe1in6

Sign our open letter here: bit.ly/ActForThe1in6 to the Secretary of State for Health and Social Care, Wes Streeting and tell him. Act now. In My Neuro Survey, people most reported being unable to access specialist mental health support despite needing this. Thank you

Our response to the NHS 10 Year Plan, published by @DHSCgovuk today. You can support our call by signing our open letter to Health and Social Care Secretary Wes Streeting today: bit.ly/ActForThe1in6

We need action from government, not just words. In My Neuro Survey, people most reported being unable to access specialist mental health support despite needing this. Sign our open letter to now. bit.ly/ActForThe1in6 Thank you.

The results are out: in our latest My Neuro Survey, just 1 in 3 people said the healthcare they receive meets their needs. There are opportunities to change this, but we need action, not words. Sign our open letter to government now here bit.ly/ActForThe1in6

The #WelfareReformBill was passed yesterday after the government agreed to halt any reform to personal independence payment (PIP) until after the Timms Review. This is powerful testament to what campaigning can do, but government concessions do not go far enough. STATEMENT👇

"My Neuro Survey exposes gaps in services" My Neuro Survey features in @ACNRjournal acnr.co.uk/my-neuro-surve… #ActNowForThe1in6

"By pushing the cuts onto future claimants, the government are betraying the next generation of disabled people. We urge MPs to use their power to stop this impending disaster." Read our response to the #WelfareReformBill ⬇️ @ParkinsonsUK #DisabilityBenefits

Charlotte and Katie told @BBCRadio4 about the devastating impact cutting disability benefits could have on people living with MS. “Disabled people pay on average an extra £1,000 a month just to get by.” 💳 Timestamp: 15.30s Tune in: mssoc.uk/45P0Msm (4/5) 🧵

The Government have showed us that they are starting to listen to disabled people. But the so called concessions they're offering are just not good enough. It's time to #StopTheCuts. ❌ Email your MP and help us protect disability benefits: mssoc.uk/46jRBQG (5/5)🧵

We need action from govt, not words. Too many people affected by neurological conditions are still facing a reality where their needs are not met. Please sign our open letter to the Secretary of State for Health and Social Care and tell him: act now bit.ly/ActForThe1in6