Looking for a last minute Xmas 🎁? How about my book, The Explorer and the Journalist? It’s the story of the explorer lauded as a hero for becoming the first person to reach the North Pole, and the journalist who risked his career to prove he was lying… amazon.co.uk/Explorer-Journ…

There are lots of #2024Predictions on here today, and so I thought it would be interesting to go back to the start of 1939, a year that brought global calamity, and see what newspapers were saying at the start of it... 1/8

'It's incredibly fitting that Kevin and the team are setting off from our office' Richard Evans from the MND Association spoke to #BBCBreakfast as rugby league legend Kevin Sinfield began day 6 of his week long ultra marathon challenge from their HQ in Northampton, heading to

Kevin, what you are doing is inspirational. As you embark on the final leg of your challenge today, I send a massive thank you, for your dedication and commitment to such an important cause.

✅ 7 ultra marathons ✅ 7 days ✅ 7 UK regions No matter the weather, no matter their injuries - always running for the #MND community, raising £1 million. A remarkable seven days #RunningHomeForChristmas. Thank you Kev, Chris and Dave on behalf of the #MND community!

May you all enjoy #NewYear2025 as much as people at Royal Albert Hall looked like they were enjoying the start of 1935

H G Wells: “[There was no] perceptible limit to the amount of misdirection and social disorganisation that could be achieved by sustained lying.”

🚨Delighted to share that my new book, Interviewing Hitler, will be published in August. It’s the story of how George Ward Price became the world’s leading journalist in the 1930s through a series of interviews with Hitler. Available for pre-order now 👇 amazon.co.uk/Interviewing-H…

Our Director of Engagement, Richard Evans, spoke with Sky News earlier about access to tofersen for those with the SOD1 variant of MND. He was joined by Seckin, who has #MND and has been told she can’t have tofersen due to NHS resource constraints. This is simply unacceptable.

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

The MND Association is proud to be a principal funder of the Longitude Prize on ALS, delivered and designed by Challenge Works and supported by Nesta 🔬 You can find out more about the prize, and what it aims to do, here 👇🏼 bbc.co.uk/iplayer/episod…

Heard that my new book, Interviewing Hitler, has been sent to the printers today! Exciting milestone, ahead of publication at the end of August!

In this article shared with the Times, Geoff Burrow, Rob Burrow’s father, shares his frustration at the lack of access to tofersen for those living with SOD1 MND. Read more ➡️ thetimes.com/comment/column…

If you have not signed already, then PLEASE sign now 🙏 You might, literally, be a Life Saver 👍

In this episode of MND Matters, our Chief Executive Tanya Curry and Director of Engagement, Richard Evans, reflect on a transformative year for the MND Association. From expanded grants, the launch of our Research Nurse Network and more. Hear the latest below. 🎧 #MNDMatters

We at MND Association have brought an ice sculpture of Seckin, one of the patients unfairly being denied the lifesaving drug tofersen, to Westminster. We’re urging the Govt to insist the postcode lottery ends. R/T if you agree!

People with SOD1 MND don’t have time to wait. #PrescribeLife 📍Parliament Square Gardens, Westminster

Review of my new book in the Guardian 👇

Dear Wes Streeting, Tofersen is life-saving, and free, yet around 20 people with SOD1 MND are being denied access to it. They do not have time to wait. You’ve got the power. Please use it. #PrescribeLife