Doddie worked tirelessly to raise awareness of #MND. His fundraising and campaigning will help move MND research forward. Our thoughts are with his family and friends.
@AXS_UK Terrible customer service. Been trying for months to access my sold ticket funds (£300). Not able to talk to anyone and live chat is hopeless. Don’t use this company.
@axs@axsuk Terrible customer service. Been trying for months to access my sold ticket funds (£300). Not able to talk to anyone and live chat is hopeless. Don’t use this company.
@axs - Terrible Customer service. Been trying for months to access my sold ticket funds (£300). Not able to talk to anyone and live chat is hopeless. Don’t use this company.
It's 19 months since the Govt promised to review benefits for terminally ill people.
Since then, as many as 5,000 people may have died waiting for benefits. @SteveBarclay, please will you urgently approve @DWP's proposed changes? #Scrap6Months#MND https://t.co/nDJddFw9Mu
URGENT: Thanks to our #Scrap6Months campaign,@DWP review into benefits system for terminally ill people is complete, but awaiting @hmtreasury approval.
❗️We only have 2 weeks to get MPs to write to the Treasury asking for urgent approval. Email yours👇🏼 https://t.co/M1sVl6fgar
@SportsDirect_CS Really appalled by the customer service at sports direct. Waiting for months for a resolution with a faulty product. CAS -5212397-Z1V9C0
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. https://t.co/oMDYuFMWWO
At the moment in the UK, people with #ALS#MND have to prove "a reasonable expectation of death within 6 months" to be eligible for financial support from @DWP. This is inhumane for someone already dealing with a devastating diagnosis. #Scrap6Months@theresecoffey@mndcampaigns
The raw power of Rosie Duffield's speech in the domestic abuse debate. 💪🏻😢💕
This is a must-watch. Absolutely riveting, it opens a window into the experience of far far too many people, mostly women. Thank you @RosieDuffield1 for sharing this.
It is inhumane that someone with a life limiting illness has to wait to have home adaptations that will enable them to live with dignity and independence. Well done to @NeuroAlliance member @mndcampaigns for highlighting such an important issue.
The Prime Minister must resign to make way for an emergency Government that can stop a No Deal Brexit. The @LibDems will keep fighting for People’s Vote and to stop Brexit altogether.
Did you know that motor neurone disease is categorised as a rare disease?
A person's lifetime risk of #MND is around 1 in 300. Not enough people are aware. This #RareDiseaseDay let's change that!
Retweet our info-graphic explaining some of the key facts! #RareDiseaseDay2019
Let's start 2019, our 40th year, how we mean to go on... 📣
Help us raise awareness of motor neurone disease. Please retweet our graphic which highlights all the key facts about #MND that people may not know.
Our vision is a 🌎 free from MND!