“Sometimes”, Ed? Rest isn’t an occasional luxury. It’s a basic human need.
Unpaid carers can provide 100+ hours of care a week, yet must undergo assessments to establish their need for support, including respite.
What paid employee has to prove they need a break?
Rae :-) retweeted
Require venues to accept government evidence of disability or caring needs petition.parliament.uk/petit…
Rae :-) retweeted
We shouldn’t need to petition parliament. Where is the @EHRC on the subject of many venues demanding we buy a £15 access card in order to get reasonable adjustment under the Equality Act?
Require venues to accept government evidence of disability or caring needs petition.parliament.uk/petit…
“MUST have registered for a Nimbus Disability Access Card.”
Why, @YorkBarbican?
Disabled people have rights under the Equality Act 2010. Accessibility is a legal duty, not a membership scheme.
Rae :-) retweeted
A reminder to @Helen_Whately and other politicians hell bent on cutting critical services and support, that treating welfare reform as nothing more than a cost-saving exercise has very real human consequences.
In 2010, Scottish poet Paul Reekie took his own life, aged 48.
He left no suicide note.
Instead, on his desk were two letters. One informing him that his incapacity benefit had been stopped. The other informing him that his housing benefit had been stopped.
His GP subsequently raised his death as a warning about the consequences of welfare reforms.
This is what gets lost when politicians reduce disability, illness and poverty to numbers on a spreadsheet.
We're talking about people who depend on this support to survive. People already facing enormous challenges, who are then pushed further into poverty, insecurity and desperation by decisions made in Westminster.
Of course we should all want a welfare system that works better. But reform should be about improving people's lives, providing meaningful support and addressing the reasons people need help in the first place.
That means creating genuine opportunities for those who can work, removing the barriers that prevent them from doing so, and ensuring that those who can't work have the security, dignity and support they need to live fulfilling lives.
The measure of success can't simply be how much money the Treasury saves. It must be how many lives we improve, how many opportunities we create, and what happens to the people whose support is taken away.
The human cost of getting that wrong is irreversible.
Rae :-) retweeted
Replying to @Helen_Whately
Oh my goodness! There was I thinking at 16 she would magically be able to walk and talk. Given it’s only 2 weeks away it’s maybe not quite realistic though.
Suggestion, @Helen_Whately. Rather than focusing on the cost of disabled people, why not focus on the systems failing them?
NHS clinical negligence payments rose from £863m in 2010/11 to over £3bn in 2024/25, - 14 yrs of Conservative government
Where was the accountability?🪡
How much lifelong disability, social care & welfare spending could be prevented by tackling medical negligence?
@Helen_Whately, rather than questioning support costs, what reforms would prevent harm?
Fix the failures. Don’t blame those living with the consequences.
Hey @CostaCoffee, why advertise your St James’s Hospital, Leeds (Bexley Wing) café as open until 6pm on Sundays when it regularly closes earlier (hour + earlier today)?
Patients & visitors make the effort to walk down, often from wards some distance away, only to find it shut.
Shameful framing from @SkyNews.
Why compare 180,000 armed forces personnel with 430,000 young people claiming PIP?
PIP isn’t unemployment benefit. Disability isn’t a choice.
Disabled young people aren’t responsible for Britain’s defence budget. Stop portraying them as a burden
Rae :-) retweeted
Disgusting gutter journalism on Sky this morning. Comparing the size of the army to the small amount of young people (less than 6%) on pip with the implication Disabled people are holding back defence spending. I hope what they pay is worth it @ayeshahazarika. @InclusionLondon
Good morning, @Helen_Whately.
A little Sunday morning question for you.
Do you realise how hurtful your comments about disabled children continuing to receive benefits as adults are to families?
What exactly do you imagine happens to their lifelong disabilities at 18?🪡
If courts can calculate the enormous lifelong cost of profound disability, why aren’t those judgments informing government policy?
They show exactly what care, equipment and therapies cost, and what families face trying to secure them.
Why aren’t we learning from that?🪡
Tackle NHS negligence & social care failings @Helen_Whately
ALL families deserve proper support, without begging charities or fundraising for essentials
Disabled children become disabled adults, often with greater needs when the right support wasn’t provided early on.











