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So, who is going to employ all these disabled people the government wants to wean of welfare

1000 replies

Jimisnotmyname · 18/03/2025 16:14

Really wondering. Not saying it is necessarily a bad thing to encourage those who can work, to work but as a carer for 2 disabled family members, I am hugely struggling to find another job as nobody is willing to give me any flexibility (which I need as a carer) and there are always candidates who do not need the same accomodations I do. I would imagine that many of those currently not in work because of disability or a health condition, will often need a similar level of flexibility. I just wonder who on the the government think will offer jobs galore on these circumstances??

OP posts:
Thoughtsonstuff · 18/03/2025 22:15

EmeraldShamrock000 · 18/03/2025 22:10

There is no easy solution to the growing problem.
There is a huge increase in young people claiming anxiety related disability benefits that are keeping them restricted to a life of poverty, if the correct adjustments are made and anxiety diagnosis are dealt with early, many would have a better lifestyle than the circles of poverty, boredom, added depression.

CBT is being referred to in the news at the moment as something to try for those sorts of kids. It's not surprising after covid that young people are experiencing these sorts of things and I think the government need to make a real effort to support them better. Not making employing them harder by increasing Employers NI. It's massively in the country's long term interests that these kids get off benefits and have the incentives to work and gain experience.

MistressoftheDarkSide · 18/03/2025 22:16

In the run up to all this there were multiple threads about the proposed cuts, and on a couple I repeatedly asked the question where are all these super flexible and inclusive employers going to come from. Funnily enough despite repeatedly asking, people just kept being righteously ableist but couldn't actually answer the question.

It strikes me the question still isn't being actually answered. Lots of idealistic suggestions that overlook so many obvious pachyderms in the room.

The biggest one is that in the current economic climate, companies need to make maximum profit for minimum outlay, hence job cutting left, right and centre, plus the tinkering with NI and huge rates rises for business premises, not to mention the encroachment of automation and AI that is making certain industries virtually obsolete (no pun intended).

The employment market is changing at an exponential rate, and while it's laudable to think employers will want to embrace the disabled, the costs of reasonable adjustments will not be cost effective for many.

Someone else pointed out the disingenuous language this drive to "help" benefits claimants is being couched in. That it should be considered supportive and an extension of "therapy". Are employers really going to want to sink time and money into that at a time when their basic operating costs are being elevated?

Don't get me wrong, I'm all in favour of those who feel they can work being enabled to do so, and those who can't being supported to at least live like human beings, however, like everything else being proposed, there seems to be a populist wrecking ball being swung through the most vulnerable sections if society.

I also believe the pace and intensity and complexity of modern life, plus economic stress, is partly behind the apparently increasing numbers of the unwell and disabled. We have little idea of how our environment, with all the cumulative additives, chemicals, pollutants and toxins are truly affecting us, not to mention the potential legacy of over 3000 nuclear tests since 1945, above and below ground that could have impacted the earth and water.

The impact of technology from a neurological perspective is not yet fully understood, and while we are urged to limit screentime we are also hugely dependent on it for every aspect of modern life.

In terms of places of employment, my relatively affluent South coast university hometown has so many empty shops in the town centre, it's embarrassing. No department stores, even M&S have decamped to out of town retail parks and parking is a very expensive joke.

Call centre jobs are very hard to come by, and as others have mentioned, WFH is being phased out.

We're in a pretty pickle indeed, and I stand in solidarity with those on the lowest economic rung of the ladder, wondering where the hell the next rungs have gone.

The less money people have to spend, the more the economy will decline, and the more people will suffer.

JitterbugFairy · 18/03/2025 22:17

TheFairyCaravan · 18/03/2025 16:37

Care homes? I can’t walk unaided, in fact my elderly parents are more mobile than me, how would that work in a care home? I worked in education until I couldn’t drag myself in any longer. Not only that I’m not sure there’s many parents who’d be happy for their children to be looked after by someone who is on crutches and is likely to fall on their face at any time. I could take my wheelchair but most schools & nurseries aren’t accessible.

If that's the case,you wouldn't have your money stopped surely?

Juniegirl · 18/03/2025 22:20

Lourdes12 · 18/03/2025 22:05

I’m guessing she doesn’t have to deal with pain

Yes, my colleague takes various meds as she suffers nerve pain despite being paralysed. It’s not uncommon apparently.

She also always has sore, cracked hands, often burns herself on heaters or hot water bottles (she’s always freezing). These become infected occasionally.

Shes a trooper though.

Puyyt · 18/03/2025 22:20

JitterbugFairy · 18/03/2025 22:17

If that's the case,you wouldn't have your money stopped surely?

Her wheelchair is tied into motability, which isnt being affected

She could have lost her daily living points because of not getting 4 points in 1 descriptor, which is very common.

Most claims are made of of multiple low points rather than a few high ones.

I think thats exactly why the gov have implemented this. Its invalidates alot of claims

MrsPeregrine · 18/03/2025 22:21

Jimisnotmyname · 18/03/2025 16:14

Really wondering. Not saying it is necessarily a bad thing to encourage those who can work, to work but as a carer for 2 disabled family members, I am hugely struggling to find another job as nobody is willing to give me any flexibility (which I need as a carer) and there are always candidates who do not need the same accomodations I do. I would imagine that many of those currently not in work because of disability or a health condition, will often need a similar level of flexibility. I just wonder who on the the government think will offer jobs galore on these circumstances??

This isn’t a quick fix. No one is pretending it is. There are plenty of people on disability benefits who can’t work. But there are also plenty who can (with the right help and support framework in place).

Thoughtsonstuff · 18/03/2025 22:22

MistressoftheDarkSide · 18/03/2025 22:16

In the run up to all this there were multiple threads about the proposed cuts, and on a couple I repeatedly asked the question where are all these super flexible and inclusive employers going to come from. Funnily enough despite repeatedly asking, people just kept being righteously ableist but couldn't actually answer the question.

It strikes me the question still isn't being actually answered. Lots of idealistic suggestions that overlook so many obvious pachyderms in the room.

The biggest one is that in the current economic climate, companies need to make maximum profit for minimum outlay, hence job cutting left, right and centre, plus the tinkering with NI and huge rates rises for business premises, not to mention the encroachment of automation and AI that is making certain industries virtually obsolete (no pun intended).

The employment market is changing at an exponential rate, and while it's laudable to think employers will want to embrace the disabled, the costs of reasonable adjustments will not be cost effective for many.

Someone else pointed out the disingenuous language this drive to "help" benefits claimants is being couched in. That it should be considered supportive and an extension of "therapy". Are employers really going to want to sink time and money into that at a time when their basic operating costs are being elevated?

Don't get me wrong, I'm all in favour of those who feel they can work being enabled to do so, and those who can't being supported to at least live like human beings, however, like everything else being proposed, there seems to be a populist wrecking ball being swung through the most vulnerable sections if society.

I also believe the pace and intensity and complexity of modern life, plus economic stress, is partly behind the apparently increasing numbers of the unwell and disabled. We have little idea of how our environment, with all the cumulative additives, chemicals, pollutants and toxins are truly affecting us, not to mention the potential legacy of over 3000 nuclear tests since 1945, above and below ground that could have impacted the earth and water.

The impact of technology from a neurological perspective is not yet fully understood, and while we are urged to limit screentime we are also hugely dependent on it for every aspect of modern life.

In terms of places of employment, my relatively affluent South coast university hometown has so many empty shops in the town centre, it's embarrassing. No department stores, even M&S have decamped to out of town retail parks and parking is a very expensive joke.

Call centre jobs are very hard to come by, and as others have mentioned, WFH is being phased out.

We're in a pretty pickle indeed, and I stand in solidarity with those on the lowest economic rung of the ladder, wondering where the hell the next rungs have gone.

The less money people have to spend, the more the economy will decline, and the more people will suffer.

Agree. The government increase in Employers NI and immediate workers rights have stuffed the part time starter jobs that young people of any sort relied on, let alone those that are restricted by disabilities. There are too few jobs for too many people and that will get worse as low skilled immigration continues.

Interesting point re nuclear tests. I'd never clocked that. I think smartphones have fueled the increase in ADHD diagnoses in children. I'm an adult and I can't concentrate on a book any.more and I grew up without smartphones so goodness knows what the effect on children is.

Nadiaelgato · 18/03/2025 22:23

Thoughtsonstuff · 18/03/2025 22:09

I feel very sorry that you are in this situation. Clearly not everyone is genuine though.

The poor will just become poorer. There's an alternative option: tax the wealthy.

Thoughtsonstuff · 18/03/2025 22:27

Nadiaelgato · 18/03/2025 22:23

The poor will just become poorer. There's an alternative option: tax the wealthy.

It's self defeating unfortunately for all the reasons discussed relentlessly on these threads. The solution is an economy that generates more wealth. Unfortunately Labour haven't acheived that.as yet.

Kirbert2 · 18/03/2025 22:28

WinterBones · 18/03/2025 21:48

It isn't, not any more, research is moving along and new discoveries about it are being made, and have been made in the last year.

It's something that has very recently (literally last week) been floated by Pain Management clinic for me. Now i have a very real, identifiable chronic pain issue caused by degenerative disk disease and arthritis, i suffer with sciatica and have lost mobility in one of my hips. Alongside this i have a lot of as-yet unexplained joint pain, cramp, dysautonomia, migraines, paraesthesia in my hands/feet...etc

They know that Fibro is related to the brain, they know it's a dysfunction of the central nervous system, it becomes hyperactive and stops processing physical input correctly, and instead interprets it as pain. They know there are genetic factors for it.

My older brother has diagnosed ME/CFS that he developed post-viral (Guillain barre syndrome) and have directly told me that the fact he has that, genetically makes me more likely to have developed a similar CNS issue, especially with my already present neuropathy from my spine crumbling and my sensory processing issues from my Autism/ADHD.

My son has neuropathy too. He got it due to a side effect of been so unwell he was in intensive care for a number of weeks from complications caused by cancer.

Then once he was well enough, he started chemotherapy including one which is known to cause neuropathy so it saved his life but made his pain worse.

His left foot has improved but he still gets pain in his right foot and can't feel or move his toes at all.

cocoloco23 · 18/03/2025 22:29

Arcticrival · 18/03/2025 18:33

I don't think it's a bad thing. Of course there are many many genuine cases but there are also many many cases of people who have fudged the system as they get more money on disabled benefits thatn they would working.

Ime, some people will do anything they can to work and some people will do anything they can to not work.

Less than 4% of the benefits bills is awarded fraudulently. That’s the government’s own figures: https://www.gov.uk/government/statistics/fraud-and-error-in-the-benefit-system-financial-year-2023-to-2024-estimates/fraud-and-error-in-the-benefit-system-financial-year-ending-fye-2024

Fraud and error in the benefit system, Financial Year Ending (FYE) 2024

https://www.gov.uk/government/statistics/fraud-and-error-in-the-benefit-system-financial-year-2023-to-2024-estimates/fraud-and-error-in-the-benefit-system-financial-year-ending-fye-2024

WiddlinDiddlin · 18/03/2025 22:30

Ultimately theres two options.

1 - we accept that to avoid those truly in need of disability benefits not getting them, there will be a level of fraudulent claims, or:
2 - we eradicate fraudulent claims, but some genuine ones will also be turned down.

Assessing people is always going to rely to some extent on self-reporting. None of my specialists have a fucking clue how I actually live my life. They can suggest (if they've some imagination and of course many of them would not have) that for example, I'd get out of breath easily, struggle to stand for more than a few seconds, be unable to physically exert myself...

But to truly be able to describe HOW I live and cope, day to day, you need to be me.

If we move away from that, how, without throwing human rights and decency out the window, do we assess people? I don't see the government funding thousands of assessors who are all experts in multiple conditions, so...

Push them out of wheelchairs and see if they splat on the floor? Lob rocks at them to see if they lie there or get up and run away?

We're not that many steps away from lobbing folk in the village pond to see if they sink or float eh.

Dallidalli · 18/03/2025 22:31

PumpkinSoup21 · 18/03/2025 20:06

Here’s some food for thought - mental and physical health are linked. It’s a bit weird to imply that many people will turn out to be eeyore-ish gardeners who brighten up with a bit of fresh air or jolly administrators who are able to sit and focus on a screen all day.

First of, fresh air, sunlight and meaningful activities have been proven to aid mental health recovery or at least improve symptoms.
Second, as some with physical disabilities mentioned on this thread, having something like work tasks to focus on can distract from symptoms and again give meaning.

Not saying work 9-5 straight for all these groups but how about do work 1-2 hours a day with possibilities to increase hours while still on benefits so it gradually phases out ?

PickAChew · 18/03/2025 22:31

JustMovingUncomfortablySlow · 18/03/2025 20:59

"Wishy Washy set of symptoms?"

Jesus wept - I'll describe my "Wishy Washy" symptoms for you shall I? I'll start at the bottom.....

Feet swell up when I'm tired, in more pain than usual, or, just when they feel like it.

Pain either side of my Achilles Tendons - can't bear weight, pain is so excruciating on steps that I've taken to going downstairs on my bum.

I have pain either side of my shins which feels like someone is using a cheese grater up and down my tendons.

Left knee - tendon pain that feels like a knife stabbing if I bend it - but locks out if I don't move frequently.

Right thigh - sometimes left as well, feels like I've had 2 or 3 punches to the muscle. Agony when I wake up - sometimes takes me 20 minutes to get to a sitting position in the morning.

Left hip - pure bone ache - feels like an abscessed tooth but in my hip.

Lower back pain - standing for more than a few minutes leaves me in awful pain - goes quite quickly when I rest.

Left and right mid back - Dermatome pain - apparently feels like shingles (never had them). When it's bad, I can't have anything on my top half and have to lay in bed naked to the waist.

Chest - Costochondritis (that's inflammation of the cartilage that joins the upper ribs to the breastbone). First episode, I thought I was having a heart attack.

Neck/Shoulders - Top of my spine feels like I'm being stabbed with needles. Shoulders stiff and Left side swells up.

Bladder - when I need to go - I NEED to go. That's fun in the morning when my thigh hurts and I can't get out of bed. Pads help but I've been known to cough or sneeze and piss the entire bed, through the great big granny pad I'm embarrassingly forced to wear, because I can't move fast enough.

Bowels - IBS symptoms - that's fun too when I'm slow on my feet.

Brain Fog - Best I can describe this is word blindness - My son will ask if I want a cuppa and my answer will be "yes please love, can I have the one that isn't coffee" - because I can't remember the word for tea. I forgot the word for armchair earlier and called it "the thing you sit on that isn't a sofa".

Fatigue - Ever had newborn twins, with colic, that don't sleep and no one helps you? That's what Chronic Fatigue is like. It's not "a bit over tired". And guess what? It doesn't get better with sleep - I could sleep for 12 hours (I wish) and I'd be just as fatigued when I woke up.

Insomnia - Both pain based and well, just because my brain decides I don't have enough problems - this one is especially fun when I'm in pain - even with the sleepy meds. Happens every change of season, usually lasts about 6 weeks straight.

Vertigo and Tinnitus - OK, I've had these two since way before I started getting any Fibro symptoms - but Fibro makes them a hell of a lot worse. Upside of this is at least I know I'm not dying because I can hear my heartbeat in my left ear constantly.

I was a fit and healthy 40 something year old - now I'm fifty something, have to use a walking stick, can only go out with my mobility scooter and a trip to Tesco for a few bits can put me in bed for hours, if not days. For the last 48 hours I've been on a cycle of sleep for an hour, wake for two hours and I've only been out of bed to make a cuppa and pee. Everything hurts and all I want is a hot bath with Radox powder and Epsom Salts. Except I don't have enough energy to get out of my pj's and into the bath, soak, maybe wash, if I can reach around myself, and then get out, get dry and put clean jammies on. And it makes me cry, I can't do something as simple as that.

Spend a day with the kind of ongoing pain that I have - without any decent pain meds (because Opioids don't work for Fibro - and I would't want to take them long term anyway). Anti-depressants or anti-seizure meds are the only drugs advised for Fibro (apart from Ibuprofen) and neither of them work for me.

Now tell me about my fucking nice wishy washy set of symptoms, that can't be proved

Please don't ever feel you need to justify yourself to the myriad posters who are here to stir up hate. Flowers

Walkaround · 18/03/2025 22:32

Overtheatlantic · 18/03/2025 16:20

Care homes, local authorities and education institutions will offer more flexibility than regular corporate jobs.

🤣Sorry, but you have to be physically fit to look after people in care homes, reliable, able to work antisocial and long hours, and also emotionally robust. As for educational institutions - no way do educational institutions offer more flexibility than other places, certainly not for educating people aged 0-18. There is no flexibility whatsoever during term time, you have to turn up in person, not be prone to catching the multiple illnesses the children are bringing into school with them, and also be physically and emotionally robust and utterly, utterly reliable, or you become a massive drain on all your colleagues. You are caring for society’s most vulnerable, you aren’t supposed to be the vulnerable one. Local Authorities - have no money to obligingly employ lots of people with genuine disabilities. These have to be the stupidest examples of good places to employ people with disabilities that I’ve read.

WiddlinDiddlin · 18/03/2025 22:32

Dallidalli · 18/03/2025 22:31

First of, fresh air, sunlight and meaningful activities have been proven to aid mental health recovery or at least improve symptoms.
Second, as some with physical disabilities mentioned on this thread, having something like work tasks to focus on can distract from symptoms and again give meaning.

Not saying work 9-5 straight for all these groups but how about do work 1-2 hours a day with possibilities to increase hours while still on benefits so it gradually phases out ?

What work?

What work can be done by anyone, any educational and cognitive level, for 1 to 2 hours a few days a week.

What happens if one week they're not able to do their presumably piece-meal drudge work. Sanctions? Cut their money for that week?

TheFairyCaravan · 18/03/2025 22:33

JitterbugFairy · 18/03/2025 22:17

If that's the case,you wouldn't have your money stopped surely?

The mobility component isn’t being changed, it’s the daily living component. Hopefully mine won’t change. We don’t claim anything else because DH earns a very good wage, and has a military pension, so I wont be going to work. Regardless of that, I’m very angry at what the government has announced today. They are incredibly shortsighted and have forgotten that real people are at the end of this. People will die as a result, just like they did when the Tories changed DLA to PIP

DodoTired · 18/03/2025 22:34

Autisticunemployable · 18/03/2025 17:49

Within the space of 4.5 years (age 23 onwards) I developed coeliac disease and then crohns, hashimotos thyroiditis and type 1 diabetes
edited to add I also have endometriosis and adenomyosis but I don’t know if they are classed as autoimmune

Edited

Sorry these are preventing you from working??

PickAChew · 18/03/2025 22:34

Dallidalli · 18/03/2025 22:31

First of, fresh air, sunlight and meaningful activities have been proven to aid mental health recovery or at least improve symptoms.
Second, as some with physical disabilities mentioned on this thread, having something like work tasks to focus on can distract from symptoms and again give meaning.

Not saying work 9-5 straight for all these groups but how about do work 1-2 hours a day with possibilities to increase hours while still on benefits so it gradually phases out ?

That requires an employer who would be happy to take so one on on those terms, which is what this thread is about.

Thoughtsonstuff · 18/03/2025 22:35

WiddlinDiddlin · 18/03/2025 22:32

What work?

What work can be done by anyone, any educational and cognitive level, for 1 to 2 hours a few days a week.

What happens if one week they're not able to do their presumably piece-meal drudge work. Sanctions? Cut their money for that week?

Piecemeal drudge work? I'd take any job I could do, like anyone else who needs the money.

Dallidalli · 18/03/2025 22:39

WiddlinDiddlin · 18/03/2025 22:32

What work?

What work can be done by anyone, any educational and cognitive level, for 1 to 2 hours a few days a week.

What happens if one week they're not able to do their presumably piece-meal drudge work. Sanctions? Cut their money for that week?

I wish I had all the answers that's what is making this discussion actually important.
As I mentioned before, online tutoring or gardening depending on level of ability. When you sick you're getting sick pay.
Government needs to change rules around employment too in order for this to work

Puyyt · 18/03/2025 22:40

Thoughtsonstuff · 18/03/2025 22:35

Piecemeal drudge work? I'd take any job I could do, like anyone else who needs the money.

Because you're not disabled so you dont have any restrictions??

How is that so hard for you to understand?

HelenaWaiting · 18/03/2025 22:40

MrsBennetsPoorNerves · 18/03/2025 16:45

Perhaps some of the money saved from disability benefits needs to be spent on funds that would encourage employers to invest in disabled employees. Money to support reasonable adjustments, for example, or incentives for employers who offer flexible, sustainable, long term jobs to people who have been out of work for a long time.

Reasonable adjustments and investment in a diverse workforce are requirements of the Equality Act. The government shouldn't be bribing employers to comply with the law.

Kpo58 · 18/03/2025 22:42

Dallidalli · 18/03/2025 22:31

First of, fresh air, sunlight and meaningful activities have been proven to aid mental health recovery or at least improve symptoms.
Second, as some with physical disabilities mentioned on this thread, having something like work tasks to focus on can distract from symptoms and again give meaning.

Not saying work 9-5 straight for all these groups but how about do work 1-2 hours a day with possibilities to increase hours while still on benefits so it gradually phases out ?

That's going to be hard as in many places they are looking to build on pretty much any green space available, including grass verges. In some parts of London it's so built on, none of the flats have any green space outside of them and open up directly onto the street. It's feels pretty suffocating. I doubt that that type of environment is doing anyone's health any good and there won't be any outdoor menial jobs due to the lack of green space.

Dallidalli · 18/03/2025 22:44

PickAChew · 18/03/2025 22:34

That requires an employer who would be happy to take so one on on those terms, which is what this thread is about.

You are right and I agree rules around employment have to be more flexible for people. I just keep thinking about tutoring that would hit two birds with one stone and solve issues.

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