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Whole families on UC, PIP, DLA and carers' allowance for each other?

580 replies

Hutinthemiddleofnowhere · 05/09/2026 23:03

This isn't a bashing, rather a genuine observation and we're privileged in the UK to have support with benefits and disabilities.

Having adopted 2 siblings with special needs over a decade ago it opened me up to a whole new world to me. With DC in specialist schools and needing a lot of intervention from agencies and medical support I've met so many parents and children. As a teacher this was so insightful and, while having always been extra devoted to students who had difficulties, my own experience as a parent took it to another level.

Teaching, I was always aware and sympathetic to those who barely made it to lesson, almost fell asleep but professionally had to adhere to the 'not participating' and when told to 'fuck off' it was call out. I knew there would be further investigation as to why they act like this by more able and senior colleagues. Didn't take it personally but, as you can imagine, it's difficult when you have several students like this while under the pressure of teaching a tricky maths part of the syllabus.

So as a parent of ND DC I experienced it from the other side. It was very difficult because our DC were causing disruptions due to their severe diagnosis.

Throughout our journey and specialist schools I saw a lot of reality. This comes (finally) back to my point. Year after year it became blatantly obvious that the vast majority of children have parents with their own issues, whether hereditary or learnt behaviour.

I got a job at the primary school as a liason officer so met most parents. All lovely and care about their DC but sadly struggled with managing themselves, their homes etc. Those few who weren't eligible for taxis and escorts (walkable distance) relied heavily on GPs to take and pick up from school. There were some parents who did drive and drop off, like me, but it was about 5%.

So mostly the parents were on UC, claimed PIp for anxiety and MH, got DLA for all DC and also carers' allowance for looking after DC. While i visited it was clear they were were reclusive, their days were spent watching TV, gaming, DC picked up in a taxi and they had struggled to get out of bed, knew they are provided breakfast at school, went back to bed. Yes I've seen this on an early morning visit multiple times.

I understand but also a part of me felt frustrated that they had fallen into a rut, able bodied, could have long conversations, but have had so much support that has enabled this.

As a school we reached out to parents to come and integrate, provided workshops, held informal educational classes how we can help our DC. As a parent and before being employed there I attended these and it so nice to meet other parents. The reality... they just sat there, being served coffee by an already busy TA, talked all the way through the presentations then left, after already leaving several times for a smoke during an hour and half get together. Still as an attending parent at this point I could see TA was struggling so stepped in to help serve the refreshments, set up equipment and clear up afterwards. One Mum asked me to open a window, another asked to give her some biscuits...I was the same as them, a parent, but they were just totally oblivious to the situation.

Then walking out, having cleaned up and they were chatting outside, all I heard was that was so boring, I know how to bring up my kids, waste of time coming out, so what you doing now, probably Netflix.

Then getting the role and seeing deeper into their lifestyles it confirmed that actually so many of these parents had come from a generational cycle with low aspirations and no encouragement within modern education, social workers or support from us all could change their mindsets of behaviour. Sadly it really is a case of we get money, DC have their consoles, school provides meals and exercise, bags of amazing stuff at Christmas and end of year which we don't even say thank you for, we can complain online if we don't like something etc.

This is just the basic circumstances, delve deeper and you would be shocked at how some of these poor kids live. A whole different thread would have to be made about drug dealing, violence, not allowing DC in the house so they have to become one of the balaclava gangs and so much more.

As parents, even if we have our own issues, we all need to put our DC first, not rely on others to do it for us.

OP posts:
Thread gallery
5
Itchthescratch · Yesterday 12:02

LakieLady · Yesterday 11:52

One of my siblings actually said to me that she wouldn’t get out of bed as early as me for a salary. I thought she was stupid and far too comfortable on her benefits. Her £4,000 per month on benefits made her ignorant to the real world in terms of minimum wage and living in a budget. She has no rent or council tax to pay. She is comfortable in her little bubble. She has made 4 children who all have the same disability therefore PIP.

That's shocking, @Ethelspagetti. She should put them all in care and get a bloody job.

Oh, hang on ... Google tells me it costs around £6kpw to keep a child in care in the UK, so that would be far more costly than your sister getting £4k a month to care for them herself. She's saving the taxpayer a small fortune.

The logic here is mind blowing.

People that can't afford to have children having four with expensive SEN. Very few people have the resources to look after four children properly, let alone if they don't work and are disabled themselves. Surely she realised after the first two that her children have additional needs and it would be very difficult for her or the state to meet these needs, yet she selfishly continued having more and more children. She now never needs to work a day in her life, gets paid a small fortune in benefits and we are supposed to be grateful to her for looking after the children she chose to have? If we suggest otherwise then we get told she's saving the country millions.

All parents should look after their own children as default. We aren't all saving the state money. Whatever happend to personal responsibility and giving a shit about the conditions you are bringing your children into? I judge her, resent her and don't want her to financially benefit from her feckless decisions. I don't want her children to suffer. This is the paradox but I will never accept we should be grateful to her.

Spaniels4Eva · Yesterday 12:05

Claiming benefits should never give an equivalent or even better lifestyle than those of working people. We should be more focused on supporting the younger generation/working families on low incomes so they can have better childcare to work full time, and anyone too lazy/anxious to work should have to rely on family/friends to support their lifestyles like generations did 50 years ago.

itsgettingweird · Yesterday 12:16

NoelEdmondsHairGel · Yesterday 10:44

You are demonstrating my point.

Neither I nor the OP are talking about you.

Yet you jump in to derail the conversation. You are defending those who abuse the system. You are trying to prevent a discussion about how to help those who are stuck in a benefits rut and don’t want to get out of it because that is what their community does and all they know.

Your defensiveness is blinding you.

Because I don’t believe people do abuse the system.

No en masse like the OP says.

Im lucky that my upbringing was generally middle class and so k was raised in an aspirational household. I’m intelligent so did well at school and had a fairly ok school experience.

It gave me the tools I needed to cope and manage when things went tits up and unprepared in my adult life.

Some people aren’t that lucky .

Jaxhog · Yesterday 12:17

I think the point the Op is trying to make, is that the benefits system actually encourages some parents to coast without taking any responsibility for at least attempting to stop the cycle, yet they continue to bring new children into this cycle. It's pretty difficult for any child to be motivated to get out of a benefits cycle without parental and external support.

Of course this doesn't apply to all parents with difficult children, but don't kid yourselves, it does apply to a sizable minority.

Itchthescratch · Yesterday 12:24

itsgettingweird · Yesterday 12:16

Because I don’t believe people do abuse the system.

No en masse like the OP says.

Im lucky that my upbringing was generally middle class and so k was raised in an aspirational household. I’m intelligent so did well at school and had a fairly ok school experience.

It gave me the tools I needed to cope and manage when things went tits up and unprepared in my adult life.

Some people aren’t that lucky .

I grew up in a working/under class environment. People were absolutely abusing the system en masse even back then. It was an open secret and lots of girls aspired to have kids ASAP and get a council house knowing they wouldn't have to work for decades if they had enough children. Benefits have actually tightened quite a lot since then in terms of requiring parents to work. I think this is a factor in the increase in disability claims. Obviously not everybody and perhaps not even most, but don't kid yourself it isn't happening.
They probably weren't as lucky as you but lots of my friends with crap backgrounds have made something of themselves. It's not all about luck and it really undermines what some have achieved by pretending that it is.

likelysuspect · Yesterday 12:27

These threads always descend the same way. Posters take it personally and start rattling on about their personal circumstances defensively, listing condition after condition as evidence of why they dont fit what OP is talking about

Then people use examples of very extreme conditions/illnesses like the quadraplegic and make out people are expecting him to spring out of bed and do a days work on the bins or something

The very point is, those examples dont fit what OP is talking about, the observations are about a very large minority who conditions are fluid, vague, based on years of apathy, poor lifestyle, easy to manipulate.

The example above of the woman with anxiety is a good one, living a full life, yet posters are convinced 'there must be a lot more to the claim than you dont know about'. Im sure there is more to 'the claim', that doesnt mean there is more to her condition, the evidence is there in front of your eyes, living a full life, no doubt work or the thought of it brings on anxiety symptoms. That is not a reason to be paying someone in this situation.

And, just an observation on this thread, for the love of god, ASD/ND is not 'hereditary', the current working theory is that its genetic, they are not the same thing.

Ethelspagetti · Yesterday 12:27

LakieLady · Yesterday 11:52

One of my siblings actually said to me that she wouldn’t get out of bed as early as me for a salary. I thought she was stupid and far too comfortable on her benefits. Her £4,000 per month on benefits made her ignorant to the real world in terms of minimum wage and living in a budget. She has no rent or council tax to pay. She is comfortable in her little bubble. She has made 4 children who all have the same disability therefore PIP.

That's shocking, @Ethelspagetti. She should put them all in care and get a bloody job.

Oh, hang on ... Google tells me it costs around £6kpw to keep a child in care in the UK, so that would be far more costly than your sister getting £4k a month to care for them herself. She's saving the taxpayer a small fortune.

No it actually costs more because the government funds all 4 children with taxis to and from school. Three are at a local school but the eldest is at a private school near London, it is funded by Hull council. He gets a taxi there on Sundays and returns on Fridays, as it’s a boarding school. The specialist school is miles away and taxis charge the council! My sister is fighting for the next sibling to go there as it is better for her children. How is that fair??! This government are crazy and most people are ignorant to the facts, unless they see it for themselves. Obviously I don’t want anyone’s child to go
into care. I do frown upon extra tax payers money being thrown at them because they are disabled.

David15 · Yesterday 12:33

Hutinthemiddleofnowhere · 05/09/2026 23:03

This isn't a bashing, rather a genuine observation and we're privileged in the UK to have support with benefits and disabilities.

Having adopted 2 siblings with special needs over a decade ago it opened me up to a whole new world to me. With DC in specialist schools and needing a lot of intervention from agencies and medical support I've met so many parents and children. As a teacher this was so insightful and, while having always been extra devoted to students who had difficulties, my own experience as a parent took it to another level.

Teaching, I was always aware and sympathetic to those who barely made it to lesson, almost fell asleep but professionally had to adhere to the 'not participating' and when told to 'fuck off' it was call out. I knew there would be further investigation as to why they act like this by more able and senior colleagues. Didn't take it personally but, as you can imagine, it's difficult when you have several students like this while under the pressure of teaching a tricky maths part of the syllabus.

So as a parent of ND DC I experienced it from the other side. It was very difficult because our DC were causing disruptions due to their severe diagnosis.

Throughout our journey and specialist schools I saw a lot of reality. This comes (finally) back to my point. Year after year it became blatantly obvious that the vast majority of children have parents with their own issues, whether hereditary or learnt behaviour.

I got a job at the primary school as a liason officer so met most parents. All lovely and care about their DC but sadly struggled with managing themselves, their homes etc. Those few who weren't eligible for taxis and escorts (walkable distance) relied heavily on GPs to take and pick up from school. There were some parents who did drive and drop off, like me, but it was about 5%.

So mostly the parents were on UC, claimed PIp for anxiety and MH, got DLA for all DC and also carers' allowance for looking after DC. While i visited it was clear they were were reclusive, their days were spent watching TV, gaming, DC picked up in a taxi and they had struggled to get out of bed, knew they are provided breakfast at school, went back to bed. Yes I've seen this on an early morning visit multiple times.

I understand but also a part of me felt frustrated that they had fallen into a rut, able bodied, could have long conversations, but have had so much support that has enabled this.

As a school we reached out to parents to come and integrate, provided workshops, held informal educational classes how we can help our DC. As a parent and before being employed there I attended these and it so nice to meet other parents. The reality... they just sat there, being served coffee by an already busy TA, talked all the way through the presentations then left, after already leaving several times for a smoke during an hour and half get together. Still as an attending parent at this point I could see TA was struggling so stepped in to help serve the refreshments, set up equipment and clear up afterwards. One Mum asked me to open a window, another asked to give her some biscuits...I was the same as them, a parent, but they were just totally oblivious to the situation.

Then walking out, having cleaned up and they were chatting outside, all I heard was that was so boring, I know how to bring up my kids, waste of time coming out, so what you doing now, probably Netflix.

Then getting the role and seeing deeper into their lifestyles it confirmed that actually so many of these parents had come from a generational cycle with low aspirations and no encouragement within modern education, social workers or support from us all could change their mindsets of behaviour. Sadly it really is a case of we get money, DC have their consoles, school provides meals and exercise, bags of amazing stuff at Christmas and end of year which we don't even say thank you for, we can complain online if we don't like something etc.

This is just the basic circumstances, delve deeper and you would be shocked at how some of these poor kids live. A whole different thread would have to be made about drug dealing, violence, not allowing DC in the house so they have to become one of the balaclava gangs and so much more.

As parents, even if we have our own issues, we all need to put our DC first, not rely on others to do it for us.

I've an older child with SN who gets DLA, it gets spent on activities to help him with his development. My husband and I work, get up early and keep the house clean.

Itchthescratch · Yesterday 12:34

likelysuspect · Yesterday 12:27

These threads always descend the same way. Posters take it personally and start rattling on about their personal circumstances defensively, listing condition after condition as evidence of why they dont fit what OP is talking about

Then people use examples of very extreme conditions/illnesses like the quadraplegic and make out people are expecting him to spring out of bed and do a days work on the bins or something

The very point is, those examples dont fit what OP is talking about, the observations are about a very large minority who conditions are fluid, vague, based on years of apathy, poor lifestyle, easy to manipulate.

The example above of the woman with anxiety is a good one, living a full life, yet posters are convinced 'there must be a lot more to the claim than you dont know about'. Im sure there is more to 'the claim', that doesnt mean there is more to her condition, the evidence is there in front of your eyes, living a full life, no doubt work or the thought of it brings on anxiety symptoms. That is not a reason to be paying someone in this situation.

And, just an observation on this thread, for the love of god, ASD/ND is not 'hereditary', the current working theory is that its genetic, they are not the same thing.

Exactly, if I read a thread about lazy and entitled mothers, I don't assume it's about me because I'm a mother. I don't list all the ways I'm not entitled or lazy as if someone has personally accused me. I certainly don't suggest that mothers can never be lazy or entitled just because I think I'm not. The willingness of some posters to go out there to bat for other people that they know nothing about is alarming. Especially when by doing this they are potentially defending and denying situations that are actively harming children. Defending these terrible parents is diabolical

cornflakecrunchie · Yesterday 12:36

Hmm, what to say without it being outing.. shall we say I know of someone claiming for a child but no-one but them apparently sees symptoms, inc school.. brand new car (Motability) & loft stuffed with (unused) wheelchairs etc..
If there's one person doing this, there's many more.

On the other hand, I had to do a Parenting course for my youngest, despite bringing others up successfully.. my child was eventually diagnosed ASD! In fact I can go back much further than that, to my eldest who had colic as a baby. The Health Visitor (somewhere near God to me, as a young mum) told me to use less formula & more water in his feeds, which would help. I talked to another mum in the clinic & she confirmed she'd been told the same, until her husband had put his foot down & said not only did their baby have colic, she was hungry too.. we both mentioned this to the doctor who insisted a Health Visitor wouldn't have said that & we must have misunderstood..

It is hard to see wrongdoing & people scamming the system.
Some parents ARE thick, tbh, BUT have a level of cunning, to take & take. But some of the courses, meetings etc ARE boring & treat adults like children. Unfortunately I don't know the answer.

x2boys · Yesterday 12:40

likelysuspect · Yesterday 12:27

These threads always descend the same way. Posters take it personally and start rattling on about their personal circumstances defensively, listing condition after condition as evidence of why they dont fit what OP is talking about

Then people use examples of very extreme conditions/illnesses like the quadraplegic and make out people are expecting him to spring out of bed and do a days work on the bins or something

The very point is, those examples dont fit what OP is talking about, the observations are about a very large minority who conditions are fluid, vague, based on years of apathy, poor lifestyle, easy to manipulate.

The example above of the woman with anxiety is a good one, living a full life, yet posters are convinced 'there must be a lot more to the claim than you dont know about'. Im sure there is more to 'the claim', that doesnt mean there is more to her condition, the evidence is there in front of your eyes, living a full life, no doubt work or the thought of it brings on anxiety symptoms. That is not a reason to be paying someone in this situation.

And, just an observation on this thread, for the love of god, ASD/ND is not 'hereditary', the current working theory is that its genetic, they are not the same thing.

Some of the extreme examples are because one poster suggested peoole on PIP should do community work for it
Later she changed it to not everyone
But the intiial generlisation doesnt help
Im with you with the genetic/ hereiditry thing
My son has a a rare chromosome disorder thought to be the underlying reaon for his autism and learning disabillities whilst they can be inherited from a parent it was De novo in his case
So yes its genetic but not inherited.

Beepen · Yesterday 12:47

Itchthescratch · Yesterday 12:34

Exactly, if I read a thread about lazy and entitled mothers, I don't assume it's about me because I'm a mother. I don't list all the ways I'm not entitled or lazy as if someone has personally accused me. I certainly don't suggest that mothers can never be lazy or entitled just because I think I'm not. The willingness of some posters to go out there to bat for other people that they know nothing about is alarming. Especially when by doing this they are potentially defending and denying situations that are actively harming children. Defending these terrible parents is diabolical

Exactly this
And there's always an assumption that working people/people who don't came benefits are Neurotypical and full of health and vitality with no MH issues

If you are being honest on a PIP application and you are successful then you must be far too disabled to care for someone else with disabilities

Kirbert2 · Yesterday 12:49

ElefantAndCastle · Yesterday 09:29

I would rather that UK paid for these services than forking more or less random out.

It seems to work a lot better in other countries not to have all these paid family members. One benefit would also be useful to hand out. My native country it's a benefit a bot more than minimum wages. Not a open pot of money. At all.
No pip no extra money for being your partner's or mum's carer. No first to council housing. Not all that fuss.

How is accessible housing dealt with in your native country? The only way I was able to access a house suitable for my disabled son was through the council.

emuloc · Yesterday 12:50

Hmm, what to say without it being outing.. shall we say I know of someone claiming for a child but no-one but them apparently sees symptoms, inc school.. brand new car (Motability) & loft stuffed with (unused) wheelchairs etc..
If there's one person doing this, there's many more.

A loft stuffed with unused wheelchairs! Were these wheelchairs purchased by the Mother, or prescribed by the NHS? How would you know what the school is witnessing?

x2boys · Yesterday 12:54

cornflakecrunchie · Yesterday 12:36

Hmm, what to say without it being outing.. shall we say I know of someone claiming for a child but no-one but them apparently sees symptoms, inc school.. brand new car (Motability) & loft stuffed with (unused) wheelchairs etc..
If there's one person doing this, there's many more.

On the other hand, I had to do a Parenting course for my youngest, despite bringing others up successfully.. my child was eventually diagnosed ASD! In fact I can go back much further than that, to my eldest who had colic as a baby. The Health Visitor (somewhere near God to me, as a young mum) told me to use less formula & more water in his feeds, which would help. I talked to another mum in the clinic & she confirmed she'd been told the same, until her husband had put his foot down & said not only did their baby have colic, she was hungry too.. we both mentioned this to the doctor who insisted a Health Visitor wouldn't have said that & we must have misunderstood..

It is hard to see wrongdoing & people scamming the system.
Some parents ARE thick, tbh, BUT have a level of cunning, to take & take. But some of the courses, meetings etc ARE boring & treat adults like children. Unfortunately I don't know the answer.

You are talking bollocks
To get High rate mobility under DLA the child either wont be able to walk at all
Be blind
Be blind and deaf
Have no feet or limbs
Have a condtion that means that walking severly impairs their health
Be virtually unable to walk ( this can include severe challenging behaviour that makes walking any where safely extremely difficult
Or severe mental impairment
My son got it under severe mental impairment i had to go to tribunal for it
He goes to a specisl school for children with severe and profound learning disabillties its blindingly obvious to everyone hes severly mentally impaired
Nobody gets HRM
On just the say so of the parent.

ExpectMore · Yesterday 12:55

DrBlackbird · Yesterday 08:23

As@JLou08 says Do you not realise that those parents you're referring to are more likely to have their own learning difficulties/ND which makes it difficult for them to engage with training and impacts their executive function? I'm sure most of them are doing all they can for their DC but they don't all have the same level of capabilities that you do.

I would guarantee that all these parents will have undiagnosed SENs/NB. And I know in-generational families on benefits. From the outside what we see are people who live limited lives, eat unhealthily, spend money they don’t have getting into debt, and too much time on technology.

But before you cut their benefits @Hutinthemiddleofnowhere driving them further into poverty, and as you’re a teacher, why not campaign for better education that meets the needs of children with Sen? An education system that would enable them to not only get an education, but experience one that hasn’t destroyed all vestiges of self belief when they got their weekly spelling tests wrong week after week or couldn’t perform their fast paced mental maths in front of the whole class. Where art, music, drama, industrial design wasn’t removed from schools or school fields sold off to enable students to succeed in other areas.

Why not support political parties that will stand up to the tech bros who have deliberately designed technology that is addictive, destroys young girls self esteem, and exposes everyone to the worst of humanity all in the name of obscene profits? Why not campaign against a food industry that has deliberately engineered calorie dense HPF with salt/sugar/fat combined to give dopamine hits and which is cheaper than fresh food? Why not campaign against the firms that have off shored the well paying jobs that required skills but not a degree in theoretical physics or campaign against betting firms using sophisticated marketing techniques to encourage problem betting? Did you argue against the ridiculous white elephant of HS2 sucking up £100 billion that could’ve been spent on so many better projects? Fight to highlight the corruption and waste of our taxpayer money going to friends in every political party (none is immune)?

Lift your head up op and instead of focusing on the families, look at our wider society and our economy that has slipped from benefiting a majority to creating wealth for a few. I don’t know what the answer is because the welfare bill is likely unsustainable but thanks again to technology, the remaining jobs can be done with fewer people and will be highly work intensive. Not suitable for those with MH problems or physical ailments or those with undiagnosed and unsupported SENs.

This trajectory has been allowed for decades now, no government has seemingly been able or had the will to address the issues given the need to rely on private donations. The evidence against cryptocurrencies is dire with its negative consequences for society but if Reform got elected, then we’d see that brought in to further damage our economy and society.

What we so desperately need is for all our politicians and our business elites to actually want to serve the whole country instead of themselves, their party, their business mates. Let’s hope Burnham’s cabinet can create miracles though I’m not holding my breath. More taxes, but same problems.

All this campaigning @DrBlackbird at everybody else whose fault it is, wouldn’t it be better if everyone just took some personal responsibility and accountability for their own lives and that of their children and loved ones?

it’s not always the big bad systems fault. Sometimes the issue is staring at us from the mirror and rather than waste energy blaming the others, we’d be better off just getting on with it.

The issue with doing so of course is that once you accept it’s nobody else’s fault, there’s only one person to blame….

Kirbert2 · Yesterday 12:56

emuloc · Yesterday 12:50

Hmm, what to say without it being outing.. shall we say I know of someone claiming for a child but no-one but them apparently sees symptoms, inc school.. brand new car (Motability) & loft stuffed with (unused) wheelchairs etc..
If there's one person doing this, there's many more.

A loft stuffed with unused wheelchairs! Were these wheelchairs purchased by the Mother, or prescribed by the NHS? How would you know what the school is witnessing?

and if they were referred to by wheelchair services, please can you tell me which area because I'd love to know which wheelchair services hands out wheelchairs like sweeties!

BadBadCat · Yesterday 12:57

DontBuyAnotherBook · Yesterday 11:49

I want to claim as I wear hearing aids in both ears but I work and even though I still struggle to hear customers it will probably be a nope.

How will the PIP money help you?

cornflakecrunchie · Yesterday 12:58

@x2boys I can't be too outing but the child isn't the only one they are claiming for.. (Re the car.)

Shardonneigghhh · Yesterday 13:07

The problem in my experience is that your child gets a diagnosis and then is discharged from the service. The onus is on the school to support the parents. Often the school is not the right one and you spend years fighting the system to get the right one. Any "support" from the school assumes you don't work at puts the sessions on during the school day, so still there is no support. You take the day off to attend at grt shown a powerpoint which patronises you by explaining that giving your kid Monster before bed will affect their sleep. Yet when you advocate for your child, the school staff send emails to each other slating you and calling you "Persistent" (true story, i was accidentally cc'd in).
Diagnosis, no support. Every one assumes you don't work. School staff judge you regardless of whether you work or not.

Makkka · Yesterday 13:22

x2boys · Yesterday 12:54

You are talking bollocks
To get High rate mobility under DLA the child either wont be able to walk at all
Be blind
Be blind and deaf
Have no feet or limbs
Have a condtion that means that walking severly impairs their health
Be virtually unable to walk ( this can include severe challenging behaviour that makes walking any where safely extremely difficult
Or severe mental impairment
My son got it under severe mental impairment i had to go to tribunal for it
He goes to a specisl school for children with severe and profound learning disabillties its blindingly obvious to everyone hes severly mentally impaired
Nobody gets HRM
On just the say so of the parent.

I agree.

I also think a lot of people on here are talking bollocks and are just trying to cause resentment. People will always play the system across the board and it does seem the new MH card is the old bad back, however some on here are making out PIP and DLA are easy to get and absolutely aren’t unless someone is telling big fat lies.
As you say, to get higher rate is extremely difficult.

plasticplate · Yesterday 13:34

OonaStubbs · Yesterday 01:34

Benefits are the worst thing that ever happened to this country, and I know I'll get called all the names under the sun for saying that but it's true. It's created a sense of learned helplessness and entitlement amongst so many people that is going to be very hard to eradicate.

What are you proposing instead for those that will never be able to work ? The workhouse, asylums or the final solution?

Makkka · Yesterday 13:38

plasticplate · Yesterday 13:34

What are you proposing instead for those that will never be able to work ? The workhouse, asylums or the final solution?

Exactly. The poster is clearly in the mindset of it’s not happening to me so I don’t care. They would do well to remember that we don’t know what’s around the comer and anyone of us could end up bed bound next week, including them.

x2boys · Yesterday 13:42

plasticplate · Yesterday 13:34

What are you proposing instead for those that will never be able to work ? The workhouse, asylums or the final solution?

Well on another thread
People were seriously euthanasia
And another one the Op thought it would be far cheaper for children with severe disabillties to be cared for in some kind of institution
Nevermind that they would in many cases be ripped away from loving families.

Harry12345 · Yesterday 13:44

SkinnyCigarette · Yesterday 02:47

Quit your job and claim benefits then.

No id rather keep going until I can’t any longer

Swipe left for the next trending thread