Monday, 26 October 2015

Sara’s teaching programme for the 1st year students University Of Wolverhampton Walsall Campus.



https://youtu.be/9qkk4QY4bes


What we have we done what do we need to?
Due to half term I guess you won’t be studying a lot at the moment but not to worry, you don’t have to and no rush and it's half term. I wouldn't except you to study all the time but when you do, I have written down in the teaching programme what is a head us next so if you do have chance please prepare yourself, if not not to worry to we can all help each other as a group when the time comes. I understand you could be on placement as well. I am just letting know about the sessions we and have done and the sessions I plain to come. I will put this report in an email to Lynne which she should get after half term, I guess soon as she’s aware of it she will make you aware too.

Like I said I know you guys are Student Learning Disability nurses but the idea of you learning these topics, is the awareness of how everyday issues can have affect on the health of people with disabilities and health problems.  

As for the that report about the Jobcentre and that, there's no stress,  pres sager or time limit when you study it. It's just some update information of what people with disabilities and health problems are facing with benefits, support and employment theses days. I can't promise but maybe a session could be planned where we could do some work on that a piece of work. Ever so often we will do a bit of revision on each topic. 

Session 1 I introduced myself and a short bit of information of what I will be teaching, which was. What are learning disabilities and health problems? What kind of disabilities and health problems are there? Communication and Accessible information.

  Second session. We did your first module was on the 23rd September 2015. You introduced yourselves to me, Lynne, each other and we introduced ourselves . I spoke to you about PCP Person Centered planning how that works, the balance between support and independence. You told me different forms of communication, which I listed down on the board. I can’t say when but I hope to do a session where we go through what disabilities and health problems there are and how different  people communicate with these disabilities and health problems. Very well done for what you have all done so far.


3rd session.  was the Benefit cuts 21st October 2015, just a little bit of reference advice. I can understand this reference could be very hard to get hold of but if you can get hold of it, there’s a lot of useful information, I don't except to look at it all the time but a bit of a time and learn as much as what you can before it goes out of date if you do get access to it. It’s the Disability Rights Handbook, I never thought about it until my sister bought me a copy for my birthday. I can understand as far as buying is concerned it may be too pricey and the same to download it as well. You may be able to get a copy from the library, which may better because it’s only dated from the April 2015 to April 2016. It’s according whether or not the libraries have a copy. You may able to ask even if the University library if there's a copy there.  I don’t want to keep on teaching the benefit cuts every session I do at the University but I may be able to ask Lynne if I could photocopy a page ever so often before the book goes out of date then we can do a bit of work on it or get a copy each for you. WWW.disabilityrightsuk.org

Well done for all of who took part in the Benefit’s cut session, everyone did very well indeed thank you.


Session 4 is to come. Different types of disabilities and health problems.
·       What are learning disabilities and health problems?
·       What kind of disabilities and health problems are there?  
·       How do disabilities and health problems start?
·       What can cause disabilities and health problems?
·       WWW.mencap.org.uk  for learning disabilities.
·       Tap your search engine in Mind, Rethink or and Healthy Mind for health problems. 


  • I forgot to add to the first and second session is to find out how much difference there is if any between learning disabilities and learning difficulties.
  • If there's time in the next session we may do some work on PCP Person Centered Planning if not we can plan it for another session.

Session 5.  (Accessible information easy read.)


More sessions are to be planned from there. I will also ask Lynne to forward this report in an email to Steven and Mick to share with the 3rd year and for Lynne to share it with the 2nd year too. 

Here is an aware of the lack of support disabled people are now getting with employment and that.
More jobcentre recordings: We can’t help disabled claimants at this jobcentre. You’ll have to go elsewhere
Posted on October 26, 2015
Here’s a very recent example of the extraordinary lack of support that disabled JSA claimants can find at jobcentres when they’re looking work.
In the recording below, an adviser at a north London jobcentre actually tells me that advisers at this jobcentre can’t give extra job search help or support to the disabled claimant who I’m with. The adviser doesn’t try to pretend otherwise. He says that the jobcentre can’t help this disabled man, because there are no Disability Employment Advisers at this jobcentre now (DEAs are advisers who are meant to have additional skills and time for disabled benefit claimants). Nobody else at the jobcentre can give the man extra support. The adviser said that the man’s only choice was to move jobcentres to one that does still have specialist disability advisers. That was the end of that. So much, I thought, for the DWP’s claims to me by recent email that disabled benefit claimants can expect “tailored support specific to their individual needs,” at jobcentres. These DWP claims of “tailored support” for disabled JSA claimants are rot as far as I’m concerned – as great a lie as the DWP’s use of fake benefit claimants and quotes in leaflets. It seems to me that when the DWP talks about “tailored support” for disabled claimants at jobcentres, the DWP pretends to offer a service that it does not.
The disabled JSA claimant in this case is a 52-year-old man who has learning and literacy difficulties. He worked for years as a kitchen and general assistant, but hasn’t found work since he was made redundant from his last job about six years ago. I’ve attended his JSA sign on sessions with him for over a year (we both wonder why we still bother a lot of the time). This man struggles with writing and spelling in particular. We’ve spent much time filling in job applications together. Here’s an example of an application form he filled in where he copied words that I wrote in my notebook into the form. You can see the trouble that he has writing coherent sentences even when he copies text:
This man often says that he is keen for a job. He says that he attends job fairs and when we met last week, we arranged to meet again to fill in application forms for porter and general assistant roles (he can’t use a computer, so needs other people to make online applications). He needs help to fill in the forms. He says that he’s lost his chance at jobs in the past, because he couldn’t complete forms to an acceptable standard: “I went to a nursing home in Enfield which I really should have got in there, because it was just a simple kitchen assistant job. No – the reason they give me was Oh, there were some mistakes in the application form and the spelling.”
That’s why at this man’s JSA sign on meeting last week, I asked the jobcentre adviser if anyone at the jobcentre could help this guy fill in his forms. The adviser said No, nobody could. The reason given? – this jobcentre no longer had a Disability Employment Adviser to provide that sort of support, as I say. The DEA left a few months ago, wasn’t replaced and nobody had taken on the extra duties. (The now-departed DEA at this jobcentre told me earlier this year that nobody else at the jobcentre would have time to help disabled claimants when she left). The jobcentre’s advice for this man was that he should move jobcentres, to Tottenham, if he wanted any help. There were still two DEAs working at the Tottenham jobcentre. And… that was it. I was sitting there thinking – great. Iain Duncan Smith wants to force more sick or disabled people onto job-seekers’ allowance and this is his idea of tailored job search support – a sad shrug from a jobcentre adviser and an instruction to go elsewhere:
Recording:
Transcript:
Me – “is there any facility like now that [DEA name removed] is gone for someone to help with an application? I mean I’m quite happy to help, but I just wondered if the jobcentre offered that kind of service… [to help with] the writing… this kind of stuff…
C – we don’t have ….that’s what I was explaining to him [the claimant], I don’t know if he was here with you, that before leaving [DEA name removed] knew that there would be no one to take over. She told me that she was advising him to go back to the Tottenham jobcentre, because Tottenham they have two [DEAs]
M – Yeah, he just has trouble getting there. So here they don’t, really, basically.”
A couple of things here.
The first thing is that moving jobcentres can be very difficult for someone who needs some support and finds change very hard to cope with. This man had already moved jobcentres from Kilburn when he was rehoused earlier this year. He hasn’t coped well with the move. He’s often angry and belligerent. Another move to another jobcentre would not be easy. He resists the idea absolutely. God only knows if he’d have to move again at some point, as well. The adviser we saw last week said that he expected the number of DEAs to drop across jobcentres, too – “to save money,” he said. Appointments at jobcentres already get cancelled because of a lack of staff. I have turned up for a number of jobcentre or work programme meetings over the past year, only to find that they’ve been cancelled due to a staff shortage. I can’t imagine this situation or the numbers improving.
The second point I’d make is that Disability Employment Advisers aren’t always brilliantly helpful anyway. I’m not convinced that “tailored support” for sick or disabled people is their exact goal. I think that their focus is governments: to push everybody into unpaid or very low-paid work. The DEAs I’ve met seem obsessed with pushing disabled people into unpaid work, or with lining disabled people up for the work programme and low-paid work choice jobs. Earlier this year, this man and I met several times with the DEA who recently departed this jobcentre. She ignored this man’s concerns about his diabetic illness ( you can hear a recording here ) and spent our meetings trying to sign this guy up for voluntary work, or for work choice programmes with Seetec. She didn’t fill in applications forms either, just by the way. She pushed reams of forms over the desk and expected me to talk the guy into agreeing to sign up for work choice, and, presumably, to fill in the forms if he did agree. There was nothing tailored going on there.
You see my point. Our fortnightly visits to the jobcentre are utterly hopeless. I’ve introduced a post-sign on lunch at Wetherspoons into the outing just so that we have something to look forward to and can chat like human beings. I’m guessing that this guy has been parked by the jobcentre in some way: he’s been unemployed for a long time, he’s getting older and he isn’t well (he has trouble with his diabetes and seems to struggle to manage his sugar levels). He has become very defensive and resistant as time has dragged on. I’d say that his various jobcentres have stuck him on some sort of Too Hard to Fix list. It may also be that decent advisers don’t want to torture him any more than they have to. It seems likely these people know full well that his only real options outside the jobcentre are unpaid work, or very low-paid, insecure, manual jobs. That being the case, they sign him on and let him go. And so on we go with the charade: backwards and forwards we travel to that jobcentre. We sit, see the jobcentre adviser and get that week’s job search signed off. Occasionally, an adviser makes noises about the work programme. We hear those noises and then we leave. I suppose that sooner or later, someone will force him onto another work programme course (he’s been on four).
I keep trying to work out what is really going on here. This guy is older and unwell, and now he’s belligerent. The jobcentre is just a place that guys in his situation are dumped these days. I expect he’ll soon be joined by plenty more people in similar situations. I already talk with other people in similar situations. As I say, Iain Duncan Smith plans to push more disabled people off disability benefits and onto job seekers’ allowance as people are expected to find work. His department claims that all will be well, because jobcentres are geared up to provide the support that sick or disabled people need to find decent work. That DWP email again: “Job seekers now have access to dedicated work coaches, who are trained to provide tailored support specific to their individual needs.” I’m saying I Think Not. This service isn’t tailored. It’s threadbare. There’s a disabled woman I attend another London jobcentre with: we’ve turned up twice to scheduled meetings with a work coach this year only to be told at the door that the work coach couldn’t make it.
It is high time that the DWP and work programme providers gave us some transparency with this “system.” Reporters should be given free access to work programme and work choice placements, and jobcentres. Let’s see what this tailored support really looks like all over. If Iain Duncan Smith is really going to shove more sick or disabled people into jobcentres, they will need something better than this. I can’t imagine that they’ll get it.

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This entry was posted in Public spending cuts, Welfare reform by Kate B. Bookmark the permalink.

13 THOUGHTS ON “MORE JOBCENTRE RECORDINGS: WE CAN’T HELP DISABLED CLAIMANTS AT THIS JOBCENTRE. YOU’LL HAVE TO GO ELSEWHERE”

1.   Dino on October 26, 2015 at 15:46 said:
When I lived near Leeds I used to shop in Castle ford and passed a job center on the way to ALDI, this wasn’t the job center I had to sign on at the one I signed on at was 9.2 miles from my home this one was just over 4 miles away, 4.4 to be exact, when I queried it with them they said that Here is an aware of the lack of support disabled people are now getting with employment and that.
More jobcentre recordings: We can’t help disabled claimants at this jobcentre. You’ll have to go elsewhere
Posted on October 26, 2015
Here’s a very recent example of the extraordinary lack of support that disabled JSA claimants can find at jobcentres when they’re looking work.
In the recording below, an adviser at a north London jobcentre actually tells me that advisers at this jobcentre can’t give extra job search help or support to the disabled claimant who I’m with. The adviser doesn’t try to pretend otherwise. He says that the jobcentre can’t help this disabled man, because there are no Disability Employment Advisers at this jobcentre now (DEAs are advisers who are meant to have additional skills and time for disabled benefit claimants). Nobody else at the jobcentre can give the man extra support. The adviser said that the man’s only choice was to move jobcentres to one that does still have specialist disability advisers. That was the end of that. So much, I thought, for the DWP’s claims to me by recent email that disabled benefit claimants can expect “tailored support specific to their individual needs,” at jobcentres. These DWP claims of “tailored support” for disabled JSA claimants are rot as far as I’m concerned – as great a lie as the DWP’s use of fake benefit claimants and quotes in leaflets. It seems to me that when the DWP talks about “tailored support” for disabled claimants at jobcentres, the DWP pretends to offer a service that it does not.
The disabled JSA claimant in this case is a 52-year-old man who has learning and literacy difficulties. He worked for years as a kitchen and general assistant, but hasn’t found work since he was made redundant from his last job about six years ago. I’ve attended his JSA sign on sessions with him for over a year (we both wonder why we still bother a lot of the time). This man struggles with writing and spelling in particular. We’ve spent much time filling in job applications together. Here’s an example of an application form he filled in where he copied words that I wrote in my notebook into the form. You can see the trouble that he has writing coherent sentences even when he copies text:
This man often says that he is keen for a job. He says that he attends job fairs and when we met last week, we arranged to meet again to fill in application forms for porter and general assistant roles (he can’t use a computer, so needs other people to make online applications). He needs help to fill in the forms. He says that he’s lost his chance at jobs in the past, because he couldn’t complete forms to an acceptable standard: “I went to a nursing home in Enfield which I really should have got in there, because it was just a simple kitchen assistant job. No – the reason they give me was Oh, there were some mistakes in the application form and the spelling.”
That’s why at this man’s JSA sign on meeting last week, I asked the jobcentre adviser if anyone at the jobcentre could help this guy fill in his forms. The adviser said No, nobody could. The reason given? – this jobcentre no longer had a Disability Employment Adviser to provide that sort of support, as I say. The DEA left a few months ago, wasn’t replaced and nobody had taken on the extra duties. (The now-departed DEA at this jobcentre told me earlier this year that nobody else at the jobcentre would have time to help disabled claimants when she left). The jobcentre’s advice for this man was that he should move jobcentres, to Tottenham, if he wanted any help. There were still two DEAs working at the Tottenham jobcentre. And… that was it. I was sitting there thinking – great. Iain Duncan Smith wants to force more sick or disabled people onto jobseekers’ allowance and this is his idea of tailored job search support – a sad shrug from a jobcentre adviser and an instruction to go elsewhere:
Recording:
Transcript:
Me – “is there any facility like now that [DEA name removed] is gone for someone to help with an application? I mean I’m quite happy to help, but I just wondered if the jobcentre offered that kind of service… [to help with] the writing… this kind of stuff…
C – we don’t have ….that’s what I was explaining to him [the claimant], I don’t know if he was here with you, that before leaving [DEA name removed] knew that there would be no one to take over. She told me that she was advising him to go back to the Tottenham jobcentre, because Tottenham they have two [DEAs]
M – Yeah, he just has trouble getting there. So here they don’t, really, basically.”
A couple of things here.
The first thing is that moving jobcentres can be very difficult for someone who needs some support and finds change very hard to cope with. This man had already moved jobcentres from Kilburn when he was rehoused earlier this year. He hasn’t coped well with the move. He’s often angry and belligerent. Another move to another jobcentre would not be easy. He resists the idea absolutely. God only knows if he’d have to move again at some point, as well. The adviser we saw last week said that he expected the number of DEAs to drop across jobcentres, too – “to save money,” he said. Appointments at jobcentres already get cancelled because of a lack of staff. I have turned up for a number of jobcentre or work programme meetings over the past year, only to find that they’ve been cancelled due to a staff shortage. I can’t imagine this situation or the numbers improving.
The second point I’d make is that Disability Employment Advisers aren’t always brilliantly helpful anyway. I’m not convinced that “tailored support” for sick or disabled people is their exact goal. I think that their focus is governments: to push everybody into unpaid or very low-paid work. The DEAs I’ve met seem obsessed with pushing disabled people into unpaid work, or with lining disabled people up for the work programme and low-paid work choice jobs. Earlier this year, this man and I met several times with the DEA who recently departed this jobcentre. She ignored this man’s concerns about his diabetic illness ( you can hear a recording here ) and spent our meetings trying to sign this guy up for voluntary work, or for work choice programmes with Seetec. She didn’t fill in applications forms either, just by the way. She pushed reams of forms over the desk and expected me to talk the guy into agreeing to sign up for work choice, and, presumably, to fill in the forms if he did agree. There was nothing tailored going on there.
You see my point. Our fortnightly visits to the jobcentre are utterly hopeless. I’ve introduced a post-sign on lunch at Wetherspoons into the outing just so that we have something to look forward to and can chat like human beings. I’m guessing that this guy has been parked by the jobcentre in some way: he’s been unemployed for a long time, he’s getting older and he isn’t well (he has trouble with his diabetes and seems to struggle to manage his sugar levels). He has become very defensive and resistant as time has dragged on. I’d say that his various jobcentres have stuck him on some sort of Too Hard to Fix list. It may also be that decent advisers don’t want to torture him any more than they have to. It seems likely these people know full well that his only real options outside the jobcentre are unpaid work, or very low-paid, insecure, manual jobs. That being the case, they sign him on and let him go. And so on we go with the charade: backwards and forwards we travel to that jobcentre. We sit, see the jobcentre adviser and get that week’s job search signed off. Occasionally, an adviser makes noises about the work programme. We hear those noises and then we leave. I suppose that sooner or later, someone will force him onto another work programme course (he’s been on four).
I keep trying to work out what is really going on here. This guy is older and unwell, and now he’s belligerent. The jobcentre is just a place that guys in his situation are dumped these days. I expect he’ll soon be joined by plenty more people in similar situations. I already talk with other people in similar situations. As I say, Iain Duncan Smith plans to push more disabled people off disability benefits and onto job seekers’ allowance as people are expected to find work. His department claims that all will be well, because jobcentres are geared up to provide the support that sick or disabled people need to find decent work. That DWP email again: “Job seekers now have access to dedicated work coaches, who are trained to provide tailored support specific to their individual needs.” I’m saying I Think Not. This service isn’t tailored. It’s threadbare. There’s a disabled woman I attend another London jobcentre with: we’ve turned up twice to scheduled meetings with a work coach this year only to be told at the door that the work coach couldn’t make it.
It is high time that the DWP and work programme providers gave us some transparency with this “system.” Reporters should be given free access to work programme and work choice placements, and jobcentres. Let’s see what this tailored support really looks like all over. If Iain Duncan Smith is really going to shove more sick or disabled people into jobcentres, they will need something better than this. I can’t imagine that they’ll get it.

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This entry was posted in Public spending cuts, Welfare reform by Kate B. Bookmark the permalink.

13 THOUGHTS ON “MORE JOBCENTRE RECORDINGS: WE CAN’T HELP DISABLED CLAIMANTS AT THIS JOBCENTRE. YOU’LL HAVE TO GO ELSEWHERE”

1.   Dino on October 26, 2015 at 15:46 said:
When I lived near Leeds I used to shop in Castle ford and passed a job center on the way to ALDI, this wasn’t the job center I had to sign on at the one I signed on at was 9.2 miles from my home this one was just over 4 miles away, 4.4 to be exact, when I queried it with them they said that JC+ was not in my area.
Re “tailored support specific to [our] individual needs”: Disability Equality Trainer M T has advised that the word ‘requirements’ is more powerful than ‘needs’. ‘Needs’ is a word too much linked to ‘neediness’, whereas ‘requirements suggest rights, responsibilities and authority.
And “tailored support” presupposes proper assessment of what our disabilities really involve. Proper assessment in itself would involve substantial up-front investment. The Wechsler Adult Intelligence Scale tests I went through with Camden Learning Disability Services near my 60th birthday indicate that for some intellectual functioning categories, my scores are ‘borderline’ on ‘learning disability’ range that is set at or below IQ score of 70. The subsequent report from CLDS gives me great documentation for ESA ‘Work Capability Assessment’ purposes, but no entitlement to even a formal diagnosis from CLDS that would formally diagnose my impairment/disability as dyspraxia.
Such a formal diagnosis, I am told, would cost me hundreds of pounds. So in effect, all the learning-and-co-learning hoops and hurdles I have gone through over the decades since 1978 when a Manpower Services Commission-run ‘Employment Rehabilitation Center's ‘Occupational Psychologist’ [sic] told me that my career difficulties stemmed from “a birth defect” have befitted me nothing in terms of employment credit.
Right wing ‘welfare reform’ is not really about rewarding effort and ‘saving disabled people from worthlessness’, but the privatization of the welfare state and screwing the economically vulnerable. Benefit sanctions and threat of sanctions are really a means of unconscionable global corporations finding commercial profit in exploiting the people they would previously have ‘parked’ as not worth the current time of day.
 JC+ was not in my area.
Re “tailored support specific to [our] individual needs”: Disability Equality Trainer M T has advised that the word ‘requirements’ is more powerful than ‘needs’. ‘Needs’ is a word too much linked to ‘neediness’, whereas ‘requirements suggest rights, responsibilities and authority.
And “tailored support” presupposes proper assessment of what our disabilities really involve. Proper assessment in itself would involve substantial up-front investment. The Wechsler Adult Intelligence Scale tests I went through with Camden Learning Disability Services near my 60th birthday indicate that for some intellectual functioning categories, my scores are ‘borderline’ on ‘learning disability’ range that is set at or below IQ score of 70. The subsequent report from CLDS gives me great documentation for ESA ‘Work Capability Assessment’ purposes, but no entitlement to even a formal diagnosis from CLDS that would formally diagnose my impairment/disability as dyspraxia.
Such a formal diagnosis, I am told, would cost me hundreds of pounds. So in effect, all the learning-and-co-learning hoops and hurdles I have gone through over the decades since 1978 when a Manpower Services Commission-run ‘Employment Rehabilitation Center's ‘Occupational Psychologist’ [sic] told me that my career difficulties stemmed from “a birth defect” have benefited me nothing in terms of employment credit.
Right wing ‘welfare reform’ is not really about rewarding effort and ‘saving disabled people from worthlessness’, but the privatization of the welfare state and screwing the economically vulnerable. Benefit sanctions and threat of sanctions are really a means of unconscionable global corporations finding commercial profit in exploiting the people they would previously have ‘parked’ as not worth the current time of day.













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