Anti-Defamation Campaign in Defence of Disability Rights
Using the Law to Fight Cuts to Disabled People’s Services A practical guide for campaigners – disabled people and their families; carers and local groups (Updated July 2012)
Excellent article just thought I would point to some research from Australia from over a decade ago which pointed out:
Individuals continue to be measured as to their functional capability, or incapacity for work; the capacity of social system to support disabled people in the work place is largely ignored.
who in his right mind will employ a disabled worker if he can get ablebodied one not many so as for work other than remploy we dont get a job ,so whislt they sprout about us being employed there are no jobs for us and how the hell can we make any .without our dla and esa we woul be no roof over our heads and no food but htis lot are taking it away from us daily and its the knackers yard for most jeff3
cuts to my disibilty benefit as I have a small pension I wont get any help from the state ,but have been told “I can start my own busness”!!! doing what?!!!
I was about to have my care plan cut by 80%, which would have left me in a vulnerable position.
I read the article, and noted some of the legal points and mentioned this to the social worker. I basically said that the cuts would remove my dignity and would be detrimental to my health, which went against all of the disability laws since the 1970’s. I also said that the LA promoted ‘personalisation’, but the care package on offer was totally prescriptive with only 2 things allowed each day. She said she would talk to her manager and get back to me.
Low and behold, the following week, suddenly I was told that I’d only be losing about a quarter of my care package, and whereas I was told that no personalisation was allowed, the carers could carry on as normal (barring a few ridiculous things which I’m going to challenge).
I wouldn’t have known how to go about this had I not read this article. As a result, I can’t thank you enough.
This website uses cookies to improve your experience. We'll assume you're ok with this, but you can opt-out if you wish.AcceptRead More
Privacy & Cookies Policy
Privacy Overview
This website uses cookies to improve your experience while you navigate through the website. Out of these, the cookies that are categorized as necessary are stored on your browser as they are essential for the working of basic functionalities of the website. We also use third-party cookies that help us analyze and understand how you use this website. These cookies will be stored in your browser only with your consent. You also have the option to opt-out of these cookies. But opting out of some of these cookies may affect your browsing experience.
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.
Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. It is mandatory to procure user consent prior to running these cookies on your website.
Excellent article just thought I would point to some research from Australia from over a decade ago which pointed out:
Individuals continue to be measured as to their functional capability, or incapacity for work; the capacity of social system to support disabled people in the work place is largely ignored.
http://unsw.academia.edu/HelenMeekosha/Papers/1132887/Disability_Policies_and_Programs_in_Australia
who in his right mind will employ a disabled worker if he can get ablebodied one not many so as for work other than remploy we dont get a job ,so whislt they sprout about us being employed there are no jobs for us and how the hell can we make any .without our dla and esa we woul be no roof over our heads and no food but htis lot are taking it away from us daily and its the knackers yard for most jeff3
Equality from the top down is not Equality from the bottom up
cuts to my disibilty benefit as I have a small pension I wont get any help from the state ,but have been told “I can start my own busness”!!! doing what?!!!
great article and good comments
Thanks very much for this.
I was about to have my care plan cut by 80%, which would have left me in a vulnerable position.
I read the article, and noted some of the legal points and mentioned this to the social worker. I basically said that the cuts would remove my dignity and would be detrimental to my health, which went against all of the disability laws since the 1970’s. I also said that the LA promoted ‘personalisation’, but the care package on offer was totally prescriptive with only 2 things allowed each day. She said she would talk to her manager and get back to me.
Low and behold, the following week, suddenly I was told that I’d only be losing about a quarter of my care package, and whereas I was told that no personalisation was allowed, the carers could carry on as normal (barring a few ridiculous things which I’m going to challenge).
I wouldn’t have known how to go about this had I not read this article. As a result, I can’t thank you enough.