limitedcapability.blogspot.com

Limited Capability

Life, benefits and work with an invisible illness. Saturday, 8 August 2015. Severe M.E. Day 2015. In 1993 I was effectively paralysed due to severe M.E. and I lost the ability to speak, feed myself, sit up or write my own name. When my parents, in desperation, brought me to A&E because I was having difficulty swallowing the treatment offered to us was to put me on a psychiatric ward and withhold food from me until I got so hungry I would quit my histrionics and feed myself. Please look up #severeME today...

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Limited Capability | limitedcapability.blogspot.com Reviews

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Life, benefits and work with an invisible illness. Saturday, 8 August 2015. Severe M.E. Day 2015. In 1993 I was effectively paralysed due to severe M.E. and I lost the ability to speak, feed myself, sit up or write my own name. When my parents, in desperation, brought me to A&E because I was having difficulty swallowing the treatment offered to us was to put me on a psychiatric ward and withhold food from me until I got so hungry I would quit my histrionics and feed myself. Please look up #severeME today...

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6 catherine hale

7 4 comments

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Limited Capability | limitedcapability.blogspot.com Reviews

https://limitedcapability.blogspot.com

Life, benefits and work with an invisible illness. Saturday, 8 August 2015. Severe M.E. Day 2015. In 1993 I was effectively paralysed due to severe M.E. and I lost the ability to speak, feed myself, sit up or write my own name. When my parents, in desperation, brought me to A&E because I was having difficulty swallowing the treatment offered to us was to put me on a psychiatric ward and withhold food from me until I got so hungry I would quit my histrionics and feed myself. Please look up #severeME today...

INTERNAL PAGES

limitedcapability.blogspot.com

1

Limited Capability: Other Publications

http://www.limitedcapability.blogspot.com/p/other-publications.html

Life, benefits and work with an invisible illness. Co-author: A Deeply Dehumanising Experience: ME/CFS journeys through the PIP claim process in Scotland. Action for M.E. March 2016. Close to Collapse: an interim report on access to social care and advocacy for people with ME/CFS. Action for M.E. November 2015. ESA and the fate of the Work-Related Activity Group. Published by Mind. June 2014. Submission to Fifth Independent Review of the Work Capability Assessment August. Subscribe to: Posts (Atom).

2

Limited Capability: Destitution awaits those "Fit to work" but too sick to sign on

http://www.limitedcapability.blogspot.com/2012/10/destitution-awaits-those-fit-to-work.html

Life, benefits and work with an invisible illness. Wednesday, 24 October 2012. Destitution awaits those "Fit to work" but too sick to sign on. Proposals to reform the appeals process risk destitution for sick and disabled people. A letter from my local ME support group to our MPs on another gaping hole in the safety net:. Re: government proposals on the mandatory reconsideration before appeal provision, Welfare Reform Act 2012. Several of our members who have had a “fit to work” decision over...As is wel...

3

Limited Capability: Why does stigma still surround ME?

http://www.limitedcapability.blogspot.com/2014/05/why-does-stigma-still-surround-me.html

Life, benefits and work with an invisible illness. Tuesday, 13 May 2014. Why does stigma still surround ME? Because doctors believe it's all about deconditioning. Almost nobody, except a tabloid headline-writer, says ME is “all in the mind” these days. So why is there still such a stigma attached to ME/Chronic Fatigue Syndrome? In my experience, the stigma gets. The Deconditioning Theory of ME/CFS. The deconditioning theory may be plausible for someone who presents to their GP with mild ME, e.g. ...To ch...

4

Limited Capability: Severe M.E. Day 2015

http://www.limitedcapability.blogspot.com/2015/08/severe-me-day-2015.html

Life, benefits and work with an invisible illness. Saturday, 8 August 2015. Severe M.E. Day 2015. In 1993 I was effectively paralysed due to severe M.E. and I lost the ability to speak, feed myself, sit up or write my own name. When my parents, in desperation, brought me to A&E because I was having difficulty swallowing the treatment offered to us was to put me on a psychiatric ward and withhold food from me until I got so hungry I would quit my histrionics and feed myself. Please look up #severeME today...

5

Limited Capability: Mapping Disability - Sickness and the social model II

http://www.limitedcapability.blogspot.com/2015/03/sickness-and-social-model-ii-mapping.html

Life, benefits and work with an invisible illness. Monday, 23 March 2015. Mapping Disability - Sickness and the social model II. In my introduction to this series. A Map of Disability. 8216;Ill’ is where bodily distress (pain, breathlessness, fatigue, nausea) arising from a long term medical condition results in a significant loss of global function, often both physical and mental. This loss of function is usually not fixed but cumulative in response to exertion. The more Ill someone is, th...The Ill to ...

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limitedcapability.blogspot.com

Limited Capability

Life, benefits and work with an invisible illness. Saturday, 8 August 2015. Severe M.E. Day 2015. In 1993 I was effectively paralysed due to severe M.E. and I lost the ability to speak, feed myself, sit up or write my own name. When my parents, in desperation, brought me to A&E because I was having difficulty swallowing the treatment offered to us was to put me on a psychiatric ward and withhold food from me until I got so hungry I would quit my histrionics and feed myself. Please look up #severeME today...

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