Social Care Archives - Chronic Illness Inclusion

It’s Our Community

10 March 2021 Editorialteam CFS, Chronic Illness, ELCI, Energy Impairment, Energy Limiting Chronic Illness, Housebound, ME, Social Care, Social Exclusion

Catherine Hale spoke at It’s Our Community, a conference on social care reform. Catherine explained the high prevalence of energy limiting conditions and the psychological impact of not being believed.

I was a social care user back in the 1990s. I’ve had my chronic illness for over three decades and when it was really acute, and I couldn’t wash feed myself, or go to the loo, I had a care package. But later years when things were less severe, my needs were harder to grasp because my impairment was invisible and poorly understood. The social care system completely let me down. As a disabled lone parent I had no support.

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On not being believed

27 January 2018 Editorialteam Chronic Illness, Chronic Pain, Disability, DWP, Energy Impairment, Energy Limiting Chronic Illness, Mental Health, Systemic Disbelief, Wheelchair

Wheelchair Vista on the lasting effects of being doubted.

Many of us with long term conditions struggle to accept that we can no longer live life as we used to. It took me almost ten years.

I carried on working for longer than I should. A resident at the care home I managed said; “It’s doing you no good keeping on working. Why don’t you reduce your hours or stop altogether?” She saw that I could not stand for long without leaning against a wall. Staff noticed that I always relied on the lift and was often in urgent need of the loo.

When I had time off work for minor surgery it had to be extended due to massive bruising sustained in a car crash. This was soon followed by investigations for IBS and a referral for knee surgery, which culminated in my employment contract being ended.

From ‘sick’ to ‘disabled’ – my own journey

13 June 2017 Editorialteam Brain Fog, CFS, Chronic Illness, Disability, DWP Benefits, ELCI, Energy Impairment, Energy Limiting Chronic Illness, Housebound, ME, Social Model of Disability

Catherine Hale considers how half a lifetime of chronic illness has changed her understanding of the term ‘disabled’.

I’ve been sick for nearly 30 years. That’s the whole of my adult life. I always thought of myself as ‘disabled’ in the sense of being very incapacitated. During my bedbound phase I couldn’t wash, feed myself, go to the toilet or write my own name; nor could I read, watch TV or have a conversation.

But I never thought of myself as ‘disabled’ in the political sense used by the disabled people’s movement. That is, I never thought the disadvantages I suffered in not having a job, a career, or a social life were due to an infringement of my rights. It didn’t make sense to blame my profound isolation on other people or organisations excluding me unnecessarily or treating me unfairly.