Looking Ahead to Change: Little by Little
I don't make New Year's Resolutions. I don't think I ever really did, but the last decade or two would have been enough to stifle that impulse. I've just been too aware that I don't have that much control over what happens in my life.
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Catherine Hale - "The politics of stigma with ME/CFS"

Discussion in 'General ME/CFS News' started by worldbackwards, Dec 17, 2015.

  1. worldbackwards

    worldbackwards A unique snowflake

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    Great blogpost from Catherine Hale, taking in PACE, stigma and access to care and treatment.
    http://limitedcapability.blogspot.co.uk/2015/12/the-politics-of-stigma-with-mecfs.html
     
    Last edited: Dec 17, 2015
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  2. Little Bluestem

    Little Bluestem All Good Things Must Come to an End

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    bump
     
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  3. octoberpoppy

    octoberpoppy

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  4. Aurator

    Aurator Senior Member

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    It's a brilliant and moving article that perfectly encapsulates the unique cruelty that people with ME have had to endure in a world that has been repeatedly persuaded of their unworthiness. And it puts to utter shame the people who have been responsible for doing the persuading.
     
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  5. octoberpoppy

    octoberpoppy

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    Thank you. I normally research and write in the field of welfare benefits for sick and disabled people and social care in the UK, so this is a bit of a departure for me. But my hope is to bring awareness of this injustice to the community of disability activists in the UK. I find many parallels between our story and the struggle by the disabled people's movement for the right to independent living, for example.
     
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  6. waiting

    waiting Senior Member

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    @JenB -- great post to highlight in ME Action re: stigma & strategy and PACE criticism.

    Edit: Jen, you are quoted near the end of her article, too. And a link to your website.
     
    Last edited: Dec 20, 2015
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