Despite Our Losses, People with ME/CFS Want More
We've been cheated by ME/CFS and we all know it. That's a no-brainer, if you'll pardon the cognitive pun. And loss didn't just result from the bad things that befell us. It also encompasses the good things that just ... never came. The absence of bounty. Of wholeness. Of peace.
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Myalgic Encephalomyelitis: need more funding for research, awareness, support.

Discussion in 'Petitions' started by Jo Best, Dec 21, 2017.

  1. Jo Best

    Jo Best Senior Member

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    On UK Government and Parliament petition website so only UK residents or British citizens living abroad may sign: https://petition.parliament.uk/petitions/203140

    At 10,000 signatures, government will respond to this petition in writing.

    At 100,000 signatures, this petition will be considered for debate in Parliament.

    • Created by Sharon Anne Tiday (mother of young ME sufferer Shannon Tiday)
    • Deadline 20 April 2018

     
  2. Jo Best

    Jo Best Senior Member

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