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M.E/C.F.S Patients' Legal Fund

Discussion in 'General ME/CFS news' started by Jan, Sep 6, 2021.

  1. Jan

    Jan Senior Member (Voting Rights)

    Messages:
    498
    ''I'm Sally Callow, Founder of ME Foggy Dog, a social enterprise based in the UK. As an advocate, I have noticed that increasingly over recent years, the M.E/C.F.S patient community has been frustrated at the perceived lack of legal action from M.E/C.F.S charities in relation to political decisions and what appear to be breaches of the law by Government and policymaking organisations.

    The aim of this fund is to enable the M.E/C.F.S patient community to take legal action in the absence of action taken by charities.

    This fund will enable future legal cases relating to matters that directly affect at least half of the UK patient population i.e. not individuals or specific areas/clinics of the UK.''


    Link to fundraiser https://www.crowdfunder.co.uk/mecfs-patients-legal-fund
     
    lunarainbows, Hutan, Ash and 8 others like this.

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