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We’ve all seen them in the news stories about ME/CFS: the guy in a suit at the office, yawning; the beautiful woman sitting at her desk with her immaculate make-up and elegantly coiffed hair, hand to her head and looking slightly pained.
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List of Lyme patient societies around the world (and contact information)

Discussion in 'Lyme Disease and Co-Infections' started by Aspie Lymie, Oct 26, 2017.

  1. Aspie Lymie

    Aspie Lymie

    Dear all,

    I'm a member of a Lyme patient society, and we are drawing up a list of Lyme patient societies around the world along with contact information. The idea is sharing ideas to organize events and defend our common cause on a global scale, not just locally. Additionally, we want to know what events other societies organize, and we want to share with them what we do.

    Regular researches are difficult because one has to search terms in different languages (e.g. "Borreliose Gesellschaft" to lookup German societies). It's a lot of work, and I'd like to know if you could tell me which Lyme patient societies you know already, plus if you have their contact info at hand, that would save me precious time. I know many of you here come from many different countries so I'm sure you can play your part :rolleyes: :)

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