1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
    Check out the website, Facebook and Twitter. Join in donate and spread the word!
Knitting Equals Pleasure, Despite ME/CFS
Jody Smith loves knitting. Again. She thought her days of knitting and purling were long over but ... she's back ...
Discuss the article on the Forums.

UK XMRV demo 1st November

Discussion in 'Action Alerts and Advocacy' started by Kate_UK, Oct 20, 2010.

  1. Min

    Min Senior Member

    Messages:
    1,297
    Likes:
    1,585
    UK
  2. Sasha

    Sasha Fine, thank you

    Messages:
    8,716
    Likes:
    7,983
    UK
  3. Tia

    Tia Senior Member

    Messages:
    247
    Likes:
    19
    When will Sweden put a ban on it? Why doesn't anything happen over there? Noway at least have mobile teams for ME-patients. Sweden has NOTHING, they're like a poor old country that knows nothing about ME. They don't ecen know what ME is.. A friend over there said the doctors asked him if he didn't mean MS, when he said ME, and they said it in a tone as.. - Yes, u mean MS.. Moron doctors with no training in this! When will this stop? When will the doctors there be more educated then their paitents?
     
  4. Fibrobabes

    Fibrobabes

    Messages:
    9
    Likes:
    0
    thanks everyone
    FB
     
  5. Sasha

    Sasha Fine, thank you

    Messages:
    8,716
    Likes:
    7,983
    UK
    Nice picture, Fibrobabes, very glam & retro!
     

See more popular forum discussions.

Share This Page