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!
Nitric oxide and its possible implication in ME/CFS (Part 1 of 2)
Andrew Gladman explores the current and historic hypotheses relating to nitric oxide problems in ME/CFS. Part 1 of a 2-part series puts nitric oxide under the microscope and explores what it is, what it does and why it is so frequently discussed in the world of ME/CFS. Part 1 focuses...
Discuss the article on the Forums.

What do you all make of my illness? Esperanza here :)

Discussion in 'General Symptoms' started by Bunchy, Jan 15, 2012.

  1. Marlène

    Marlène Senior Member

    Messages:
    441
    Likes:
    214
    Edegem, Belgium
    @ judi

    who is your question addressed to?
     
  2. peggy-sue

    peggy-sue

    Messages:
    2,494
    Likes:
    2,876
    Scotland
    Bunchy's in the uk - tests of any sort are discouraged here.
    I know I've got left ventricular diastolic heart problems - my gp won't allow me to have any tests on them at all.
    I can't get tested for hormones, VO2..
    I haven't been tested for Lyme, for Parvovirus or HHV6.

    I did get allowed a haemaglobin measurement - my gp told me this is exactly the same as a haematocrit. This is a lie.
    I've performed both tests in labs - the results give totally different meanings and they're tests for completely different things.
     

See more popular forum discussions.

Share This Page