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!
New Exercise Study Brings Both Illumination and Questions
Simon McGrath looks at new objective evidence of abnormal response to exercise in ME/CFS patients, and the questions that researchers are still trying to answer ...
Discuss the article on the Forums.

WSJ's blog: The AABB Makes it Official: CFS Patients Shouldnt Give Blood

Discussion in 'Media, Interviews, Blogs, Talks, Events about XMRV' started by Lynn, Jun 19, 2010.

  1. Lynn

    Lynn Senior Member

    Messages:
    301
    Likes:
    51
  2. V99

    V99 *****

    Messages:
    1,471
    Likes:
    1
    UK
    Thanks tloyd.
  3. JT1024

    JT1024 Senior Member

    Messages:
    534
    Likes:
    288
    Massachusetts
    There were a number of comments to the WSJ blog article. One was by a physician (see below)

    1:54 pm June 19, 2010
    Susan Goodner wrote:

    Does this mean that those of us who have been diagnosed with Chronic Fatigue Syndrome and have developed some of its complications such as measurable deficiencies in immune function and low blood pressure that appears related to an immune defect and can result in fainting are being regarded as folks who have an actual disease instead of like neurotics? I loved my job as a family doctor and cared deeply about my patients. Kids I delivered are still graduating from the local high schools. I have not been able to practice for over 2 years due to this invisible disease. Please allow all those diagnosed with the dignity afforded to those disabled by a chronic illness, whether you understand it or not.


    There was another comment by a "JT" that wasn't me!

    ~ JT

See more popular forum discussions.

Share This Page