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  1. butter.
    Post

    USA: National Institutes of Health (NIH) intramural ME/CFS study

    It is an extremely sad circumstance that this community screams for change so much and at the same time there are not enough me/cfs patients in...
    Post by: butter., Jul 11, 2020 in forum: ME/CFS research news
  2. butter.
    Post

    Juvenile myasthenia gravis unmasked: a case of a teenage female (with CFS diagnosis) who presented in acute respiratory failure, 2020, Leyens

    Reaction to the antibiotic?
    Post by: butter., Jun 24, 2020 in forum: ME/CFS research
  3. butter.
    Post

    Prevalence and Treatment of Chronic Fatigue Syndrome/ME and Co-morbid Severe Health Anxiety, 2019, Daniels et al

    You can have a severe nerological disorder and severe health anxiety, what would be surprising about that?
    Post by: butter., Jun 20, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  4. butter.
    Post

    USA: National Institutes of Health (NIH) intramural ME/CFS study

    What is the status here? Does anyone know?
    Post by: butter., Jun 19, 2020 in forum: ME/CFS research news
  5. butter.
    Post

    Peripheral endothelial dysfunction in myalgic encephalomyelitis/chronic fatigue syndrome, 2020, Scherbakov et al

    well they are just f**** for different reasons in different people, there is very unlikely one reason for all patients, what we need is trials...
    Post by: butter., Jun 10, 2020 in forum: ME/CFS research
  6. butter.
    Post

    Peripheral endothelial dysfunction in myalgic encephalomyelitis/chronic fatigue syndrome, 2020, Scherbakov et al

    of course there is, I do not understand why it takes them so long, Oaklander talks for 3 years now that SF are important for blood circulation of...
    Post by: butter., Jun 10, 2020 in forum: ME/CFS research
  7. butter.
    Post

    Short summary of meds i tried by now

    nmda antagonists,...
    Post by: butter., Jun 9, 2020 in forum: Other treatments
  8. butter.
    Post

    If there is a factor in the serum, why is plasma exchange not working?

    Personally I tend to believe that we would have found the cause of it already if it could be found with current science/knowledge/technology. I...
    Post by: butter., Jun 5, 2020 in forum: ME/CFS research
  9. butter.
    Post

    Perturbation of effector and regulatory T cell subsets in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) (2019) Karhan, Unutmaz et al

    same here! any differences in severity?
    Post by: butter., Jun 5, 2020 in forum: ME/CFS research
  10. butter.
    Post

    Perturbation of effector and regulatory T cell subsets in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) (2019) Karhan, Unutmaz et al

    So if a patient would have chronically low cd8 count (for years), what would you think about that?
    Post by: butter., Jun 5, 2020 in forum: ME/CFS research
  11. butter.
    Post

    Perturbation of effector and regulatory T cell subsets in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) (2019) Karhan, Unutmaz et al

    Is low cd8, cd8 lymphopenia a frequent finding in me/cfs?
    Post by: butter., Jun 5, 2020 in forum: ME/CFS research
  12. butter.
    Post

    If there is a factor in the serum, why is plasma exchange not working?

    Why is it so complicated to identify this? Could you give me some kind of insight into that?
    Post by: butter., Jun 4, 2020 in forum: ME/CFS research
  13. butter.
    Post

    If there is a factor in the serum, why is plasma exchange not working?

    So why isn‘t the whole world not looking for it? I mean there is a huge financial benefit to find this out!
    Post by: butter., Jun 4, 2020 in forum: ME/CFS research
  14. butter.
    Post

    If there is a factor in the serum, why is plasma exchange not working?

    So it changed something for good potentially?
    Post by: butter., Jun 4, 2020 in forum: ME/CFS research
  15. butter.
    Post

    If there is a factor in the serum, why is plasma exchange not working?

    To hear this from you sir, is very good news for me! So what factor would theoretically be responsible? Virus rna?
    Post by: butter., Jun 4, 2020 in forum: ME/CFS research
  16. butter.
    Post

    OMF to launch clinical trials on Mestinon & Kynurenine, post-COVID19 study

    there is no trap...
    Post by: butter., Jun 4, 2020 in forum: ME/CFS research news
  17. butter.
    Thread

    If there is a factor in the serum, why is plasma exchange not working?

    Any ideas?
    Thread by: butter., Jun 4, 2020, 23 replies, in forum: ME/CFS research
  18. butter.
    Post

    Plasma exchange

    hey, what dose of rapamune did you try? did it help at all? how severe are you?
    Post by: butter., Jun 2, 2020 in forum: Drug and supplement treatments
  19. butter.
    Post

    France: Bio-Modelling Systems to start phase II clinical trial(s)

    if something sounds to good to be true it is to good to be true ... when will this trial start?
    Post by: butter., May 30, 2020 in forum: ME/CFS research news
  20. butter.
    Post

    Why does levamisole help me? Mitochrondia, a7nAchR, Tryptophan

    sorry to hear that - despite or because of levamisole you think?
    Post by: butter., May 30, 2020 in forum: Drug and supplement treatments
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