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  1. Sunshine3
    Post

    New York State: Department of Health info page

    Don't draw MS on us....leave him be!
    Post by: Sunshine3, Apr 18, 2018 in forum: General ME/CFS news
  2. Sunshine3
    Post

    A Novel Nutriceutical Treatment of ME/CFS, 2017, Comhaire

    So true, it punishes you for trying to live a little.
    Post by: Sunshine3, Apr 18, 2018 in forum: ME/CFS research
  3. Sunshine3
    Post

    Ongoing ME/CFS treatment research

    Why shoot things down so quickly??? I for one am grateful that some treatments are being trialled for us. Even if this only gives a small...
    Post by: Sunshine3, Apr 17, 2018 in forum: ME/CFS research
  4. Sunshine3
    Post

    A Novel Nutriceutical Treatment of ME/CFS, 2017, Comhaire

    @ME/CFS when approx will this treatment become available? I would be so glad of any improvement. Fatigue is a big issue for me as I need to sleep...
    Post by: Sunshine3, Apr 17, 2018 in forum: ME/CFS research
  5. Sunshine3
    Post

    David Tuller's new crowdfunding campaign (April 1, 2018)

    @Dave 30th a while to go yet, I think it will come good. My husband is called David and a complete saint. But next to him, you have got to be the...
    Post by: Sunshine3, Apr 16, 2018 in forum: General ME/CFS news
  6. Sunshine3
    Post

    Healthwise to "retire the GET/CBT topics" from medical content

    Every dog has his day is right!! Brilliant @Webdog and thank you!! It's so great to read positive news. Keep up the good work, sounds like you...
    Post by: Sunshine3, Apr 16, 2018 in forum: Advocacy Projects and Campaigns
  7. Sunshine3
    Post

    Any researchers looking at the brain?

    I'd like to see more studies on the brain...there are so few!! Afterall it's a neurological disease?
    Post by: Sunshine3, Apr 13, 2018 in forum: ME/CFS research
  8. Sunshine3
    Post

    Any researchers looking at the brain?

    I donated ages ago but the amount raised hasn't increased since....which is odd
    Post by: Sunshine3, Apr 12, 2018 in forum: ME/CFS research
  9. Sunshine3
    Thread

    Any researchers looking at the brain?

    Are there any studies underway at present looking at the brain? I know Maureen Hanson is doing brain MRIs after exercise and the intramural study...
    Thread by: Sunshine3, Apr 12, 2018, 7 replies, in forum: ME/CFS research
  10. Sunshine3
    Post

    Leonard Jason wants ME/CFS patients to do a PEM survey

    Someone who suffers from social interaction!! Isn't it an awful aspect of this illness..
    Post by: Sunshine3, Apr 11, 2018 in forum: ME/CFS research
  11. Sunshine3
    Post

    Gupta amygdala training program for ME/CFS, FM and Long Covid - news and discussion

    Totally with you Mattie, I purchased the Gupta programme too in early months of illness, what a load of codswallop. I also had sessions with the...
    Post by: Sunshine3, Apr 11, 2018 in forum: Psychosomatic theories and treatments discussions
  12. Sunshine3
    Post

    Leonard Jason wants ME/CFS patients to do a PEM survey

    Done, it wasn't too bad and covered alot. I noticed no mention of crashes brought on from social interaction such as visitors or chatting too long...
    Post by: Sunshine3, Apr 11, 2018 in forum: ME/CFS research
  13. Sunshine3
    Post

    13th Invest in ME Research International ME Conference - 1st June 2018

    Does anyone know if a dvd will be available this year of conference....I emailed weeks ago enquiring but heard nothing back
    Post by: Sunshine3, Apr 10, 2018 in forum: General ME/CFS news
  14. Sunshine3
    Post

    Very little happening!!

    I know, I Feel Like I'm always complaining, its just my health is declining so rapidly since February, I feel like I'm dying. Honestly, it's not...
    Post by: Sunshine3, Apr 9, 2018 in forum: ME/CFS research
  15. Sunshine3
    Post

    Very little happening!!

    It is Mattie and even harder when you are wasting away yourself.
    Post by: Sunshine3, Apr 9, 2018 in forum: ME/CFS research
  16. Sunshine3
    Thread

    Very little happening!!

    Is it me or is there very little happening in research news so far this year?? There are publications but nothing of significance. This time last...
    Thread by: Sunshine3, Apr 9, 2018, 14 replies, in forum: ME/CFS research
  17. Sunshine3
    Post

    Norway: ME Forening (ME Association)

    So sorry @chicaguapa, that is so awful that they would not even attend Unrest. Little by little we will chip away at the stigma hugs xxx
    Post by: Sunshine3, Apr 7, 2018 in forum: News from organisations
  18. Sunshine3
    Post

    What is Action for ME's current (March 2018) position on the PACE trial?

    That is so damaging.....it totally undermines the seriousness of ME...and if the message being put out is you can recover and get back to normal...
    Post by: Sunshine3, Apr 7, 2018 in forum: General ME/CFS news
  19. Sunshine3
    Post

    Trial By Error: A Terrific Piece about ME/CFS on Australian TV | 4 April 2018 | David Tuller

    So moving, brilliant!
    Post by: Sunshine3, Apr 5, 2018 in forum: General ME/CFS news
  20. Sunshine3
    Post

    Forward ME Group – Bodily Stress Syndrome

    Does anyone know if ME Action etc.... are stepping in and doing something...are there any ME organisations acting up to try to stop this. If this...
    Post by: Sunshine3, Apr 5, 2018 in forum: General ME/CFS news
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