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Please help Karina Hansen, severe ME patient, by signing these petitions! Video link included!

Discussion in 'Petitions' started by COACH, May 31, 2013.

  1. maryb

    maryb iherb code TAK122

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    I don't think the mother has been at Karina's bedside for some months now. None of the family have been allowed to see her. Therefore one could say 'shouldn't there have been some improvement in Karina's condition if the psychiatrist and his team blame her illness on her mother?
    that is the main question the authorities should be asked.
    taniaaust1, justy, SOC and 1 other person like this.
  2. tatt

    tatt

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    COACH, justy, maryb and 1 other person like this.
  3. maryb

    maryb iherb code TAK122

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  4. justy

    justy Senior Member

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  5. justy

    justy Senior Member

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  6. COACH

    COACH

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    Please check out all the new information on Justice for Karina Hansen's facebook page and website. There is a new petition specifically to get her a second opinion. There is also a thunderclap to sign up for. On Feb12 Karina will have been held at Hammel for one year! She needs all of us to help her and her family get her the correct treatment. Here are some links to get you started. Thank you!
    1. change.org link http://chn.ge/1itYO0i
    2. thunderclap link: http://thndr.it/1nUTVRm
    Ren likes this.
  7. Little Bluestem

    Little Bluestem Senescent on the Illinois prairie, USA

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    Where is Katrina's Website?
  8. COACH

    COACH

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    justiceforkarina. webs . com With no spaces though. My mobile device is not cooperating with me. Sorry.
    Little Bluestem likes this.
  9. Little Bluestem

    Little Bluestem Senescent on the Illinois prairie, USA

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    Also interesting that the nurse just happened to go in and ask Karina if she wanted a visit before Jens Gyring was contacted again. So very convenient.
  10. taniaaust1

    taniaaust1 Senior Member

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    This kind of thing is probably going on worldwide eg Brian too.

    We can only be hearing about the tip of the iceberg here. How many are severely sick with ME and are locked away to be never heard of again? due to families not knowing they have ME or whatever. A bit a large percentage of ME people are never diagnosed with ME/CFS due to symptoms being seen as too severe (as much doctors think CFS is just about being slightly tired with a few minor symptoms and not about someone who just really cant get out of bed, has MCS (which many doctors wont believe) etc etc

    There needs to be a fund set up or something set up to help people world wide in this situation.. Im all for secret safe houses if need be to protect people from those who should be reallly helping us but arent. (I'd hide someone in my home for a while if someone needed it in this situation). Just imagine the media outcry if someone did this and hide a ME person in another country to protect them (even hiding a child from this abuse).. maybe that is what we need to happen to gain media attention of this shocking abuse which is going on.

    .........

    I personally fear the same thing could happen to me as my condtion is slowly worsening due to lack of support of state disability service who wont recognise my ME/CFS and I have been long term bedbound with it before (but fortunately back then I had a child home to care for me). If my condition keeps deterioating due to constantly having to over do daily life stuff.. what is going to happen to me? I only have CFS specialists who believe ME is CFS and who arent even aware of the symptoms of ME. If things continue for me the way they are.. something is going to end up having to happen in my case! Are they going to recognise I need support for my ME or will I get locked up?????

    I have been hospitalised before due to becoming suicidal and while I was there.. my ME was completely ignored!! I got threatened with being dragged out of bed for breakfast even thou I hadnt had enough sleep etc etc. Had I not been able to 'make out" I was fine at the time to excape the place.. I would of further deteriorated with my ME due to the mental health ward not being suitable for me. (no sound sensitive ME patient as I was at the time should be put right next to the patients recreation room where noise is coming from all day etc so one cant get the rest one needs). That place would of killed me.

    The more I think about it.. the more I think I should be taking some legal steps now to try to keep myself safe in future.. I think should be signing something giving my CFS sister legal authority to make all medical decisions etc for me should I be deemed not sound to do so.
    Last edited: Feb 13, 2014
    COACH likes this.
  11. taniaaust1

    taniaaust1 Senior Member

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    That petition site..change org or whatever its called.. never allows me to sign petitions there as it wont accept my address (and I tried to put it in different orders etc without luck).
    .............

    OMG.. I just read she was given a diagnoses of Pervasive refusal syndrome and just looked up what that supposively is http://en.wikipedia.org/wiki/Pervasive_refusal_syndrome . Looks like the psychs are having a field day with thier new diagnoses.

    • umm so what is the difference between this new psych disorder and CFS diagnoses? anything? I think we all should be concerned about this new psych diagnosis.
    So the psychs have covered the viral infection angle too and that wont rule a person out.. created a new mental health disorder which starts with an viral infection.

    Very interesting that they are now blaming those things for mental health disorders!! This is soo crazy. Where are the psychs going too stop?

    Im worried about the IOM stuff and now I see this.. very very scary.

    So in other words any severe ME person may fit all that as often those who are trying to help may be hurting the person who movement, light, sound or other things may be too much at times esp if the person trying to help dont understand at all.

    I think this diagnoses should have its own thread for discussion so Im going to give it one. Anyway wanted to mention it here seeing I saw that is what they've decided to diagnose Karina with
    COACH likes this.
  12. leela

    leela Slow But Hopeful

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    @taniaaust1 this is horrifying! very worrying.

    Why don't they just rename psychiatry "Refusal to Acknowledge Self- Awareness and Autonomy in Fellow Humans Disorder."
    taniaaust1 and Little Bluestem like this.

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