My daughter is going to be treated against her will. But that s because she is autistic (that's not the treatment issue) and has developed very severe OCD and is now well into the process of becoming anorexic. She has a poor understanding of the consequences of trying to control her environment by not eating or drinking. For this reason, treatment against her will is absolutely justified so we can find out why she's doing this and find ways to make it so she doesn't have to do it anymore.
ME/CFS, on the other hand, is not an issue for involuntary treatment orders such as the one going on here. For this reason, I'm signing.
I'm so sorry to hear about your Daughter Daibhidh. It must be heartbreaking to have to go through. Not to mention soul destroying when the people we turn to in our hour of need are the ones who are making the situation worse. I just hope they begin listening and give the right treatment. And hopefully you can turn to a support group for help. And if you started a partition I'd sign in a heart beat
Thank you KP. It is indeed that. And yes - sadly the system here in Finland is ... largely crap, and expertise is slow to seep in. And it's heartbreaking to have to face one's child who wants to go home but isn't able to cope at home. As it is, I get to see her very rarely: her mum's new hubby is a complete worthless letter, shall we say? He has a history of violent behaviour for no just cause and still he is in the house. I see him as a major factor in the aetiology of my daughter's issues. And thank you.
So Sad about your daughter, No words for what is happening to so many, all Our Love And Lightxo
Please , Please sign this petition these are crines against Humanity , Anyone of you or your loved ones can be diagnosed with ME/CFS Offering NO sollution to your illness !!!
Yes anyone can develop m.e and if they can mistreat one of us like that they can mistreat all of us
And we think we have it bad in the USA!
Another bunch of moronic so called professionals with no more knowledge of the subject than a dyslexic chicken. If I were in denmark I'd go and get her out and return and kick the shit out of the hospital staff.
13 years I've put up with this sort of generic ignorance. I'd give em a piece of my mind if I had any left.
I pray for you night and day Karina. What an awful situation you have been placed in. You are dealing with not one but two evils. This truly is abuse at the hands of professionals. Xxx
I CANT BELIEVE THEY WOULD DO SUCH A THING! IT IS TOTALLY DISGUSTING AND INHUMANE,SO VERY SORRY FOR THIS POOR GIRL.LETS PRAY NO OTHER PERSON IS BEING TREATED THIS WAY!
This must be a human rights violation - why isn't it being taken to the european courts? They would have to consider medical evidence from around the world showing that there are physical problems behind this illness. They could kill her, there is certainly no evidence her condition has improved.
Sadly, that path takes money. Most people haven't even enough to go to their own courts, especially when governments are stripping back the legal aid funding.
She and her family are being assisted, BUT, due to the fact the Doctors/Facility/Government people involve refuse to answer any questions, provide and paperwork, they might do harm to her case. They are watching things very closely and are proceeding with various legal options to try to get access to the very basic information so that they may find out WHY she was forcibly taken and under which laws she is being held without her consent.
This is not by any means the first time this has happened and will not be the last.
But if everybody keeps up the EXELENT WORK off spreading the word via misc social networks and so on. . at least in DK , allmost the last time. .
That's it Dennis we just have to keep spreading the word and keeping the pressure up. like the movie the shawshank redemption just keep sending more and more letter until they have to give in
omg exatly what an exelent example!! aparently somthing is going on here in DK 2days ago i looked to be al long battle. . but now they ( ME foundation ) have in writing from misc Doctores where they denie everything. . that she can be wisited by whom ever. . and they are apparently beginning to acuse each other. if the are so stupid as to give the ME Foundation proff in writing. . ( even police repports has mystyrily ben misplased and so on ) this wil come and bite them in there a** sooner than expected i hope. .
Im in direct contact with karinas parrents. . ( via my childhood and still best frind karina`s bigbrother. .) som im following this closely as i have seen how much this affects not just karina but her parrents witch is in a serius financely problem and have ben forced to sell house and every thing to pay medical bills. . because she vas removed from our social health security arrengment. . witch no one i ask even thougt was possible as this follows you fro your born
God I had no Idea could you at that story to our facebook page www.facebook.com/JusticeForKarinaHansen
So sad but thank you for that update, selling a house to pay for mistreatment that is killing her, no words for the extent of this disgrace...
I have the same disease.
It is an awful illness isn't it. I went from very fit to very severe and bedridden in an instant. It was like being tortured every second of the day and the idea that someone could come and force me out of my home while I was in that state is horrifying. And when I tried to exercise my way back to health I just got worse and worse. So I know from experience that these Doctors do not know what they are doing.
Chapter 33 of Hillary Johnson's: Osler's Web: Inside the Labyrinth of the Chronic Fatigue Syndrome (CFS) Epidemic is "HIV-NEGATIVE AIDS."
Neenyah Ostrom's book "America's Biggest Cover-up: 50 More Things...CFS & Its Link To AIDS" cites: "Some CFS Patients May Be Non-HIV AIDS Cases."
Will CFS ever make any progress unless we acknowledge this fact?
Published 14 times on 4 continents, my life w/ NON HIV AIDS: www.ukprogressive.co.uk/the-aids-like-disease-seldom-mentioned/article20891.html
Or simply google “NON HIV AIDS”
Cfs is not linked to aids. Please do your research properly thank you