Jilly Washington
Jilly Washington

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 !!!

Kojak Peg
Kojak Peg
  • Jilly Washington

Yes anyone can develop m.e and if they can mistreat one of us like that they can mistreat all of us

Shirley Hobson Chapman
Shirley Hobson Chapman

disgusting behaviour by people we should be able to trust

Kojak Peg
Kojak Peg
  • Shirley Hobson Chapman

Yes these are people we turn to in our hour of need and all they can do is ridicule and mistreat you. And the most disgusting thing is they have law on their side

David Doherty
David Doherty

A disgrace...all our love and light to Karina and her family, the world is watching 'Hammel Neurocenter' VERY closely...

Kojak Peg
Kojak Peg
  • David Doherty

It should be called HMP (Her Majesty's Prison) Hammel Neurocenter

David Doherty
David Doherty
  • David Doherty

So true... and so so sad:(

Karen Turcotte
Karen Turcotte
  • David Doherty

Help This Young Lady , She Has The Right To Be At Home With Family !!!!!!!!!!!!

Elsie Anne Owings
Elsie Anne Owings

Oh, no!!! This is every ME sufferer's worst nightmare. I suffer from ME, but I have been a bit more fortunate: my doctors in the USA have taken my illness seriously even when they couldn't offer much in the way of treatment. And I have (finally) laboratory tests showing that some of my immune cells aren't functioning, and some types of viruses that should be dead or dormant in my system are instead flourishing.
If Karina had been offered this type of testing, she, too, would show...

Oh, no!!! This is every ME sufferer's worst nightmare. I suffer from ME, but I have been a bit more fortunate: my doctors in the USA have taken my illness seriously even when they couldn't offer much in the way of treatment. And I have (finally) laboratory tests showing that some of my immune cells aren't functioning, and some types of viruses that should be dead or dormant in my system are instead flourishing.
If Karina had been offered this type of testing, she, too, would show abnormalities. But doctors who don't want to take the disease seriously don't offer anything except the old standard tests that won't show anything.
Not only are this young woman's civil rights being violated, this appalling act of medical malpractice is endangering her life.

Elsie Anne Owings
Elsie Anne Owings
  • Elsie Anne Owings

Unfortunately, complaints from the patient community will be viewed as insignificant, since this type of medical professionals consider us to be nothing more than chronic complainers anyway. These "doctors" need to hear from other doctors; the ones who actually specialize in ME research. And no, that doesn't mean the ones from Kings College in London. They should contact the IACFS/ME and chat with some of the professionals who have been truly researching this disease, not those who have been making money by trivializing it.

Kojak Peg
Kojak Peg
  • Elsie Anne Owings

Very true Elsie, but hopefully it will add weight to the arguments already being put forward to the Danish Government. And if it make one minister think twice about it. Then it's been a success

James Dickson
James Dickson

I also had chronic ME and I left me severely disabled and bed bound for just over 10 years. I was not treated with understanding by British doctors, their ignorance was disgusting. I was left at home suffering in pain and sever disability and they did not care or try and help. At the time the NHS did not train their doctors to understand or treat the illness. I was only given help 8 years ago when dr obrien at Southend hospital discovered my plight and approached the primary care trust for...

I also had chronic ME and I left me severely disabled and bed bound for just over 10 years. I was not treated with understanding by British doctors, their ignorance was disgusting. I was left at home suffering in pain and sever disability and they did not care or try and help. At the time the NHS did not train their doctors to understand or treat the illness. I was only given help 8 years ago when dr obrien at Southend hospital discovered my plight and approached the primary care trust for funding to send me to the chronic fatigue syndrome unit at old church hospital under professor Finley. I was great full of the opportunity to get my life back and worked hard. I left hospital a year later well enough to live on my own. Another year later I had made a full recovery. I am living proof that even the most severely effected ME sufferers can be treated successfully and make a full recovery. All it takes is doctors to recognise the serious nature of the illness and try and help.

Kojak Peg
Kojak Peg
  • James Dickson

And the most worrying thing is the UK is on of the most informed countries about m.e

Sarah Balfour
Sarah Balfour
  • James Dickson

I've been sectioned several times too. I've been becoming more and more sick for the past 2-3 years. I'm in constant pain, constantly fatigued lethargic and hungry - and a few days ago, I noticed my spine was curved!

Sarah Balfour
Sarah Balfour
  • James Dickson

Whoops! Don't know what happened there!

Willõ Withywindle
Willõ Withywindle

This is not by any means the first time this has happened and will not be the last.

Dennis Østergaard
Dennis Østergaard
  • Willõ Withywindle

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. .

Kojak Peg
Kojak Peg
  • Willõ Withywindle

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

Dennis Østergaard
Dennis Østergaard
  • Willõ Withywindle

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. .

Dennis Østergaard
Dennis Østergaard
  • Willõ Withywindle

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

Kojak Peg
Kojak Peg
  • Willõ Withywindle

God I had no Idea could you at that story to our facebook page www.facebook.com/JusticeForKarinaHansen

David Doherty
David Doherty
  • Willõ Withywindle

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...

Blair Stanovie
Blair Stanovie

this is terrible, let the girl go or the parents should bring charges against the doctors and the people hollding her. If they don't beleive her, let her go

CJ Janzen
CJ Janzen
  • Blair Stanovie

They have to find out what laws the doctors are using first before legal action can be taken. We should be receiving an update on her status this coming week.

Ambrosine Yolanda Shitrit

I have had ME chronic fatigue syndrome for nearly 25 yrs. The first year or so i was bed bound. My mother and father had to care for me day in day out. I lost my career at the time, and was so fatigued I could not think.
I had virtually the same symptoms as this girl, and I was housebound for a while. Slowly i changed my diet to a purely vegan, and slowly at home started to exercise and move around. It took nearly 2yrs till I started to feel better etc.
Managing M.E at home, is the best and...

I have had ME chronic fatigue syndrome for nearly 25 yrs. The first year or so i was bed bound. My mother and father had to care for me day in day out. I lost my career at the time, and was so fatigued I could not think.
I had virtually the same symptoms as this girl, and I was housebound for a while. Slowly i changed my diet to a purely vegan, and slowly at home started to exercise and move around. It took nearly 2yrs till I started to feel better etc.
Managing M.E at home, is the best and only thing to do, as hospitals and doctors still have no idea of how to manage it.
Eat well, naps, sleeps and plenty of love is the only way to start to improve.
I never got better , but I learnt to live with it.

Helen Charles
Helen Charles

This is really bad...surely they can realise this girl is physically sick...have they tried tests and things or are they so blind that they are set in there ways

Kay Karen Lambert
Kay Karen Lambert

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”

Ian Parker
Ian Parker
  • Kay Karen Lambert

Cfs is not linked to aids. Please do your research properly thank you

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