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
My heartfelt prayers of healing light & much love to Karina & her family. And may the Doctors & Danish authorities find it in their hearts to honor Karina's humanness & soul.
I really do feel for Karina, as I also had CFS (recovered now) and only know too well the devasting affects ignorance can have upon a soul.
Thinking of you all - and I shall do what I can to spread the awareness & word about Karina.
With all my love,
How did you recover?
Disgusting! Poor young girl, as if her life hasn't been destroyed enough!
It is terrible and has been going on for over a year now, because they began threatening her over a year ago. And severe m.e on its own is like being tortured. So what they are doing is awful
OUTRAGED on her behalf. Surely one of the Danish Doctors has seen a paper on ME by a fellow Doctor who has had the condition first hand. Incrediblly tragic that this is happening in 2013!! This is not the dark ages! She is not mentally incapable, the GP's seem devoid of any 'understanding' so why have they decided to ACT? Is she harming anyone, bieng cared for at home? I have ME and I work p/t looking after a lady who has had the condition for some 17 years now. To her parents 'FIGHT', 'FIGHT', 'FIGHT'. X
It is outrages. I often jokingly say, I would been better off in the dark ages, but when you read about Karina you realise it isn't a joke. It is deadly serious. At the beginning of my illness I was very fit, and tried to exercise my way back to health, but it made me worse. In the end I was bedridden. Thankfully, my GPs where simply ineffectual, which although not good to begin with. Did mean in the long run, I was left to learn and treat myself. Now I can get out of the house for short...
It is outrages. I often jokingly say, I would been better off in the dark ages, but when you read about Karina you realise it isn't a joke. It is deadly serious. At the beginning of my illness I was very fit, and tried to exercise my way back to health, but it made me worse. In the end I was bedridden. Thankfully, my GPs where simply ineffectual, which although not good to begin with. Did mean in the long run, I was left to learn and treat myself. Now I can get out of the house for short walks most days, because I learned to rested. And I really mean learned.
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
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.
This all sounds very odd. Why was she removed from her home? Why no visitors? And, why can't she leave if she wants to
In Denmark, M.E. is classed as a psychosomatic illness. They removed her from her home. It's not the first time this has happened :-(
In the U.K., Sophia Mirza was sectioned, places in a mental institution and not given the proper medical care that she needed. Although she did get out, she died later :-(
Chronic Fatigue is not a mental illness.
our family's story shows they often get it terribly wrong and I am hoping by sharing it we can advocate for better treatment of Karina and every ME/CFS patient worldwide. www.bringingryanhome.com
When will this barbaric treatment stop!! I've been a sufferer fir 30 years and let me tell you people DO NOT want to be this ill. Their is no secondary gain what so ever. Please lok at the 5,000 biomedical research articles showing MAJOR problems in the brain and in autoimmunity.
The World Health Organization has recognized ME as a distinct debilitating neurological disease for decades. I know a test for it has not yet been developed but remember that MS was treated as "hysterical paralysis" before tests were developed for it.
My Aunt suffered through that misdiagnoses for her MS. She woke up blind one morning and her doctors diagnosed her with "hysterical blindness" and told her husband to put things in her path so that she would fall when walking around their...
My Aunt suffered through that misdiagnoses for her MS. She woke up blind one morning and her doctors diagnosed her with "hysterical blindness" and told her husband to put things in her path so that she would fall when walking around their home. They told him she would get tired of falling and decide to see again.
She was finally properly diagnosed 15 years later, after her husband had left her for "refusing to see". She died 2 years later from complications to the disease.
I myself suffer from either ME or a similar illness and have for the last 2 years. I have yet to get a diagnoses and have had doctors laugh at me and belittle me instead of helping. That so called professionals can act in this matter is appalling.
I'm so sorry to hear about your Aunt. It is so shocking that these misdiagnose still go on, simply because Doctors are to arrogant to admit their own limitation. And since becoming ill myself and seeing it first hand and hearing stories about it. Not only from m.e but a whole spectrum of illnesses. I've been shocked into the realisation that the people we unthinkingly put all our trust in do not always deserve our trust. And as you point out it isn't just an m.e problem it is much more wide spread than that
At midnight EST we had only 115 signatures at 6:15pm we have around 540! Please keep passing this around. We CAN and WILL make a difference!
We have spoken to Rebecca Hansen - not related - and she says they will have an update for us this coming week.