ever since the Dagbladet articles about the "ME-war" 16. may and pinsehelga I have tried to sit on your hands. I thought to let it blow over. I would not throw me into a debate where the fronts are so steep that politicians refuse to engage, and the media are reluctant to write.
But the sick feeling is in. Consequences such as further stigmatization has for ME-ill children and adults release me. Nor does it unreasonable that the health care professional represent themselves as the victims in connection with a disease where its client scores lowest on quality of life and physical function, in which one of the four is house - and sengebundne, more sondenærte and the risk of suicide is high.
the Newspaper quoted a letter written by a patient to a health care provider, referred to a blogger, and referred to the messages from closed forums where WE-ill patients share the grief of serious illness, and conveys the frustration of an apparatus as a claim that the therapy and exercise do healthy.
Or as a trygderettdommer said earlier in the year, that WE-sick can be good to take steps as, for example, to "switch partner".
Harassment is never ok, regardless of whether it comes from the depressed who have to wait too long for help, the cancer patients who got the diagnosis too late, MS - sufferers who think they are feilbehandlet or ME ill as to object to treatment that does not work.
But we as health professionals must be able to withstand that patients may be angry, afraid or disappointed. We must accent that they do not experience themselves heard, not experience their sykdomserfaring validated or that they are not receiving adequate reliever.Turn On the LydErrorAllerede plus customer? Log into herError STALL FRONTS: A number of professionals, among them research director Signe Flottorp in FHI, believes a warning sent out from NAFKAM, a group of experts funded by the public, is an example of the steep fronts in the ME debate. Video : Nina ... Show more
Our job is to listen to feedback from patients. And when many patients conveys that action makes them lasting worse, we have to listen extra well.
Doctors and psychologists have a large influence on a treatment procedures. Patients are depending on our expertise and committed to our assessments. Maktforholdet is biased – to the health advantage.
When ME patients who want differentiated and up to date treatment be described as the destructive activists, this affects the trust and cooperative climate. The term voices not. Studies show that WE-the sick are not more aggressive than other sick.
My hope is that future coverage of ME emphasizes the fact that the WHO classifies the illness as neurological. That the exercise-induced deterioration is a prerequisite for ME-diagnosis, and that the NIH has removed cognitive therapy and degrees of training from behandlingsråd.
I wish a constructive focus aimed at promising breakthrough in the research and towards the health professionals who use their expertise in collaboration with the patient to create the best possible living environment in anticipation of the effective treatment. As well as some tales tell about brave children and young people who endure an inhuman lidelsestrykk and a strong bereavement for the life they want to live.Full-ME war: - Never experienced similar You can submit your article and opinion piece in Dagbladet here
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