Norway Combats the "Stress Theory" for ME/CFS

This article by Ola Didrik Saugstad was originally published 14 July 2015, at. 8:00 in leading Norwegian newspaper Dagbladet.no. Excerpts from the online English translation below.

Undocumented treatments have led to some of the worst disasters in the history of medicine.

Many ME patients feel today that the public health system is exacerbating their condition.

Dr Ola Didrik Saugstad, professor of pediatrics as the University of Oslo asks, “Should we not learn from the mistakes made by researchers with home knitted hypotheses?”
Saugstad opens by describing two historically invalidated hypothesis that had far-reaching implications and damaging effect.
Bettelhiem “believed that the mothers of autistic children were cold, so-called «refrigerator mothers» who hated their children and thus induced autism on them. Today we know that autism is a complex biological disease. Bettelheim, who also believed allergy is psychologically triggered, did irreparable damage with his undocumented hypotheses.”
Dr Spock’s recommendation that babies sleep on their stomachs and “contributed greatly to the thousands of infants who died in the SIDS epidemic culminating in the late 1980’s when they realized that laying the babies on their stomach increases the risk of SIDS.”

Bettelheim and Spock are examples of authorities who did not base their recommendations on scientific evidence, but on their own thoughts and beliefs. We should learn from this not to make similar mistakes. But do we?
An example on how we don’t, is the stress theory that has become popular as an explanation for ME. Many believe that one can be cured of the disease by mastering ones’ own stress. «It’s all in your head, you just need to convince yourself to get well», many patients have been told. But this explanation has never been scientifically proven. On the contrary, those behind the stress theory have selectively used some findings that fit with their own hypothesis. This is what is called an inductive fallacy.
It was such a catastrophic failure Bettelheim and Spock did, and now it seems that the same mistake has been made by those who believe that ME is a stress response.

Saugstad goes on to detail some of the new research studies and reports that have come out saying that ME is truly a physiological disease, not a stress response or psychological condition:

  • “a new report from the Institute of Medicine in the US states that ME/CFS is a physical condition, not a mental illness.”
  • “Columbia University Press could report from a study that showed that ME/CFS patients sometimes have very high levels of inflammatory markers, cytokines, but only early in the disease. Later, patients often have lower levels than in healthy controls. This may explain why studies on inflammation markers in ME have given contradictory results.”
  • Another recent study has shown that muscle cells from ME patients respond differently than healthy muscle cells to electrical stimulation. ME muscles do not take up glucose as one would normally expect.

Despite the inconclusive scientific basis, the stress theory has received considerable support in the Norwegian health care system and in the public. Now we understand why many ME patients feel that the public health system is exacerbating their condition. Many feel they are being bullied by NAV [the National social welfare system], and parents are threatened by child protective services because they protect their child from the harmful stress theory. Conditions have developed so that ME-patients’ situation in Norway has become a human rights’ problem.

Facebook
Twitter
WhatsApp
Email

Latest News

a blue square image that features waves as the background. The 2025 #MillionsMissing logo at the top. followed by the words, Why We're sending out an SOS. A life preserver is in the bottom right corner and the meaction logo is in the bottom left corner.

Why We’re Sending out an SOS this #MillionsMissing

On May 12th, #MEAction and the #MillionsMissing are sending out an SOS to Congress to Save our Support Systems. Save our Science. Save Our Society.  HERE’S WHY: Healthcare, research funding and accessibility were already incredibly fragile for people with myalgic encephalomyelitis (ME), Long Covid and the disability communities. Now, we are seeing constant threats to

Read More »

Writers Guild Initiative Writing Workshops: Apply Today

#MEAction is excited to announce we are partnering with the Writers Guild Initiative (WGI) again to offer creative writing workshops for people with ME and Long COVID**. WGI has graciously donated their time to offer these writer workshops through personal mentorship with the writers of the #MEAction community! The workshops consist of three sessions during

Read More »
Purple rectangle. on the left: image of the book cover for Nobody's Empire. On the right the words: Virtual Interview + Q&A with Stuart Murdoch. MEAction logo on the bottom corner.

Virtual Interview + Q&A with Stuart Murdoch

Stuart Murdoch, from the band Belle and Sabastian, will be interviewed by #MEAction Minnesota’s State Chapter Leader, Terri L Wilder, about his recently released novel, Nobody’s Empire, on Saturday, April 19th at 1pm ET/6pm BST. We hope you join us for this virtual event to learn more about his debut novel. Tickets are available for

Read More »