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The local Danish newspaper Ukeavisen Esbjerg has written several articles about a severe ME-patient who is bed bound and nursed by her parents, and whom the municipality sees fit to work and thus not in need of welfare money. Today the newspaper print a manifest made by 85 ME-patients who tell...

That was easier said than done.. I've uploaded pictures but don't know how to add them in the correct album. Is there a step-by-step-procedure somewhere? Edit to add - or an e-mail address I can send photos to so MEAction can upload themselves?

Local TV station in Stavanger, Norway with a short section about Saturday's demonstration. TV Vest: Norges største samling på ME-dagen (Norway's biggest event on the ME-day)

(Norway) Rogalands Avis: Stor markering i Stavanger på ME-dagen Big event in Stavanger on the ME-day Article is behind paywall but had several great pictures of shoes and speakers, good information about ME and the lack of care. One of the speakers were a mother of a severe ME-patient. The...

Local newspaper in Stavanger, Norway about today's MillionsMissing event. Very nice article with lots of pictures from a large shoe installation, interviews with several people including professor Saugstad who says: May 12th is the ME Awareness day. I have participated in this for several years...

The Norwegian ME Association - Oslo and Akershus county - has made a video with interviews of Norwegian ME researchers for 12th May. I hope someone is working on subtitles in English. The film contains an interview with professor Ola Saugstad about the IOM report, increased research in USA, and...

From Stavanger, Norway A great day and a great turnout! Several journalists came. Hopefully there will be some good coverage. For now the Norwegian public broadcaster has shared a photo and short description of the demonstration. NRK: Sko for myalgisk encefalomyelitt google translation: Shoes...

Merged thread Two allocations from The Norwegian ME Association to research The Norwegian ME Association celebrates 12th of May by allocating funds for two research projects into ME. The research group for ME/CFS at the cancer ward at Haukeland university hospital (prof. Olav Mella and MD...

Those who have developed the robot, AV1, just tweeted this :)

Letter-to-the-editor by psychologist and ME-patient to the newspaper Dagsavisen Problemet med hvordan vi forklarer ME google translation: The problem of how we explain ME Focus on psychosocial factors has not reduced prevalence. ME is the main reason for sick leave at school. During the last...

Letter-to-the-editor by chairman and general secretary of the Norwegian ME Association to the newspaper Dagsavisen. Håp for ME? google translation: Hope for ME?

Sissel Sunde is behind the largest MillionsMissing event in Norway tomorrow. It all started with a guest blog post at one of the biggest bloggers in the country, where Sissel told her story together with information about ME, research and the MillionsMissing movement. The blog post was shared...

This is a wonderful, beautiful album with short songs accommodated for people with low listening capacity. The songs are made by Anette Gilje, a sufferer of ME for many years. The texts reflect several aspects of living with this disease. Anette is a great advocate for ME in Norway. She was...

Thank you for bringing context and nuances to the editorial, @mango :-)

Same post on OMFs website: OMF funded Severely ill Big Data Study

Here are their posts about the article on Facebook and Twitter, for those who want to like, share, and/or comment.

It does for a second, and then an error message appears (at least for me).

Thank you @Helen for the translation I am not sure how to make a google translation link from the editorial, but usually someone on the forum can help when I'm stuck. I'm under the impression that with a google translation link internet's wonderful ways somehow ensures that also the original...

Excellent editorial from the Swedish Aftonbladet, whom lately has had several articles on ME (see recent posts on this thread by @mango ) It is a strong support to ME-patients and to proper welfare for this patient group. For some reason I was not able to google translate this. Perhaps others...