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The Times has an article today. One needs to register to read the whole article. ME sufferer who was dismissed as hysterical vindicated in death

Sciencealert has picked it up: Here's What Science Knows So Far on The Causes of Chronic Fatigue Syndrome ETA: They have over 9 million followers on Facebook ..and 68 K followers on Twitter

Yes, you are right, @andypants That was an excellent article. I completely forgot to post it here! ME-patient Ragnhild recently turned 30 years old. She wished for donations to OMF as birthday presents and raised over 35 000 NOK (4 300 USD, 3200 GBP). She explains life with ME very well. Linda...

Absolutely, and I wonder if part of the explanation is that the documentary maker spent two years making the film and that some of the journalists at TV2 have some knowledge about ME from before. That is why it is so crucial to get more science journalists and other journalists to attend...

ME has been the first topic on Norwegian TV2's main news broadcast two days in a row. Tonight we met a family with a daughter with severe ME. They have been reported twice to the child welfare authorities. The contact person in the Norwegian ME Association for carers was interviewed as well as...

Another news section about ME from Norwegian TV2. 2 mothers to ME-sick children in the studio, as well as professor Ola Didrik Sagustad and the creator of yesterday's documentary, Pål Schaatun. Prof. Saugstad says that the knowledge about ME varies a lot, but is improving. However, many...

Agree! I noticed however that Lightning Process coach Live Landmark is complaining on Facebook that she and several others with a biopsychosocial approach had been in contact over a long period with the journalist behind the documentary. Several of them were filmed/interviewed, but were cut...

The documentary about ME and RituxME that was sent tonight on Norwegian television was amazing. No big news revealed, but presented the disease very respectfully, had a lot of information and gave good insight to the researchers and their work at the cancer ward at Haukeland university...

Article about ME in connection to the documentary tonight about RituxME and ME on Norwegian television. TV2: Emilie (18) har ligget i senge sammenhengende i ti måneder google translation: Emilie (18) has been lying in bed for ten months Includes statements from prof. Wyller who actually...

This #OMFScienceWednesday post definitely deserves its own thread :emoji_confetti_ball::emoji_clap::party: OMF creates as new Harvard ME/CFS Collaborative Research Center and expands Stanford Data Center We are proud to announce that OMF has funded $1.8 million for the establishment of a new...

Trailer for tomorrow's ME-documentary on Norwegian television. The documentary has followed some ME patients and the RituxME trial for two years. It will be aired on TV2 tomorrow at 21.40. Here is the documentary's Facebook page.

Thanks once again, @Andy for helping out. I keep forgetting that there are alternatives to google translations..

Article in the Swedish newspaper Aftonbladet about 13 year old Irma who has ME. It explains very well her isolation and the family's frustrating meeting with the health care system who lacks knowledge about the disease. Aftonbladet: Irma, 15, lever med obotliga sjukdomen: "Det är så jobbigt"...

- I’ll be damned to see another few generations of promising dancers, artists, athletes etc. being wasted merely because of politics. It needs to stop. My hope is that patients and allies will have the strength to keep telling the truth about this disease until we need to do no more. We are...

Excellent opinion piece from Sweden Metro: Agnes Arpi: Okunskapen om ME-sjuka är tragisk google translation: The ignorance about ME patients is tragic The fact that the body and the brain is connected is true, but the statement "it's in the head" is terribly misused. So many patients, meeting...

They already did :laugh:

Yes, I think it is safe to assume they might have been somewhat ... eclectic... in whom they've reached out to. :whistle:

Found it and it was a breeze! Just click here and find the location of your event on the list, click on the link and upload. They want pictures from physical events, not virtual. SmugMug City Upload Links (#MillionsMissing 2018)