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Category Archives: Finland

Announcing #MillionsMissing 2019! Join us!

Listen to the article: We are thrilled to announce #MillionsMissing 2019! This May, we will take to the streets - or demonstrate from our beds - to show the world we are here, we are the #MillionsMissing, we will continue to fight for our demands for people with myalgic encephalomyelitis ...

A Year in Review: Celebrating the 2018 Achievements of Our Community

2018 has been a big year at #MEAction!  Thank you to all of you who have put forth immense efforts to improve the lives of people with myalgic encephalomyelitis (ME). #MEAction has grown over the past year in leaps and bounds, and we cannot wait to do more. We will not ...

Advocacy Round-Up: End-of-Year, 2018

Our community's advocacy work end with a big finale with our meeting with the director of the U.S. National Institutes of Health (NIH)!  Catch up on the latest global news from the past few months. U.S. NIH #MEAction representatives met with the National Institutes of Health (NIH) director, Dr. Francis Collins, ...
boy in bed with arms folded and head lowered

Suomalaisen Äidin Kertomus

Suomalaiset ME/CFS-potilaat tarvitsevat apuasi. Allekirjoitathan vetoomuksen! Editorilta: Klikkaa tätä lukeaksesi englanninkielinen versio artikkelista. Editor’s note:  Click here to read the English translation of this article. Kaksitoista vuotta sitten syntyi poika, nuorimmaiseni. Iloinen hymyhuuli nauratti aina muita vitseillään ja oli kaikessa innolla mukana. Koulu oli kivaa, samoin urheilu ja kavereiden kanssa leikkiminen. Elämä ...
boy in bed with arms folded and head lowered

The Story of a Finnish Mother

People with ME/CFS in Finland need your help. Please sign their petition! Editor's note:  Click here to read the Finnish translation of this article. Twelve years ago a boy was born, my youngest. A happy, delightful child, always making others laugh and enthusiastically participating in everything. He liked the school ...