By Valerie Eliot Smith.
Regular readers of this blog will already be familiar with Karina Hansen’s horrifying story (as detailed in my series of posts) and with the often appalling treatment of myalgic encephalomyelitis (ME) patients generally. For new readers, and those needing a more detailed reminder of her story, there is a full summary at the end of this post.
Karina is a young woman from Denmark who became ill with the severe form of ME as a teenager. She was being cared for at home by her family but, in February 2013, she was forcibly removed by the state authorities and confined in an institution for three and a half years as a de facto psychiatric patient. Her family members were not allowed to visit her and she was subjected to highly inappropriate treatment.
She was eventually allowed to return home in October 2016, in a far worse condition than when she had arrived at the institution. Both she and her family have experienced – and continue to experience – considerable trauma as a result of this state intervention.
I have recently received an update on Karina’s situation from Bente Stenfalk of Borgerretsbevægelsen (Civil Rights Movement Group in Denmark). Bente has been closely involved in Karina’s case since 2015. I have paraphrased Bente’s statement (with her permission) for clarification purposes. It does not make for reassuring reading:
To read the rest of this story, click on the link below: