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Abortion is a Disability Rights Issue – and Not Just Because of Eugenics

TW: Abortion, eugenics, sexual assault/rape.


Unless you’ve been living under a rock for the last week or so, you’ll have heard about Texas’s bill banning abortion after the sixth week of pregnancy – before most people even know they’re pregnant. If you don’t live on Twitter, though, you may have missed eugenics creeping into the debate.

A tweet from Richard Hanania of the Centre for the Study of Partisanship and Ideology points out that you generally can’t screen for Down’s syndrome before about week 10 (the NHS says you can screen for it and Edwards’ and Patau’s syndrome between weeks 10 and 14), and that lots of those who find out their child may have Down’s choose not to continue with their pregnancies. 

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‘Lacking in transparency, ethics, and compassion’: NICE pauses publication of ME guidelines

When NICE paused publication of the new ME guidelines this week it rocked the community that lived with the condition. Danielle Watts discusses why the harmful treatments some professionals are opposed to cutting out can’t be allowed to continue.

When Daniel Moore was a child he developed myalgic encephalomyelitis (ME). At the time ME was often described as ‘yuppie flu’, thought mainly to affect the middle-classes and to be a symptom of laziness rather than any serious illness.

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“Freedom Day” is Anything But for the Disabled and Vulnerable

So, it’s now “Freedom Day”. After watching people attack disability activists for supporting the delay this last month, here it is. I watched last week’s Downing Street briefing from behind my fingers. The Prime Minister stood there ignoring all of the figures. Chris Witty and Patrick Valance flanking him, giving his b*llocks an air of respectability. Both of them appearing to be trying their very hardest not to outright say “I don’t agree with this decision.”

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NICE’s Worrying New Chronic Pain Guidelines

It’s the summer of 2012. I am still at university, using the very last of the term-length pool membership I’d bought. I swim 2 miles. That’s 128 lengths of a 25m pool. The walk back up to the main campus is hard, steep and my bag is heavy with my wet costume. I collapse onto my bed. My hands hurt, but four or five doctors can’t tell me why that is. My knees hurt, but after three doctors, I saw one specialist who said it should clear up by the time I’m 20, which I turned last month. I swallow a dihydrocodeine and sleep for 8 hours.

The NICE guidelines released on 7th April recommend analgesics not be used for primary chronic pain. What they do recommend is exercise, antidepressants, acupuncture, and psychological therapies. Paracetamol and ibuprofen, possibly some of the most widely taken drugs outside of penicillin, that usually cost about 20p for a box of 16, they also can’t recommend. 

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Introducing The Unwritten Disability and Abuse Survey

It’s been a tough few weeks for women, femmes and all those of marginalised genders who have experienced abuse at the hands of men.

Out of all of the hurt and pain however has come a new battle cry, a demand that we will not be treated like this again. But, unfortunately it’s something that disabled people have been largely left out of.

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Life and Anxieties as a Deaf Woman in the Wake of Sarah Everard’s Murder

TW: Murder of Sarah Everard, sexual assault/harassment concerns, victim blaming. There are links to places to find support at the bottom of this article.

I jump when my sister walks up behind me in the kitchen, then we watch my Fitbit as my heart rate comes down almost double because of the scare. I don’t know if my parents were scared about me growing up as a deaf young woman. They knew I was fiercely determined and were probably quite afraid to get in my way but I am moderately deaf and don’t hear footsteps, even those of the people I love most, even in the quietest of houses. 

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Please Stop Killing Us

It’s been an awful past 12 months, I don’t need to tell anyone that. For disabled people it’s not just been the threat of the pandemic that’s been weighing on our minds. Ever since lockdown was announced last year, disabled people were the first to be thrown under the bus and it hasn’t stopped.

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Sia’s ‘Music’ Golden Globe Nomination is a Stab in the Back for Disabled Performers

You may think that a film about a neurodiverse character being nominated for a Golden Globe is an incredible leap forward in terms of equality and diversity in the entertainment industry and you’d be correct, but Sia’s film ‘Music’ is rather the opposite. 

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The changes to the Mental Health Act are great for autistic people, but it’s not enough

TW: This post mentions institutional abuse of disabled people.

Recently, it was announced that the Mental Health Act would be facing some landmark reforms in order to tackle its discriminatory overuse against some of the most vulnerable groups in society.

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Free School Meals Private Contractor Refuses to Cater for Children With Dietary Requirements

By now you’ve probably seen what the government thinks constitutes for a week of meals adding up to £30, but just in case you don’t inhabit Twitter let me whet your appetite.