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Kera O’Regan Profile
Kera O’Regan

@keraoregan

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» Kāi Tahu » Social Impact Strategist » Facilitator + Speaker » Climate activist 🌏 » Disability & Indigenous Rights ✊🏽 » Papatūānuku 🌿 Same @ everywhere

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Joined October 2011
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@keraoregan
Kera O’Regan
2 years
I think a lot of people in social change spaces have a really colonial & extractive view of “community” where community = a group with shared characteristics that they can opt in or opt out of as it affords them utility and is a source of comfort.
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@keraoregan
Kera O’Regan
1 month
RT @holo_cene: update c’est ce dimanche ! pratiquement personne n’a pris de place depuis ce post 🥲💔.
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@keraoregan
Kera O’Regan
1 month
RT @holo_cene: last night i held the first ever mask-required covid-safer concert in france! everyone in the audience wore a KN95, and air….
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@keraoregan
Kera O’Regan
3 months
Whoever figured out that cold exposure & singing helps migraines is an absolute genius 🙌🏼. My neighbours may disagree, but it just saved me a trip to Emergency so I’ll call it a win!.
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@keraoregan
Kera O’Regan
3 months
RT @broadwaybabyto: All of these factors just make maintaining a baseline all the more important, but it is a delicate balance. Every thing….
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disabledginger.com
So why is it so hard to do? And how can we make it a bit easier?
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@keraoregan
Kera O’Regan
3 months
RT @broadwaybabyto: People think we’re isolated and lonely because we’re often housebound and unable to do the activities we used to do, bu….
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@keraoregan
Kera O’Regan
3 months
RT @broadwaybabyto: That each Covid infection is playing Russian Roulette with disability and eventually, your number will be up. There’s….
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@keraoregan
Kera O’Regan
3 months
RT @broadwaybabyto: so when the rest of the world decided to bury their heads in the sand and rush ‘back to normal’, we got left behind. S….
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@keraoregan
Kera O’Regan
3 months
RT @broadwaybabyto: There’s a ton of overlap between the Covid Cautious & Chronic Illness communities because people living with chronic il….
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@keraoregan
Kera O’Regan
6 months
RT @FinalSixth: @JamesThrot @JamesThrot so much 2 unpack in this thread. This pt may've already been made, but obvs the other GIANT link bt….
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@keraoregan
Kera O’Regan
6 months
But I do think that the question warrants research and looking into - I just think that needs to be done with extreme care and leadership from both disabled community as well as neurology and psych and sociology researchers etc. so it doesn’t reinforce ableism.
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@keraoregan
Kera O’Regan
6 months
Maybe people don’t have the financial/time/other resources to contribute as much to collective and positive causes. Maybe people are quite literally traumatised and struggling because there’s been no real support or recovery - just straight into “back to normal”.
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@keraoregan
Kera O’Regan
6 months
And I know I’m not the only one observing this. Of course it could all be explained sociologically - maybe it’s just that people are burnt out, or economically things are still tough since the early days of the pandemic so people are more in survival mode.
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@keraoregan
Kera O’Regan
6 months
need to put things in writing, or use accommodations / techniques I’ve learnt in collaborating with with friends and colleagues with learning disabilities on family members and friends who don’t consider that they have any long term Covid impacts.
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@keraoregan
Kera O’Regan
6 months
I am Covid cautious and seeing loved ones and others I know change with their 2nd, 3rd, 4th infection I *do* worry there are real challenges we need to face as a collective. I notice MANY peoples’ memory is far worse than it used to be - and am often shocked at how much more I.
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@keraoregan
Kera O’Regan
6 months
AND at the same time, as a disabled person who has had neurological symptoms (but not TBI or learning disability) from my other conditions as well as Covid, I do think there is a very real need to understand the long term impacts of Covid on our societal conscience and movements.
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@keraoregan
Kera O’Regan
6 months
It increases the ableism & barriers they have to face in society, and also stops us recognising their amazing contributions to our society and collective good - with mental health & brain disabilities having been the strongest allies & activists for positive change.
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@keraoregan
Kera O’Regan
6 months
It also causes harm to disabled people by reinforcing the disability = bad stigma - particularly for people who do have mental health and brain injury disabilities.
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@keraoregan
Kera O’Regan
6 months
It makes it easy for people to see themselves as apart from the problem “I’m a nice white person, I’m not like *those* nasty racist people. They’re cr*zy” = “I don’t need to think about my role in a racist & fascist society or consider how I might uphold this oppression.”.
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@keraoregan
Kera O’Regan
6 months
Both and. When people call fascism, racism etc. a “mental illness” or attribute it to brain injury it is grounded in ableist and negative assumptions about ppl with said disabilities AND it also avoids accountability individually and collectively.
@JamesThrot
James Throt MBBS, MD, PhD, FRCPath
6 months
Neurologist here. Brain damage/injury can, and does, cause problems w/emotional regulation & lability. It can diminish empathy, remove inhibitions, and cause significant alterations in personality. It can make people say/do inappropriate things they otherwise wouldn’t have.
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@keraoregan
Kera O’Regan
6 months
RT @mintyhiggins: Archives holds our family histories and our nation’s history and the Chief Archivist is guardian. I’m confident the Archi….
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