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i have a suggestion
Today in australia they started senate hearings on the bill the government hopes will make enough disabled people die or disappear to make us all less irritatingly expensive for them. We had two weeks to submit feedback on over 400 pages of complicated legal terms. They don't care what we have to say and they don’t care that this will kill people and disenfranchise disabled people across the country.
There are 760,000 Australians on the National Disability Insurance Scheme, the system that - if they feel like it and your personalised plan says you get to have it - provides funding for everything from personal hygiene care to support workers to therapies to assistive technology. It's already very hard for disabled people to get on the NDIS, regardless of your disability. It's near impossible to access most support and equipment without being on the NDIS. And the government has announced that they want that number to drop to 600,000 in four years. 160,000 of us cut off the Scheme - and countless more denied access. This will cause deaths. People will die and people will suffer because there is no safety net. The NDIS is the only option for most of us. Even private health insurance doesn't cover most of these things. Nobody will swoop in to save us.
The bill wants to give the (non disabled!) NDIS minister basically unlimited power to cut our funding. They're already planning what they'd do with that power. What rights they'll strip from us. What dignity and freedom they'll remove to make their budget look better.
The bill wants to force people to try every treatment out there before they're allowed to be on the NDIS. Including if the treatment is literally impossible to access. There’s a lot of us living in regional areas or out bush who can't just pop to the capital cities for specialists. This will especially hurt disabled First Nations people in regional and remote communities, who already experience limited access to healthcare. Oh, and it includes chemical restraint, too. The government has directly refused to exclude chemical restraint from the required process, calling it "trialling medication".
If you're australian and worried, the ABC did a good breakdown of the proposed changes.
I know australia stuff doesn't really pop up on the radar on this site, but I want everyone to know what's going on. What we're fighting for here. Your australian disabled friends might be NDIS participants fearing for their life, rights, and freedom. They might not be a participant and afraid these changes mean they never will have access. We deserve better. The government built a system with no backup plan, and now they want hundreds of thousands of disabled people to pay the price for their bad planning.
Sorry we're too expensive to have rights, I guess.
Some additions, from the notes and also context:
- Nobody needs to apologise for venting in the notes or reblogs. We're scared and upset and deserve to be heard.
What to do:
- australians: don't give up! There's still people fighting this, it's not law yet. And even if it passes we can fight them on it. Most disabled peoples' organisations are fighting this, so organisations like People With Disability Australia and area specific groups. Membership to most of them is free if you're disabled. PWDA sends out a list of the news about us each week to keep us informed.
🔗Disabled People Against Cuts are leading a charge. There's always a way to make politicians pay attention even if we have to park our arses on their front step. Share support and resources where you can and keep an eye on the others in your community if you're able to. Talk to local support clinics about Coles and Woolworths vouchers for those facing a lot of uncertainty. And get your flu shot if you're able. Nobody needs the next protest to give everyone the flu.
- non-australians: keep watching. You might also benefit from seeing what DPAC are doing and if they ever call for international support. Supporting the disabled australians you know and refusing to be kept in the dark about what’s being done to marginalised people internationally is good preparation for lots of ways to help, it means you're ready to go if something you can help with appears and don't lose time educating yourself. Many of the situations with the NDIS have deliberately had short time frames to act, to try and stop us from having a voice.
context from the notes:
- When I said health insurance doesn't cover disability supports, I don't mean "it's very expensive so people can't access it". I mean the services often won't take on anyone who doesn't have an NDIS plan. Even then, it's common for services to prefer people who are "plan managed" or "agency managed", meaning someone else handles our invoices, because they feel "self managed" people might not pay them fast enough.
- People have been getting "check in" phone calls from the agency. It’s secretly plan reviews for them to reduce people's funding. If they call you and you don’t have your support people with you, they are lying when they say you don't need them. Tell them to organise a time to call later so you can have your support people. This kind of warning is the only reason I knew to contact my support coordinator when I got this phone call. Others I have seen didn't know and got their plan cut. And it takes years to try and change a plan or appeal it through the tribunal.
- Someone in the notes has identified herself as a support coordinator and offered to help with questions for people concerned about their plan via DMs (thank you @andromedusia). This is very kind of her and I also hope mentioning this here doesn't cause you any trouble, very sorry if it does.
- Also, not thrilled to find out they might be phasing out support coordinators. Lots of us are dependent on them - a support coordinator is someone who helps us understand out plan and connect with supports, and often helps with advocacy too. They’ll save money on us purely because we won't know where to go or what the plans mean. They use a lot of confusing terms in the plans. I'd be screwed without my support coordinator.
- Oh they also want to use a standardised assessment tool to tell how disabled we are, after a decade of having to pay out of pocket for specialists who know us to provide reports. This is actually worse because the tool doesn’t have to be done by a qualified professional and doesn’t work on people with a lot of different disabilities. The government is very good at somehow turning "bad" into "worse".
- Yeah. 760,000 australians is actually not that many. There's 27 million people living here. 85% of disabled australians aren't on the NDIS. Now, a lot of disabled people don't necessarily need the kind of support the NDIS provides, but you know who I don't trust to make that decision? The government who doesn't want to pay for it.
- None of this fixes the existing problems with access for First Nations people or people from culturally and linguistically diverse backgrounds. I'm pretty sure a standardised assessment tool will actually only make that way worse. No room for professionals to work with cultural sensitivity and humility to understand the impact of someone's disability, or the varying ways First Nations communities may construct and talk about disability that don't necessarily align with the settler government's convenient definition. Just checkboxes.
- This isn't even our "conservative" government party in power. This is the centre/centre-left party, Labor. The 'Liberal party' (note: not liberal) would likely do worse. But I don't think there's much to be grateful for when this will kill people. And probably won't stop later conservative cuts anyway. Because we cost too much.
It means a lot to see people care about what's happening here. Thank you for paying attention and getting angry with us. Because we're angry and scared and have a right to be heard that the government is doing its best to not have to hear.
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“Eternal Presence” by John Wilson
Photographed by David Schafer
A planned community in Arizona has used time-honored Mediterranean strategies to keep temperatures down and attitudes high. Western civiliza
"A planned community in Arizona has used time-honored Mediterranean strategies to keep temperatures down and attitudes high.
Western civilization has grown remarkably climate conscious over the last 20 years, but not when it comes to building, civic planning, and especially zoning. Perhaps the interiors of buildings are becoming more climate adapted, and in some cases the facades as well, but in a way that’s a little like inventing a freezer designed to keep ice cream frozen while sitting next to a fire.
Wooden or concrete boxes arranged side-by-side across leveled ground with sprawling, largely treeless gardens and concrete sidewalks alongside wide, blacktop roads is simply a culture of construction that has to be abandoned if living in a world of 2°C or higher annual temperatures [or, hopefully, less than that, but nonetheless likely over 1.5°C] is to be tolerable.
Fortunately for Arizonans, change may have finally arrived in the form of a carless, planned community that looks and feels like a Greek island village.
In the Phoenix suburb of Tempe, Culdesac has arisen as a 17-acre mixed-use neighborhood from the ground up to stay cool and local, taking the concept of the 15-minute city, where anything a resident might need is only 15 minutes away, and putting a Mediterranean spin on it.
Buildings are tall, thick, and totally white. The residential areas look like they were built atop of the ashes of the Phoenix zoning code burnt in effigy. Crammed together, they create narrow streets and alleys that are almost constantly shaded, through which wind is channeled and accelerated in passing.
Windows open towards each other, allowing wind that enters one building to exit into another, while the total lack of asphalt means that the ground temperatures are a staggering 50-60°F lower than pavements beyond the limits of Culdesac.
No privately-owned cars are allowed to enter the neighborhood, in which electric bikes, robotic mini taxis, and light rail shuttle people around town, to downtown Phoenix, or out to the airport.
The street life is lively—there are no cars to bisect movement between the 21 different businesses and eateries, among which is a James Beard Award-winning Mexican restaurant, DIY ceramic business, and some stores run out of apartments—a big no-no under Phoenix zoning laws.
“Once you pull the cars out,” Architect Daniel Parolek who designed Culdesac, told BBC, “there’s so much more opportunity to make a vibrant, thriving community.”
His inspiration was sun-soaked locales like Italy, Greece, and Croatia, where town centers were designed before the automobile and before air conditioning.
Technically speaking, the entire Culdesac neighborhood is one apartment complex, but the paseos, or little alleyways, open up into plazas of open space exactly liked one would expect in a little village in the Cyclades.
Because no one has to jump in a car to get from place to place, people run into each other, sparking conversations, relations, and breaking through the counterintuitive phenomenon of big city loneliness, which in Phoenix hits particularly hard.
“Culdesac Tempe has shown that people do want to live car-free in the US, even in a metro area like Phoenix that’s often seen as the poster child for car dependency,” says Erin Boyd, Culdesac’s government relations and external affairs lead. “This success has shifted the conversation around what’s possible in American development.”
-via Good News Network, August 25, 2025

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it’s such a basic part of the reality of disabled people as a whole but it’s STILL so hard to get ppl to understand that some people will simply die without 24/7 care. their care is not for comfort, it’s not for fun, it’s literally a matter of life and death. “if their care was taken away i’m sure they’d learn to suck it up like the rest of us!” – something ive heard time and time again. no they wouldn’t, they would die. they HAVE died. they continue to die as cuts are made to welfare and health. why is this so impossible for people to grasp.

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