The first Neuralink implant in a human malfunctioned after several threads recording neural activity retracted from the brain, the Elon Musk-owned startup revealed Wednesday. The threads retr…
The first Neuralink implant in a human malfunctioned after several threads recording neural activity retracted from the brain, the Elon Musk-owned startup revealed Wednesday.
The threads retracted in the weeks following the surgery in late January that placed the Neuralink hardware in 29-year-old Noland Arbaugh’s brain, the company said in a blog post.
This reduced the number of effective electrodes and the ability of Arbaugh, a quadriplegic, to control a computer cursor with his brain.
“In response to this change, we modified the recording algorithm to be more sensitive to neural population signals, improved the techniques to translate these signals into cursor movements, and enhanced the user interface,” Neuralink said in the blog post.
The company said the adjustments resulted in a “rapid and sustained improvement” in bits-per-second, a measure of speed and accuracy of cursor control, surpassing Arbaugh’s initial performance.
While the problem doesn’t appear to pose a risk to Arbaugh’s safety, Neuralink reportedly floated the idea of removing his implant, according to The Wall Street Journal.
The company has also told the Food and Drug Administration that it believes it has a solution for the issue that occurred with Arbaugh’s implant, the Journal reported.
The implant was placed just more than 100 days ago. In the blog post, the company touted Arbaugh’s ability to play online computer games, browse the internet, livestream and use other applications “all by controlling a cursor with his mind.”
Agreed. I was flippant after reading the headline, since I don't like Musk, but once I read the story I was like "oh yeah this tech does have big potential for the differently abled. "
A quadriplegic being able to control a cursor on a screen with the implant for 100 days seems like a legit first attempt.
Could be great for the accessibility movement in the long run. But I could be naive or too optimistic.
Yeah I feel like it’s an attempt to resolve the Deaf stance that deafness isn’t a disability. The general stance of the Deaf community is closer to that of the queer community than that of say the paraplegic community. It sees deafness as a disability constructed by a society unwilling to communicate visually and to teach signed languages to all people able to use them.
Mind you we’re the contentious portion of the disabled world. The Deaf are as bad as lesbians I tell ya.
But on point, “differently abled” feels like it washes away the struggle. I am disabled. I’m disabled by a society that taught my great grandparents, my grandparents, and my parents not to teach their hard of hearing children sign language because otherwise we won’t use English. I’m disabled by a society that doesn’t include visual signals in emergency sounds even when it’s easy to do. I’m disabled by a society where people, including cops, will speak to the back of my head and not even consider that I didn’t respond because I didn’t hear. And I’m disabled by the assumption my life has to be worse for having less sound as though I’m not extremely literate and completely capable of using a signed language. I’m not “differently abled” I’m completely able in most ways everyone else is, and people who can’t learn to communicate visually are just as disabled as people who can’t learn to communicate audibly.
The deaf argument is that there’s no need for assistance of assistive tools. An all deaf town would experience no undue hardships unlike an all blind town.
I’m personally on the fence about it, but trust me when I write that we’ve seen whatever your gut instinct on this is before. Your gut take is just a hearing person speaking against Deaf theory written by Deaf people and the people far more involved in it are probably not going to see it because the Deaf don’t deal with the hearing as much as other disabled groups do, for obvious reasons.
How do people who have gained hearing feel about it? It seems like hearing would be important for a number of things besides communication, but maybe modern life doesn't require much?
Yeah, you can build it up, but it’s unpleasant and slow and idk if it can get all the way.
Basically (from what I remember/understand) your body loves “use it or lose it” on anything resource intensive, and nothing uses resources like brain. So if you aren’t getting sound you let other stuff butt in on that area and you never build up auditory processing. Add in the fact that CIs don’t work the same as biological cochleas (seriously there’s videos with sound replicating various CIs) and you basically have to relearn how to hear.
Another connection is actually autistic people with issues with verbal communication often don’t have those issues with sign language. It’s processed differently but not in a way that makes it super hard to learn, it’s honestly easier to pick up than most languages.
Because they kinda suck in a way wheelchairs don’t. Wheelchairs grant an alternative to ambulation. Cochlear implants give a new sense, one that those born without it literally don’t have the brain buildup to deal with. Like, look into those who got it and don’t use it. And often they’re forced on children by parents who will never learn sign language. I’m on board with children getting CIs as a teenager if a mental health professional with expertise in the deaf signs off that they weren’t unduly coerced, but it’s a major medical decision often forced or coerced on infants and young children by hearing parents and a hearing society to serve the interests of the hearing rather than the deaf child.
Fucking hell, hearing aids are uncomfortable. And not just because it’s something inside your ears. Like, it’s not the same as natural hearing (my loss is degenerative, I’ve had both). The sound filtration is worse and it overstimulates the brain. But hearing people get angry when you turn your ears off because you need a break because to many hearing people the point is to make you not deaf/hard of hearing. But the fact is we always are, it’s just that sometimes we’re using an assistive device that is often uncomfortable or outright painful.
Cochlear implants might be better seen as a lesbian having a platonic husband instead of a romantic wife. It’s uncomfortable assimilation and a worse solution in the absence of social pressure, and it gives the pressure ammunition. Absent the social pressures, it’s your choice. And to be upfront, I expect to get them once my hearing reaches the point they’re better than hearing aids. And also if I was a native signer they would have to earn a place in my skull and I’m angry that I’m not a native signer. As I implied, my hearing loss is genetic, and it fits pretty well to what your middle school taught you about a mono-allele dominant trait.
Wheelchairs are often seen as liberating to their users. Hearing aids and cochlear implants are often seen as burdens to their users. Nobody has to punish their child or nag their spouse into using their wheelchair, but for hearing devices, it’s common, it’s expected, it’s something you’re warned about beforehand. Please be understanding of the Deaf, we may not always be the nicest or easiest to understand, but nobody understands deafness better than us.
Actually in the wheelchair community, there can indeed be pressure to use the least assistive wheelchair possible. Chairs aren't 100% seen as liberating and there's a lot of nuance into why people pick certain chairs beyond finances. My aunt repeatedly fell out of her chair because she insisted on one made for a lower back injury than she has. She kept it for status, because she looks more able without the sides.
I guess 'differently abled,' just comes across as ableism to me. Not using visible signs of a disability, like a chair or hearing aids, can be internalized ableism. Some of the worst verbalized ableism I've heard has come from disabled communities. It's a very complicated topic, not least because disability is used to harm disabled people and take away their agency. And for many, there is a lot of grief with using assisitive devices.
That being said, I don't think people should be forced to change or to use devices they dislike. My aunt still uses her chair, it's not like we're going to drag her into another one or whatever. I just wanted to point out the internalized ableism that could be contributing to this attitude and word change.
It wasn't so long ago that the Civil rights Era stopped disabled people from being chained in attics and lobotomized and hid away. It's entirely reasonable to fear that association.
Had a class with some ABA techs who gave a presentation about Autism Speaks for their final project - they had no idea that criticism of AS/their entire field existed.
It’s hard to get away with “your presentation and profession is shit and you didn’t bother looking into any information other than your first google search” as a peer unfortunately. I did manage some gentle questions about AS’s one autistic board member’s exit….
It is fascinating that “behavioral health” seems to be just torturing/drugging kids until they get “better”/learn to comply. I didn’t get ABA, but very similar treatment.
it's not really that fascinating, of course the cheap and easy answer is a derivative of "beat it until it behaves", a large part of the states still have the paddles in school
I get that there are better choices now, but let's not pretend like a straw you blow into is the technological stopping point for limb-free computer control (sorry if that's not actually the best option, it's just the one I'm familiar with). There are plenty of things to trash talk Neuralink about without pretending this technology (or it's future form) is meritless.
I feel like I’m going nuts, is eye controlled adaptive tech really that obscure? We’re not talking about maybe letting people walk again or giving them otherwise unattainable control over a computer, we’re talking about a different mouse input. The risks should be proportional to the gains.
Can you take a moment and imagine some possibilities of taking input directly from someone's mind and applying it without needing to use your body? I know moving a mouse doesn't seem impressive, but it demonstrates success at a technological concept that still seems impossible. I can't speak for the ethics because I don't know how voluntary the subjects are for the research, but this is very exciting for me, because it will inevitably become more sophisticated.
Cool, when you can upload your thoughts somewhere we’ll be having a different conversation about its risks and uses. But what’s happening right now is that they did brain surgery on a man to let him move a computer mouse.
I don’t accept that disabled people must be sacrificed at the altar of Progress, and I think the entire process for how they recruit patients and explain the capabilities and risks of the implant deserves extreme scrutiny. There’s a reason doctors have to get hours of education in ethics to be considered competent, it’s a lot more complicated than “just do whatever if it can technically work for a bit.”
Is it worth risking dying to be able to move a mouse slightly faster than you can move your eyes and blink? If your answer to that is yes that’s your body, but I think it’s important to contextualize that the options here aren’t brain implant or nothing.
Why not? Nothing wrong with research and development as long as everyone participating in the test is an informed, consenting adult IMO. The advancements could make current accessibility tech even better. For one reason or another, a quadriplegic person decided they were willing to take the risk, so maybe they consider current accessibility tech for quadriplegics to be insufficient and wanted to try for something better?
Please dude I promise you this is near universally hated by disabled people 😭
I cannot speak to any of these, however, I learned that that you should just ask. If you can’t ask, put the “human” first such as people with disabilities or people who are deaf, blind, etc. Latine is another term I’ve heard, but in the community, there are those that like it and those that don’t.
What you said is often true but not always. Some communities prefer person-first language, some prefer identity first language.
For example, generally speaking, "autistic people" is preferred over "people with autism". The reasoning being "this is just part of who I am, it's not an affliction that I have."
I'm not autistic but I have lots of friends who are, and they all prefer to say "I'm autistic" rather than "I have autism".
Like you said, it's best to ask, or just copy the language that the person uses for themself.
When a company stops supporting devices like this, the devices and their documentation and code should be required to enter the public domain. It should not be allowed for assistive devices to become e-waste stuck in a patient's body.
Of course it is. The what neuralink is touting is the exact same situation that company was in. What happened there was they were creating an application for types of rare retinal blindness with the hopes that some other research would magically come along that makes it apply to other types of blindness and give them a market they could properly scale in. Surprise Surprise, no such deus ex machina occurred and the company could not see a path to profitability.
Neuralink is the exact same, cervical vertebra paralysis has less invasive adaptive mechanisms that are cheaper to implement, so there's no way this will ever be a profitable approach with that alone. They're hoping that this will magic into some brain machine interface without any actual hope that is going to happen.
The basic research just isn't there to be doing this shit, but the investor dollars need to be put somewhere.