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.”
I agree with not liking ‘differently-abled’ as a term. To me it reads along the same lines as ‘disabled people are built different’. Pretty awkward.
Not that I have a horse in this race. Or a neuralink, as the case may be.
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.
That’s like saying blind people are not disabled, it’s just society that insists on visual stimuli
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?
There’s a variety of opinions. Born deaf often don’t like it. The later deafened you are the more you tend to want hearing back.
It’s not even about the communication per se, it’s also about the physical act of hearing which can be uncomfortable
That’s interesting. So if your brain isn’t developed to cope with hearing, it’s overwhelming similar to someone with autism?
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.
Deaf people and hard of hearing people may be more likely to be involved in car accidents
https://journal.nafe.org/ojs/index.php/nafe/article/view/27
My aunt and uncle are Deaf and contentious is pretty accurate.
I get why cochlear implants are shunned, but I don’t get why it’s such a hot button to even consider. We give paraplegics wheelchairs y’know
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.
I mean people are surprised that autistic people dislike autism speaks
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.
oh, ABA, you mean the “therapy” that for some reason causes a suicide rate of over 70%?
tho an “ABA tech” is cheaper than an actual medical professional since they just need a few weeks of training instead of several years
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
In the states? At least in mine, parents have to give permission for the school to paddle. Most districts don’t want the liability or the paperwork. At least in public ed.