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Kamis, 12 Desember 2013

Is the market for augmentative and alternative communication (AAC) devices about to be bulldozed by the tablet revolution?

Is the market for augmentative and alternative communication (AAC) devices about to be bulldozed by the tablet revolution?

The ‘i’s Have It?
Is the market for augmentative and alternative communication (AAC) devices about to be bulldozed by the tablet revolution? Sal McKeown finds out…

At the annual conference of the national charity Communication Matters, Gary Derwent said the following: “My unscientific opinion is that iPads and Android devices will continue to increase in use in the field of AAC – and that ultimately, there is no long term future for ‘dedicated’ AAC [solutions].”

Gary is joint Head of Assistive and Rehabilitation Technology and Informatics Lead at The Royal Hospital for Neuro-disability (RHN), and is keen to see new developments in AAC for the 300,000 children and adults in the UK with specialist speech requirements. His argument is that while specialist devices may have more processing power, memory and storage capacity than iPads and Android devices, they are usually assembled using long-established designs and components – such as motherboards, processors and chipsets – that are increasingly outmoded, compared to the latest mobile consumer technologies.
PX _DSC2645

Right now, people with cerebral palsy, neurodegenerative conditions or autism are lucky if they can secure funding for a specialist device from a company such as Dynavox, Tobii Technology or Toby Churchill. The costs of bespoke equipment can be in excess of as much as £5000 – and with demand outstripping supply, some young people may be left, quite literally, without a voice.
In contrast, the combined expense of an iPad and a suitable app can be less than £500, potentially offering access to many people who would formerly have found AAC beyond their financial means. But can a set-up costing few hundred pounds really be a serious rival to a specialist, heavy-duty dedicated device?

In praise of tablets
iPads and Android tablets tend to be small, easy to carry around and therefore easier to use in bathrooms or cars, whereas the dimensions of bulkier devices can cause problems. The downside is that consumer tablet devices are also often slippery and easy to drop, though mounting systems enabling different tablet models to be securely attached to wheelchair frames have recently started to appear.

Tablets are attractive items of technology and modern status symbols; with the best will in the world, dedicated AAC devices are not intrinsically desirable. There is no stigma attached to using an iPad or Android tablet, and both types offer great freedoms. Imagine enjoying a meal out with friends – it’s possible to use an app to talk to others at the table, take photos, instantly upload those photos to Facebook, send a text to your family at home and call a taxi at the end of the evening – all from the same device. More to the point, your fellow diners may well be using the same type of device themselves.

Tablets and the apps that run on them are easy to get hold of. You can scour the web, place an order and have the hardware delivered your door, then download the app(s) of your choice within minutes of turning it on.

However, unless you are a qualified assessor, your choice of hardware and software may be very wide of the mark. Without a specialist assessment, many users may not be developing their communication skills as successfully.

Not a medical device
Tom Griffiths is a Trustee of Communication Matters, and works as an Assistive Technologist at Great Ormond Street Hospital alongside doctors, therapists and psychologists. Times have changed to the extent that the team may find that someone arrives for an assessment having already purchased an iPad. “Our job is to support children, parents and therapists in their decision making,” Tom explains. “The iPad is not a medical device and not designed for this market, so it is not always the answer to communication problems.”
PX Hannah_Florida_I15Mounted_Wheelchair
The team does, however, try to support ‘the whole person,’ and not just focus on one particular area. “Young people don’t just want to speak to someone in the same room,” Gary says. “They want to play games, access their curriculum and have a digital presence. We can suggest strategies and advise on suitable resources and apps, so the iPad can be a valuable tool for all these areas.”
Whichever device ends up being chosen, it has to be dependable. Screens and hard drives tend to be the weak points in most computers, but iPads and other tablets now commonly come fitted with scratch-resistant Gorilla Glass and solid state hard drives that can withstand a lot of shaking.
In some respects, newer tablets are fast becoming just as robust as specialist communication devices. Dedicated devices may be contained within good, rugged housing, but the reliability of their electronics can leave much to be desired. Things have been improving in that area, but there remain complaints that some dedicated devices spend a lot of time on the workbench.
So while a case could be made for the industry not needing dedicated devices, it does still need dedicated research to be carried out, so as to ensure that the next generation of communication aids are the best that they can be

Methods of access
Gary Derwent believes that the assessment and most of the support needed should come from statutory services and schools rather than suppliers, because an independent view is vital. Yet he also believes that suppliers have a crucial role in innovating and developing new technologies. The challenge, therefore, is to find a business model and a means of interaction between suppliers, commissioners and statutory services, so that people who use AAC can benefit from the latest innovations while at the same time receiving independent advice and the best support possible.
Tablets provide access to touchscreen technology, and in some cases can be linked to a keyboard, but many users require other ways to make their computer work. These alternative input methods can include a mouse, trackball, joystick, a stylus-sporting headband called a ‘head pointer’ and advanced switch scanning or ‘eye-gaze’ technology, whereby the computer will register what the user’s eyes are focusing on and interpret their blinking to act as a switch when making a selection.
This is one of the reasons why Paul Hawes, ‎Managing Director of Smartbox Assistive Technology, welcomes the continuing development of new Windows and Android tablets. He points out that with Apple’s technology, every application on an iPad – and to some degree, the operating system that underpins everything – is run in isolation. This means that you are less likely to get viruses or dreaded blue ‘crash’ screens when things go wrong – but it can also make it very hard to transfer information and data between apps, or from the iPad itself to another device.
“PC technology uses USB ports [and has a] a long history of supporting alternative access devices and programs that talk to one another,’ Paul says. “This means that no one is locked out of the technology due to having cognitive difficulties or physical disabilities.”

Gary Derwent in turn acknowledges that at present, there are several reasons why a dedicated device is the best option for many people – while noting that these reasons are likely to decrease over time. As newer, faster and more powerful iPads and Android devices continue to be developed, it’s entirely possible that the hardware and access issues experienced by people with AAC needs will be resolved by tablet manufacturers.

But whatever happens with regards to hardware, it seems that all the experts in the field are agreed that users must have access to specialist assessors, training and a good aftercare service if their needs are to be properly met.
PX steve
Steve Evans

Case study – “Life is not over till the heart stops”
This autumn, Steve Evans went to Goodwood to see the motor racing, Brooklands to see Concorde and enjoyed a Manic Street Preachers concert at the Shepherds Bush Empire. Steve has Motor Neurone Disease (MND), which has affected his speech and physical ability to the point where trips out require a lot of forward planning between the venue, his family and carers.
He was diagnosed in 2007, and although the condition seems to have plateaued since 2010, he is now at a stage where he cannot speak unaided and is unable to move without assistance. He uses The Grid 2 – a software application from SmartBox Assistive Technology, which lets him use a computer as a communication aid with voice output, operate Windows and access the internet, as well as send and receive emails and SMS messages. It also connects to some home automation hardware that he has had installed in his house, thus enabling him to remotely put on some music, alter the angle of his bed, change the room temperature, turn on lights and switch TV channels.

“For anyone with MND, eye gaze is the only option,” Steve says. “I deliberately got a system before it was essential, to allow time to modify things and practice using it before I was dependent on it.”

Complete control
Once he became proficient, Steve was able to use his computer for internet shopping, online banking and even share dealing. Now he can use PC-based remote access software to operate three other computers in the house, “That means I can sort out problems on my wife’s and kid’s computers, or configure network settings.”
Given Steve’s reliance on eye gaze technology, his needs cannot be met at this time by an iPad or Android device with accompanying apps. Moreover, he will require support from specialists to continue meeting those needs as they change, if he is to enjoy the best quality of life that MND allows. “We don’t have a cure for this deadly disease for patients like me,” Steve concludes, “but still I remain an optimist. Life is not over till the heart stops.”

You find out more about Steve by following his blog at www.steveevans35.blogspot.co.uk

Senin, 08 Juli 2013

Graduate Student's Proposal for Google Glass is Accepted by Google

Graduate Student's Proposal for Google Glass is Accepted by Google

A doctoral candidate in Penn State’s College of Education is working to make a new technology into a tool to assist people with disabilities. Sam Sennott applied to the recent Google Glass project, which was offering Google’s hands-free, wearable computer to researchers and consumers as a part of the company’s research and development.

Sennott said he was eager to apply for the new technology when he heard about it in 2012. He submitted his 50-word entry in February, and Google contacted him about a month later to invite him to join the program. He said he anticipates receiving his Glass this summer.

“The overarching goal is to use Google Glass as an accessibility tool for people with a wide range of physical, communication and cognitive disabilities,” said Sennott.

There are three primary areas that Sennott identifies as possibilities for this project.

“First, will be helping people who struggle to speak by working with Glass as an augmentative communication tool,” said Sennott. “Second, will be to develop a range of assistive technology solutions. Third, will be looking at how parents, teachers and other related service providers can use Glass to enhance their work with students.”

Hacking things together to make them work is what special educators do on a daily basis, according to Sennott, so coming up with a new way to use Glass was natural.

“It is in my DNA to make solutions work out of whatever materials are available and to seek out new tools to get the job done for the students and families we serve,” said Sennott. “For me, all it takes is being with the individuals I serve and the ideas start flowing. I am committed to harnessing the power of innovative new consumer technologies to make a difference.”

This is not the first time Sennott has adapted a new technology to be used as an accessibility tool. He was able to collaborate on creating a popular technology for iPhone, iPod touch and iPad.
“I co-created the original Proloquo2Go,” said Sennott, “the iOS software that helps people who have difficulty speaking due to disabilities such as autism, cerebral palsy and developmental disabilities.”
Sennott anticipates that the assistive technology community will support this project.

“The assistive technology community is incredible,” said Sennott. “They mobilize quickly and are really generous with lending a hand to share about important new developments in the field.”
Sennott, who will be joining the faculty of Portland State University this fall, said he plans on using Google Glass as a part of his research in his new position, but he is cautious about his predictions for this project.

“My hope is that it provides tools that are powerful, discrete and always nearby,” said Sennott.

Kamis, 27 Juni 2013

For a Nahant family, life goes on with ALS

For a Nahant family, life goes on with ALS

 Via Boston Globe: http://www.bostonglobe.com/metro/regionals/north/2013/06/26/for-nahant-family-life-goes-with-als/EsGFyFBArgXF7i86T715UN/story.html

 
   George Mazareas, his wife Cynthia Mazareas, and their daughter, Elni Mazareas in their living room.
Matthew J. Lee/Globe staff
George Mazareas, his wife Cynthia Mazareas, and their daughter, Elni Mazareas in their living room.


NAHANT — George and Cynthia Mazareas are not living the life they had pictured when they got married in Greece 15 years ago.

When they started building a home in Nahant in 2000 and Cynthia got pregnant, they were looking forward to all the possibilities of the future.

But in 2003, George, now 53, was diagnosed with amyotrophic lateral sclerosis, also known as Lou Gehrig’s disease, and the couple’s life changed forever. By 2005 he had to start using a feeding tube. By 2006, he needed a ventilator to breathe.

Cynthia Mazareas, 49, said her husband’s illness has led them to redefine what they want out of life.
“For a while we probably felt like we were giving up on a lot of the things we had dreamt of and hoped for as a married couple and as parents,” she said. “I think now that we’ve sort of come to terms, it’s more like rewriting the story. It’s a different story than the one we had imagined, but that doesn’t mean it’s not a quality story.”
‘I think now that we’ve sort of come to terms, it’s more like rewriting the story. It’s a different story than the one we had imagined, but that doesn’t mean it’s not a quality story.’ Cynthia Mazareas
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Today, their home is mostly quiet, except for the hum of the machines that keep George alive. A former athlete who was active in community affairs, the Lynn native now sits paralyzed in a wheelchair, his movement limited to facial muscles. His daughter, Eleni, now 10, has never known his voice.

On Monday, the Mazareas family, joined by about a dozen friends, traveled to New York City to accept the Courage Award from Prize4Life , a nonprofit that works to find treatments and cures for the disease that took former governor Paul Cellucci ’s life earlier this month. There, Cynthia Mazareas delivered a speech on behalf of her husband, who spent weeks writing it when he was more capable of using a computer.

During the last decade, the Mazareases said, they have raised more than $1.5 million for the fight against ALS through events they were either involved with or inspired. However, Thomas Leavitt, Prize4Life chief development officer, said the Mazareas family earned the Courage Award not because of fund-raising, but because of their resilience, spirit of hope, and unwavering dedication to each other.

“The physical intimacy of their marriage would decline,” Leavitt said, “but they weren’t going to change their emotional intimacy or the relationship with their daughter, which was a big impetus to continue living the lives they’re living.”

Amyotrophic lateral sclerosis , also known as ALS, is a neurodegenerative disease that rapidly robs a person of the ability to initiate and control movement and eventually leads to paralysis. According to the ALS Association, this muscle atrophy leaves patients with an average life expectancy of two to five years. This year marks 10 years since George’s diagnosis.

Mazareas said that while she and her family would go on stage to accept Prize4Life’s honor, she shares it with everyone who has stuck by their side while George has progressively lost physical abilities.

“It’s very hard for some people to see that, and that’s where courage comes in,” she said. “I think our friends are as worthy of a courage award as we are. They’re not afraid to look into the face of ALS and deal with it.”

For George Mazareas, his participation in ALS charities like Prize4Life and The Angel Fund stems from a determination to help find treatments and cures.

Elni Mazareas took a picture of her dad with their family dog, Bailey.
Matthew J. Lee/Globe staff
Elni Mazareas took a picture of her dad with their family dog, Bailey.

“For me, it’s very emotional because I think of the PALS [people with ALS] that have gone before me and passed away — and I have known about 30 people — then I think about all the future ALS patients, and I feel a duty to do my part,” Mazareas communicated through his wife.

Since he started using a breathing tube, Mazareas cannot speak aloud. He communicates with his family with a numbers and letters system, a language Eleni learned as a Father’s Day present when she was 5.

To start, George mouths a number, 1 through 8, each indicating a specified series of letters, words, or numbers. The speaker starts reciting the series, waiting for George to blink, meaning they’ve reached the correct letter. They repeat the process until words and sentences are formed. Sometimes George looks away instead of blinking, a sign that a letter or word was miscommunicated, and they start over.

“George says that this is one of the best things I ever did for him, finding this communication device,” Cynthia said, adding that after rows one through five were established, George added a sixth (“who, what, when, where, how, why”), seventh, (“new word”), and eighth (numbers 0-10).

Despite the emotional challenge of seeing her husband in this condition and the patience required to communicate with him, Cynthia said he is still very much her partner in marriage and parenting.
“George is the big picture thinker, the visionary, and I’m more of the executor,” said Cynthia, an attorney. “He’s still my go-to person in life. George still does a lot of the big thinking in the house and gives me a lot of good advice and guidance and direction.”

For Eleni, her dad is the man who taught her about Marvel comics and Harry Potter, and like any other father and daughter, sometimes they butt heads.

“Never argue with him because you’re probably going to lose,” she said with a smile.

Cynthia said Eleni has picked up on her dad’s strength.'

“She’ll say, ‘The thing I’ve learned the most from my dad is you can get knocked down, but you can get back up again.’”

Senin, 25 Maret 2013

Boston Children's Hospital model for patients who are Communication Vulnerable

Boston Children's Hospital model for patients who are Communication Vulnerable

A MUST read/watch for any healthcare professional working in a hospital, nursing home, etc...

The Boston Children's Hospital service delivery model for patients who are Communication Vulnerable was recently highlighted in the AAC-RERC spotlight on Supporting Effective Patient-Provider Communication Across Health Care Settings


http://www.childrenshospital.org/clinicalservices/Site2016/mainpageS2016P15.html

Kamis, 28 Februari 2013

Mobile Device for Augmentative Communication: Insurance Style

Mobile Device for Augmentative Communication: Insurance Style

Via IPAT ND Assistive Technology Blog

http://ndipat.org/blog/mobile-device-for-augmentative-communication-insurance-style/
 
NovaChat 5 & 7An Android or Apple mobile device with a communication app for people who have difficulty speaking, such as an iPad with Proloquo2Go, is not a new concept anymore. However, insurance paying for a mobile device with this type of software is not as commonplace. A little over a year ago, Saltillo came out with the NovaChat, a Samsung Tablet and/or Media Player enclosed in a hard-shell case with an external speaker and a sophisticated communication app for both children and adults.
The NovaChat comes in a “dedicated” model, which means the device can only be used as a communication device and all of the “tablet” features such as access to games, Hulu+, and internet are locked to the user. When a device is “dedicated”, it is considered appropriate for coverage by some insurances, state Medicaid programs, and Medicare. These particular devices currently fall under HCPCS code E2510 for billing purposes. Once the person has the device in their possession, they can purchase an unlock key from the manufacturer, which is not reimbursable by insurance, and have access to all of the features of the tablet.

The NovaChat comes in three sizes based on Samsung’s 5,”, 7″, and 10″ tablets. The 5″ model can be accessed by the touchscreen, while the 7″ and 10″ models also allow for 1 & 2 switch scanning. Check out these YouTube videos of everything from the clothes dryer test (Don’t try this at home!) to how the device actually works.
From the app to the case, the NovaChats are definitely worth consideration when looking for a communication device.

Rabu, 27 Februari 2013

ALS gives me patience

ALS gives me patience

Nell Hardy writes a montly blog about living with ALS.  This article is about using her communication device to engage in conversation with her friends and family.  Very impactful.
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Via GoErie.com


A group of women met at my house two weekends ago for a silent retreat. They surrendered commitments, cell phones and schedules for six hours. Gingerly, each woman dipped a toe or fingertip in the quiet before immersing themselves in the silence.


I patiently waited for them. I've been speechless for more than a year after amyotrophic lateral sclerosis put me in the ring with pneumonia. I lost and a tracheotomy was performed so I could breathe.


Actually I won because I didn't die, but who's counting?


In the months before the tracheotomy, my words were so garbled that only my sons and a few aides could understand me.


As the muscles in my tongue and throat atrophied, my speech became unintelligible. It wasn't much of a stretch to go from struggling syllables to silence. Sometimes it was even more difficult to no longer laugh or sing.


I tried different speaking valves to coax words out but none worked. Difficulty swallowing, inability to form words and stiffening limbs seemed a trio destined to take me down.


But I'm the runt of the litter. I'm plucky and come from a long line of strong Irish women. I'm determined to savor what my life offers.


Enter secret weapon, stage left. A portable computer called a Dynavox is my main ally in coping with ALS. Attached to my wheelchair, the computer has a screen with letters I choose by blinking at them. Then I select "speak" and words roll forth, framed by a voice of my choosing. Before my voice began changing because of the illness, I spent hours banking my words.


By saying nonsensical phrases such as "a blueberry perched on my pot of ink," the program tried to capture the frills and thrills of a human voice. For me, it fell flat. My words sounded like a different language uttered loudly in a tin can.


A conversation using the Dynavox is, well, different. It simply takes time. On a good day I can eye-type eight words per minute. That's when all variables settle nicely and the Dynavox stars align. Conversing with me involves silence and long pauses. I love the golden layers that quiet spreads between words and phrases.


Speaking through a device presents unique difficulties in our hasty, quick world. I travel at 10 mph in an 80-mph world. Often I finish a sentence only to find the conversation is three subjects ahead.


Others do not like silence; it doesn't fit in our hurried, worried world of instant answers. One friend is a coin jingler. The longer he waits, the deeper his hand plunges into and sifts through a pocketful of change. Others clear their throats, tap toes or actually sidle behind me to read what I type.


Sitting comfortably in silence wasn't always this easy. Before ALS I was a stuffer; I crammed soccer games, child care, horse shows, friendships and self-help into my life.


I wished for a new car, another horse, low-maintenance sons. Rarely did I stop for fear my life would catch up.


But sometimes it takes a crisis to evoke change.


Because of ALS I have downsized, condensed and decluttered my life. I'm finally patient in an impatient world.


NELL HARDY, of Fairview, writes monthly about her battle with ALS, also known as Lou Gehrig's disease (nhardy1@mydvox.com).

http://www.goerie.com/article/20130227/OPINION08/302279994/Nell-Hardy%3A-ALS-gives-me-patience

Kamis, 31 Januari 2013

Gleason spreads ALS hope with help of new technology

Gleason spreads ALS hope with help of new technology

Via NY Post


NEW ORLEANS — Conference Room 1 on the second floor in the New Orleans Convention Center was packed with reporters and photographers yesterday afternoon, jockeying for position to yuk it up with Jack and Jackie Harbaugh about which of their sons they want to see win Super Bowl XLVII.
Next door in Conference Room 2, the crowd was sparse by comparison, but the content was more powerful than anything that has or will take place in this hype-a-thon Super Bowl week — and that includes 49ers-Ravens Sunday in the Superdome.

Former Saints defensive back Steve Gleason, in the second year of his battle with ALS, sat quietly at the podium in his specialized wheelchair alongside his former New Orleans teammate Scott Fujita and a number of other supporters to Gleason’s cause.

Associated Press
THEN & NOW: Steve Gleason was the picture of health as a Saints safety during his career from 2000-07, but now at 35 he needs a wheelchair fitted with a special computer that allows him to communicate.
 
Gleason’s cause is about stopping ALS from becoming a death sentence to him and the many others afflicted with the cruel disease.

Using the power of Super Bowl week in his hometown of New Orleans, Gleason — just 35 — introduced the Team Gleason House, which will provide the state-of-the-art technology that allowed Gleason to communicate in yesterday’s press conference.

“What ALS takes away technology can give back,’’ Gleason said yesterday.
He said this not through speech from his mouth, but over a speaker connected to a computer screen that has a keyboard for Gleason to type in his thoughts. Gleason, who no longer has use of his hands, types with his eyes.

The new technology allows ALS patients to lock their eyes on a letter long enough that the computer recognizes it and types it in.

Watching and listening to Gleason speak of this new technology had a profound emotional effect on me. I lost a friend to ALS in June 2011 — Larry O’Rourke, a sports writer colleague who was everybody’s friend.

It was when Larry — whose lifeblood was his social contact with friends — was bed-ridden and on a ventilator, unable to speak or use his hands to communicate with friends via the computer that he asked his parents to turn the switch off and let him die.

If back then — less than two years ago — Larry had use of the advanced technology that Gleason has today and is promoting through his Team Gleason House, he could be here at this Super Bowl live-blogging and Tweeting his humorous musings.

That made speaking to Gleason yesterday both uplifting and sad, because it’s simply not that long ago when Larry faded quietly and died, as Gleason puts it, because of the lack of technology.
In the same way, being around Gleason yesterday invoked conflicting emotions. It’s sad seeing a once active NFL player so weakened by the disease, yet overpoweringly uplifting seeing what he’s doing with it.

“Every morning when he wakes up he always says he’s got to make a choice whether to be depressed and stay in bed or choose happiness,’’ Gleason’s wife, Michel, said. “And every morning he chooses happiness.’’

Long before this courageous public fight of his, Gleason was a hero in New Orleans.

It was his blocked punt early in a Saints rout of the Falcons in September 2005 at the Superdome that brightened lives in New Orleans, because it was the first home game since Hurricane Katrina had ravaged the city and it symbolized that the city was ready to move forward from the death, wreckage and heartache that Katrina’s destruction left behind.

The play was so iconic that it is immortalized in a statue outside the Superdome.

“We are at a similar moment with ALS, similar to the night of the blocked punt, because research is under-funded and under-resourced and patients have no options but to fade away quietly and die, and that is not OK,’’ Gleason said. “With the building of the Team Gleason House, we’re announcing to the world that with right care and right technology patients can be productive for decades. This is an effort that’s bigger than me, bigger than the blocked punt for the city of New Orleans, bigger than football and the Super Bowl.

“This is something that will outlive all of us.’’

mark.cannizzaro@nypost.com

Jumat, 25 Januari 2013

These Pictures Were Drawn (by a person w/ ALS) Using A Human Eyeball. Incredible.

These Pictures Were Drawn (by a person w/ ALS) Using A Human Eyeball. Incredible.


Francis Tsai is a concept artist who has worked for companies like Rockstar, EA and Eidos. Sadly, as we told you last month, Tsai was diagnosed with Lou Gehrig's Disease in 2010, and the condition has slowly taken away his ability to draw.

First he lost the use of his hands, so he learned to draw with his feet; when that was taken away, he promised to learn how to rig up a computer so he could draw with his eyes. Well, Francis' sister emailed us today to let us know these experiments have been a success.

The pictures you're seeing here were drawn by Francis using only his eyeballs. Using Tobii's "eye-gazing" technology, plugged into drawing programs Sketchup and GIMP, Tsai has been able to create these four images using nothing but the motion of his eyeballs. I'm at a loss for words.
You can purchase prints of these from Francis' store, with all proceeds going towards funding his medical care.


To see the larger pics in all their glory (or, if they're big enough, so you can save them as wallpaper), right-click on them below and select "open in new tab".
Fine Art is a celebration of the work of video game artists, showcasing the best of both their professional and personal portfolios. If you're in the business and have some concept, environment, promotional or character art you'd like to share, drop us a line!

These Pictures Were Drawn Using A Human Eyeball. Incredible. These Pictures Were Drawn Using A Human Eyeball. Incredible. These Pictures Were Drawn Using A Human Eyeball. Incredible.

Selasa, 22 Januari 2013

Intel Aims To Give Stephen Hawking’s Speech Device Much Needed Upgrade

Intel Aims To Give Stephen Hawking’s Speech Device Much Needed Upgrade

January 22, 2013


Jedidiah Becker for redOrbit.com – Your Universe Online

For years now, the paralytic conqueror of the cosmos Stephen Hawking has relied on technological gadgetry to serve as the interface between his magnificent mind and the outside world. While a Lou Gehrig-like degenerative disease has slowly eroded his ability to control his own movements for the last five decades, the world-renowned theoretical physicist and pop-science icon has, in a sense, been fortunate. Had he been born a mere twenty years earlier, the brain that first attempted to bridge the cosmological chasm between quantum mechanics and general relativity may have been forever locked away within the confines of a debilitated body.

But as Hawking’s degenerative motor neuron disease has incrementally robbed him of his ability to communicate naturally, the rise of increasingly sophisticated technology has empowered him to continue his work to the benefit of us all. In recent years, however, that technology appears to have plateaued while Professor Hawking’s physical state has all but reached its nadir. With the exception of a few facial muscles that he can still voluntarily twitch, the Cambridge-based cosmologist is now fully paralyzed.

Since the early 2000s, Hawking has relied on an electronic speech-generating device that allows him to use a voluntary cheek twitch to select letters from a screen as a continuously moving cursor as it scrolls through the alphabet. In this manner, letter by letter, word by word, the profoundest thoughts of his lightning-quick mind drip from this cognitive bottleneck at a grueling rate of about one word per minute.

Recently, however, Intel’s chief technology officer Justin Rattner stated he believes that there may be several technologies floating around that could dramatically increase the speed with which Hawking is able to communicate. At last week’s annual Consumer Electronics Show (CES), Rattner noted that an Intel research team could be on the cusp of a new technology that could improve his word count by up to 5 to 10 words per minute.

A renowned computer scientist in his own right, Rattner says that the technology currently used by Hawking utilizes only one of his voluntary motions; namely, the cheek twitch. But as the Intel CES points out, Hawking can also generate small movements in his eyebrow as well as his mouth, and the incorporation of just one of these additional voluntary muscle responses into his communication technology could dramatically increase the speed with which he can communicate. For instance, utilizing two inputs – say cheek plus eyebrow twitch – instead of just one would allow Hawking to use Morse code rather than a lazily scrolling cursor to spell words. And while this might still be slow by almost any other standard, it would still represent a “great improvement” over the current exasperatingly slow one-word-per-minute pace.

Hawking first teamed up with Intel in the late 1990s in the hopes of developing technology that would allow him to overcome his increasingly severe communication impediments. In the past two years, the 71-year-old cosmologist has again actively sought the assistance of the massive multi-national chip maker as his ability to compose text has further diminished.
After an initial meeting with Hawking in early 2012, Rattner says he was unsure whether the current state of the technology was up to snuff for the professor’s expectations. “Up to now, these technologies didn’t work well enough to satisfy someone like Stephen, who wants to produce a lot of information,” he explained.

Currently, Intel is at work on a system that can combine the physicist’s cheek twitch with his mouth and eyebrow movements to generate more complex input signals for his computer. “We’ve built a new, character-driven interface in modern terms that includes a better word predictor,” said Rattner.

THE FUTURE IS INTUITIVE, ENVIRONMENTALLY AWARE TECHNOLOGY

But that’s not the end of the story. Though still in its nascent research and development stage, the world’s largest chip-making company is also tinkering with an entirely new interface that would rely on sophisticated facial recognition software rather than mechanical muscle movements as inputs.
While Hawking is now entirely reliant on Intel’s technology to express himself, the relationship between the brilliant theoretical physicist and the cutting-edge microprocessor firm is by no means one-sided. The very special case of Professor Hawking’s deteriorating motor skills has provided a salient and urgent catalyst for the company’s broader researcher into smart technology and devices for assisting the elderly and disabled. And Hawking’s rigorous and articulate feedback regarding what works, what doesn’t and why has undoubtedly provided Intel’s R&D department with critical insight into how to move forward with these technologies.

According to Rattner, the key to getting smart technology out of the slump that it’s been in for half a decade is to create gadgets that are able to read the user’s environment in an integrated and intuitive manner. Moving forward, Intel’s work in this field will make use of ‘context aware’ devices that combine a variety of environmental inputs using hardware like cameras, microphones and thermometers. The ambient information gleaned from these devices can then be paired with software that tracks the user’s online activity, personal calendars, social media engagement, etc. to create an intimate, predictive and truly ‘smart’ AI assistant. “We use this [information] to reason your current context and what’s important at any given time [and deliver] pervasive assistance,” Rattner explained.

Mark Weiser – the twentieth-century modern computing trailblazer and long-time chief scientist at Xerox Mark – once said that the best technology “should be invisible, get out of your way, and let you live your life.” According to this philosophy, our gadgets should be quiet, invisible servants – a sort of extension of our subconscious. And this is what Intel is currently aiming at with its smart technology research. Rattner hopes to create devices that help not only the physically disabled but eventually all of us by anticipating our needs and desires at the most basic levels. And if Intel has anything to do with it, he says, “we’ll be emotionally connected with our devices in a few years.”


Source: Jedidiah Becker for redOrbit.com – Your Universe Online