Honor eye tracking technology aims to revolutionize smartphone interaction. The company has become the first smartphone brand to introduce intent-based eye tracking technology. This groundbreaking feature, powered by AI, allows users to effortlessly control their phones using only their eyes.
The company has listened to the needs of people with disabilities. International ALS foundations have long advocated for technology that improves the lives of those with limited mobility. By introducing Honor eye tracking technology, the company is making significant strides in accessibility.
This innovative feature will be available globally from August 27th, 2024, through the MagicOS 8.0 operating system. Honor’s commitment to human-centric innovation is evident in this development.
Honor Eye-tracking Technology Makes a Big Leap in Smartphone Accessibility
ALS is a bad disease. It makes muscles weak and stop working. People with ALS often lose the ability to move. But their eyes can still work, and Honor wants to make smartphones more accessible with its eye-tracking technology.
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Limore Noach, executive director of ALS Foundation Netherlands, has shared a little more info about ALS. She says, “Eyes are often the last thing to go.” People with ALS want to do things, even when they’re sick. Honor’s new eye-tracking tech can help. It gives them a way to use their phones again.
The company is working on even cooler tech. Honor is making a special computer that you can control with your brain. This is great news for people who can’t move, like those with ALS. A man named Wei Zhang has tried it. He’s had ALS for a long time. This new tech lets him use a computer just by thinking.
With these efforts, Honor wants to make tech that helps everyone. They’re trying to find new ways for computers and phones to work together. This will make life easier for people with disabilities.
Another thing that’s worth mentioning is that Honor wants people to be aware of ALS. The company has started a #HONORtheChallenger social media challenge. You can participate in it through X, Instagram, TikTok, and Facebook.
Last year, my 68-year-old partner was diagnosed with Lou Gehrig’s disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn’t given him attentive care and attention, as the hospital center didn’t provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using vine health centre . com ALS/MND treatment, which my husband has been receiving for a few months now. I’m delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best.
My husband had ALS/MND programme about 4 months ago. he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. It doesn’t make the ALS go away but it did give him better quality of life. we got the treatment from vine health centre . com
Last year, my 68-year-old partner was diagnosed with Lou Gehrig’s disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn’t given him attentive care and attention, as the hospital center didn’t provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using vine health centre . com ALS/MND treatment, which my husband has been receiving for a few months now. I’m delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best.