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DUKAS_192374272_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair.
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374270_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair Demonstrating how it sits on the brain surface
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374269_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair Demonstrating how ithe device is read using a hand held receiver placed over the area of the brain where it sits
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374268_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair Demonstrating how ithe device is read using a hand held receiver placed over the area of the brain where it sits
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374267_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair Demonstrating how ithe device is read using a hand held receiver placed over the area of the brain where it sits
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374266_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair Demonstrating how ithe device is read using a hand held receiver placed over the area of the brain where it sits
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374265_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair.
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374264_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair Demonstrating how it sits on the brain surface
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374263_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair.
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192374262_FER
Wireless AI-powered brain interface
Ferrari Press Agency
Interface 1
Ref 17436
02/01/2026
See Ferrari text
Pictures MUST credit: Columbia University
A brain implant the size and thickness of a postage stamp is set to improve the quality of life for stroke victims and other brain conditions — by emailing thoughts to AI using wi-fi.
The new silicon brain computer interface also aims to expand treatment possibilities for neurological conditions such as epilepsy, spinal cord injury, the degenerative disease ALS and blindness.
The team behind it says the implant – will help manage seizures and restore motor, speech, and visual function.
This is done by providing a minimally invasive, high-throughput information link directly to and from the brain.
The transformational potential of this new system lies in its small size and ability to transfer data at high rates.
It has been developed by US researchers at Columbia University, NewYork-Presbyterian, Stanford University, and the University of Pennsylvania.
The interface relies on a single silicon chip to establish a wireless, high-bandwidth connection between the brain and any external computer.
The platform is called the Biological Interface System to Cortex or BISC for short.
OPS: The new device called the Biological Interface System to Cortex (BISC).As thin as a human hair.
Pictrure supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345190_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345189_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345188_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345187_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345186_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345185_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345184_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345183_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192345182_FER
AI headset for guiding the blind
Ferrari Press Agency
Blind 1
Ref 17434
31/12/2025
See Ferrari pictures
Pictures MUST credit: .lumen
Self-driving technology for cars has been turned into a walking aid for the blind.
The .lumen Glasses help people with various sight conditions to navigate the world without using a guide dog or white stick.
They take self-driving technology and scale it down to something that can be worn on the head.
The AI-powered wearable enables blind people to move independently, without internet connectivity, pre-mapped environments or constant audio instructions.
The premise behind the Romanian design device is that vision is not the same as perception.
Autonomous systems don’t need to be able to see the world the way humans do.
They need to understand space: what is near, what is moving, what is safe, what is not.
Instead of screens or commands, the .lumen Glasses use a patented haptic interface that gently guides head movement with vibrations offering intuitive direction in real time.
OPS: The .lumen Glasses headset uses AI , cameras and obstacle detectiing LIDAR to guide users .
Picture supplied by Ferrari (FOTO: DUKAS/FERRARI PRESS) -
DUKAS_192239476_ZUM
Calcutta Blind School Christmas Party
December 22, 2025, Kolkata, West Bengal, India: Visually disabled students participate Christmas celebrations at a Calcutta blind school organised by B.B.Poddor eye hospital in Kolkata. Christmas is popular in the primarily Hindu country and is celebrated widely across the nation. (Credit Image: © Rupak De Chowdhuri/ZUMA Press Wire (FOTO: DUKAS/ZUMA)
Represented by ZUMA Press, Inc. -
DUKAS_190270368_NUR
Graduates With Disabilities Protest For Jobs In Dhaka
A group of unemployed graduates with disabilities protests, demanding urgent government measures to ensure employment opportunities for persons with disabilities in Dhaka, Bangladesh, on October 22, 2025. They urge five key reforms to ensure fair employment for persons with disabilities: special recruitment every two years, a 2% quota in higher and 5% in lower government jobs, revision of the scribe policy to allow own scribes, reserved posts for visually impaired candidates in disability education centers, and raising the government job age limit to 35 years (or 37 if the general limit increases). (Photo by Zakir Hossain Chowdhury/NurPhoto) -
DUKAS_190270367_NUR
Graduates With Disabilities Protest For Jobs In Dhaka
A group of unemployed graduates with disabilities protests, demanding urgent government measures to ensure employment opportunities for persons with disabilities in Dhaka, Bangladesh, on October 22, 2025. They urge five key reforms to ensure fair employment for persons with disabilities: special recruitment every two years, a 2% quota in higher and 5% in lower government jobs, revision of the scribe policy to allow own scribes, reserved posts for visually impaired candidates in disability education centers, and raising the government job age limit to 35 years (or 37 if the general limit increases). (Photo by Zakir Hossain Chowdhury/NurPhoto) -
DUKAS_190270366_NUR
Graduates With Disabilities Protest For Jobs In Dhaka
A group of unemployed graduates with disabilities protests, demanding urgent government measures to ensure employment opportunities for persons with disabilities in Dhaka, Bangladesh, on October 22, 2025. They urge five key reforms to ensure fair employment for persons with disabilities: special recruitment every two years, a 2% quota in higher and 5% in lower government jobs, revision of the scribe policy to allow own scribes, reserved posts for visually impaired candidates in disability education centers, and raising the government job age limit to 35 years (or 37 if the general limit increases). (Photo by Zakir Hossain Chowdhury/NurPhoto) -
DUKAS_190270364_NUR
Graduates With Disabilities Protest For Jobs In Dhaka
A group of unemployed graduates with disabilities protests, demanding urgent government measures to ensure employment opportunities for persons with disabilities in Dhaka, Bangladesh, on October 22, 2025. They urge five key reforms to ensure fair employment for persons with disabilities: special recruitment every two years, a 2% quota in higher and 5% in lower government jobs, revision of the scribe policy to allow own scribes, reserved posts for visually impaired candidates in disability education centers, and raising the government job age limit to 35 years (or 37 if the general limit increases). (Photo by Zakir Hossain Chowdhury/NurPhoto) -
DUKAS_190270363_NUR
Graduates With Disabilities Protest For Jobs In Dhaka
A group of unemployed graduates with disabilities protests, demanding urgent government measures to ensure employment opportunities for persons with disabilities in Dhaka, Bangladesh, on October 22, 2025. They urge five key reforms to ensure fair employment for persons with disabilities: special recruitment every two years, a 2% quota in higher and 5% in lower government jobs, revision of the scribe policy to allow own scribes, reserved posts for visually impaired candidates in disability education centers, and raising the government job age limit to 35 years (or 37 if the general limit increases). (Photo by Zakir Hossain Chowdhury/NurPhoto) -
DUKAS_190270347_NUR
Graduates With Disabilities Protest For Jobs In Dhaka
A group of unemployed graduates with disabilities protests, demanding urgent government measures to ensure employment opportunities for persons with disabilities in Dhaka, Bangladesh, on October 22, 2025. They urge five key reforms to ensure fair employment for persons with disabilities: special recruitment every two years, a 2% quota in higher and 5% in lower government jobs, revision of the scribe policy to allow own scribes, reserved posts for visually impaired candidates in disability education centers, and raising the government job age limit to 35 years (or 37 if the general limit increases). (Photo by Zakir Hossain Chowdhury/NurPhoto) -
DUKAS_187269746_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269742_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269738_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269734_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269731_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269728_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269725_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269722_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269719_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269716_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269713_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_187269708_FER
Remore controlled squirel helps train guide dogs
Ferrari Press Agency
Squirrel 1
Ref 17026
25/07/2025
See Ferrari text
Picture MUST credit: Guide Dogs
A guide dog training variety has new aid for preparing its pups for the outside world — remote controlled squirrels.
The new canine training device is a stuffed toy squirrel strapped to a remotely operated model car.
When a dog and its handler are out walking, a member of staff activates the squirrel and zooms it across the mutt’s path.
The dog is then training to ignore the distraction and carry ointment its route.
The move is designed to help future guide dogs resist one of the canine world’s most chaotic distractions.
A poll for UK organisation Guide Dogs which commissioned the bot, showed that 35% of everyday pups chase squirrels and 60% of dog owners admitting their pet could never hack it as a guide dog.
Guide Dogs training and behaviour expert Karen Brady said the aim is get dogs so used to chaos that it becomes background noise.
She explained that one moment of lost focus could endanger both the dog and its user.
OPS: A guide dog in training in London being taught to ignore the remote controlled squirrel.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUK10163096_002
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_013
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_011
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_003
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_001
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_010
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_008
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_007
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_006
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_009
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_004
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_012
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
