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DUK10163225_007
Happy Birthday: Wombat Bucky feiert im Australian Reptile Park seinen ersten Geburtstag
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
An orphaned wombat has just celebrated his very first birthday.
Bucky, who lives at the Australian Reptile Park, was rescued last year after his mother was tragically struck by a car. Found at the side of the road, he’s since been cared for lovingly by the park's team.
To celebrate the special occasion, Bucky’s dedicated surrogate mum and mammals keeper, Ellesha Vaness, created a handmade birthday bouquet packed with his favourites – fresh grass, sweet potato, and carrot. True to his playful nature, Bucky devoured the treat with delight before dashing off to cheekily chase Ellesha around.
“Watching Bucky thrive over the past year has been such a joy,” said Ellesha Vaness. “When I first met him, he was so tiny and vulnerable. Now he’s full of personality and cheekiness.”
Beyond Bucky’s adorable milestone, his journey highlights a pressing issue: wombat conservation. Across Australia, wombats face growing threats from habitat loss, disease, and particularly road accidents, with vehicle collisions remaining a leading danger.
“Bucky’s story is a reminder of how fragile our native wildlife populations can be,” said Vaness. “We urge everyone to slow down on the roads, especially in wildlife-prone areas. One moment of caution could save a life like Bucky’s.”
Visitors to the Australian Reptile Park can meet Bucky in person through wombat encounters, learning more about wombat conservation efforts and witnessing firsthand the remarkable bond he shares with his devoted keepers.
Featuring: Bucky
When: 28 Apr 2025
Credit: Australian Reptile Park/Cover Images
*** Local Caption *** 47368641
(c) Dukas -
DUK10163225_001
Happy Birthday: Wombat Bucky feiert im Australian Reptile Park seinen ersten Geburtstag
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
An orphaned wombat has just celebrated his very first birthday.
Bucky, who lives at the Australian Reptile Park, was rescued last year after his mother was tragically struck by a car. Found at the side of the road, he’s since been cared for lovingly by the park's team.
To celebrate the special occasion, Bucky’s dedicated surrogate mum and mammals keeper, Ellesha Vaness, created a handmade birthday bouquet packed with his favourites – fresh grass, sweet potato, and carrot. True to his playful nature, Bucky devoured the treat with delight before dashing off to cheekily chase Ellesha around.
“Watching Bucky thrive over the past year has been such a joy,” said Ellesha Vaness. “When I first met him, he was so tiny and vulnerable. Now he’s full of personality and cheekiness.”
Beyond Bucky’s adorable milestone, his journey highlights a pressing issue: wombat conservation. Across Australia, wombats face growing threats from habitat loss, disease, and particularly road accidents, with vehicle collisions remaining a leading danger.
“Bucky’s story is a reminder of how fragile our native wildlife populations can be,” said Vaness. “We urge everyone to slow down on the roads, especially in wildlife-prone areas. One moment of caution could save a life like Bucky’s.”
Visitors to the Australian Reptile Park can meet Bucky in person through wombat encounters, learning more about wombat conservation efforts and witnessing firsthand the remarkable bond he shares with his devoted keepers.
Featuring: Bucky
When: 28 Apr 2025
Credit: Australian Reptile Park/Cover Images
*** Local Caption *** 47368643
(c) Dukas -
DUK10163225_006
Happy Birthday: Wombat Bucky feiert im Australian Reptile Park seinen ersten Geburtstag
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
An orphaned wombat has just celebrated his very first birthday.
Bucky, who lives at the Australian Reptile Park, was rescued last year after his mother was tragically struck by a car. Found at the side of the road, he’s since been cared for lovingly by the park's team.
To celebrate the special occasion, Bucky’s dedicated surrogate mum and mammals keeper, Ellesha Vaness, created a handmade birthday bouquet packed with his favourites – fresh grass, sweet potato, and carrot. True to his playful nature, Bucky devoured the treat with delight before dashing off to cheekily chase Ellesha around.
“Watching Bucky thrive over the past year has been such a joy,” said Ellesha Vaness. “When I first met him, he was so tiny and vulnerable. Now he’s full of personality and cheekiness.”
Beyond Bucky’s adorable milestone, his journey highlights a pressing issue: wombat conservation. Across Australia, wombats face growing threats from habitat loss, disease, and particularly road accidents, with vehicle collisions remaining a leading danger.
“Bucky’s story is a reminder of how fragile our native wildlife populations can be,” said Vaness. “We urge everyone to slow down on the roads, especially in wildlife-prone areas. One moment of caution could save a life like Bucky’s.”
Visitors to the Australian Reptile Park can meet Bucky in person through wombat encounters, learning more about wombat conservation efforts and witnessing firsthand the remarkable bond he shares with his devoted keepers.
Featuring: Bucky
When: 28 Apr 2025
Credit: Australian Reptile Park/Cover Images
*** Local Caption *** 47368642
(c) Dukas -
DUK10163225_005
Happy Birthday: Wombat Bucky feiert im Australian Reptile Park seinen ersten Geburtstag
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
An orphaned wombat has just celebrated his very first birthday.
Bucky, who lives at the Australian Reptile Park, was rescued last year after his mother was tragically struck by a car. Found at the side of the road, he’s since been cared for lovingly by the park's team.
To celebrate the special occasion, Bucky’s dedicated surrogate mum and mammals keeper, Ellesha Vaness, created a handmade birthday bouquet packed with his favourites – fresh grass, sweet potato, and carrot. True to his playful nature, Bucky devoured the treat with delight before dashing off to cheekily chase Ellesha around.
“Watching Bucky thrive over the past year has been such a joy,” said Ellesha Vaness. “When I first met him, he was so tiny and vulnerable. Now he’s full of personality and cheekiness.”
Beyond Bucky’s adorable milestone, his journey highlights a pressing issue: wombat conservation. Across Australia, wombats face growing threats from habitat loss, disease, and particularly road accidents, with vehicle collisions remaining a leading danger.
“Bucky’s story is a reminder of how fragile our native wildlife populations can be,” said Vaness. “We urge everyone to slow down on the roads, especially in wildlife-prone areas. One moment of caution could save a life like Bucky’s.”
Visitors to the Australian Reptile Park can meet Bucky in person through wombat encounters, learning more about wombat conservation efforts and witnessing firsthand the remarkable bond he shares with his devoted keepers.
Featuring: Bucky, Ellesha Vaness
When: 28 Apr 2025
Credit: Australian Reptile Park/Cover Images
*** Local Caption *** 47368644
(c) Dukas -
DUK10163225_004
Happy Birthday: Wombat Bucky feiert im Australian Reptile Park seinen ersten Geburtstag
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
An orphaned wombat has just celebrated his very first birthday.
Bucky, who lives at the Australian Reptile Park, was rescued last year after his mother was tragically struck by a car. Found at the side of the road, he’s since been cared for lovingly by the park's team.
To celebrate the special occasion, Bucky’s dedicated surrogate mum and mammals keeper, Ellesha Vaness, created a handmade birthday bouquet packed with his favourites – fresh grass, sweet potato, and carrot. True to his playful nature, Bucky devoured the treat with delight before dashing off to cheekily chase Ellesha around.
“Watching Bucky thrive over the past year has been such a joy,” said Ellesha Vaness. “When I first met him, he was so tiny and vulnerable. Now he’s full of personality and cheekiness.”
Beyond Bucky’s adorable milestone, his journey highlights a pressing issue: wombat conservation. Across Australia, wombats face growing threats from habitat loss, disease, and particularly road accidents, with vehicle collisions remaining a leading danger.
“Bucky’s story is a reminder of how fragile our native wildlife populations can be,” said Vaness. “We urge everyone to slow down on the roads, especially in wildlife-prone areas. One moment of caution could save a life like Bucky’s.”
Visitors to the Australian Reptile Park can meet Bucky in person through wombat encounters, learning more about wombat conservation efforts and witnessing firsthand the remarkable bond he shares with his devoted keepers.
Featuring: Bucky
When: 28 Apr 2025
Credit: Australian Reptile Park/Cover Images
*** Local Caption *** 47368638
(c) Dukas -
DUK10163225_002
Happy Birthday: Wombat Bucky feiert im Australian Reptile Park seinen ersten Geburtstag
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
An orphaned wombat has just celebrated his very first birthday.
Bucky, who lives at the Australian Reptile Park, was rescued last year after his mother was tragically struck by a car. Found at the side of the road, he’s since been cared for lovingly by the park's team.
To celebrate the special occasion, Bucky’s dedicated surrogate mum and mammals keeper, Ellesha Vaness, created a handmade birthday bouquet packed with his favourites – fresh grass, sweet potato, and carrot. True to his playful nature, Bucky devoured the treat with delight before dashing off to cheekily chase Ellesha around.
“Watching Bucky thrive over the past year has been such a joy,” said Ellesha Vaness. “When I first met him, he was so tiny and vulnerable. Now he’s full of personality and cheekiness.”
Beyond Bucky’s adorable milestone, his journey highlights a pressing issue: wombat conservation. Across Australia, wombats face growing threats from habitat loss, disease, and particularly road accidents, with vehicle collisions remaining a leading danger.
“Bucky’s story is a reminder of how fragile our native wildlife populations can be,” said Vaness. “We urge everyone to slow down on the roads, especially in wildlife-prone areas. One moment of caution could save a life like Bucky’s.”
Visitors to the Australian Reptile Park can meet Bucky in person through wombat encounters, learning more about wombat conservation efforts and witnessing firsthand the remarkable bond he shares with his devoted keepers.
Featuring: Bucky
When: 28 Apr 2025
Credit: Australian Reptile Park/Cover Images
*** Local Caption *** 47368640
(c) Dukas -
DUK10163225_003
Happy Birthday: Wombat Bucky feiert im Australian Reptile Park seinen ersten Geburtstag
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
An orphaned wombat has just celebrated his very first birthday.
Bucky, who lives at the Australian Reptile Park, was rescued last year after his mother was tragically struck by a car. Found at the side of the road, he’s since been cared for lovingly by the park's team.
To celebrate the special occasion, Bucky’s dedicated surrogate mum and mammals keeper, Ellesha Vaness, created a handmade birthday bouquet packed with his favourites – fresh grass, sweet potato, and carrot. True to his playful nature, Bucky devoured the treat with delight before dashing off to cheekily chase Ellesha around.
“Watching Bucky thrive over the past year has been such a joy,” said Ellesha Vaness. “When I first met him, he was so tiny and vulnerable. Now he’s full of personality and cheekiness.”
Beyond Bucky’s adorable milestone, his journey highlights a pressing issue: wombat conservation. Across Australia, wombats face growing threats from habitat loss, disease, and particularly road accidents, with vehicle collisions remaining a leading danger.
“Bucky’s story is a reminder of how fragile our native wildlife populations can be,” said Vaness. “We urge everyone to slow down on the roads, especially in wildlife-prone areas. One moment of caution could save a life like Bucky’s.”
Visitors to the Australian Reptile Park can meet Bucky in person through wombat encounters, learning more about wombat conservation efforts and witnessing firsthand the remarkable bond he shares with his devoted keepers.
Featuring: Bucky, Ellesha Vaness
When: 28 Apr 2025
Credit: Australian Reptile Park/Cover Images
*** Local Caption *** 47368639
(c) Dukas -
DUK10163226_007
Herzerkrankung von den Doktoren übersehen: Dan Cipriani konnte dank seiner neuen Smartwatch selbst eine supraventrikuläre Tachykardie diagnostizieren
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Sarah Ingram
The symptoms were scary. Dan Cipriani’s heart rate would speed up and he would feel lightheaded and dizzy - sometimes while exercising and at others while he was at rest.
Dan first went to the doctor when he was 13 with sudden random onset palpitations, but he left the GP’s office without answers.
Dan went back another five times over the years and always left with doctors scratching their heads.
He was given a battery of tests; wearing a heart monitor for days on end or booking into hospital for echocardiograms and ECGs - but nothing was conclusive.
Meanwhile, the episodes kept happening. Dan’s heart rate would reach 220 BPM while sitting down; when it should have been between 60 and 100.
The 32-year-old banking director from London has always been fitness-mad.
He has run countless sub-three hour marathons, three ultra marathons including one 100-mile race and has competed in an Ironman.
He could not be healthier, but each time he would exercise, he would experience these troubling episodes.
‘They happened probably once a fortnight but then became more frequent over the last two years and would last longer, perhaps up to a minute,’ he says.
‘They also always happened during intense exercise. I did an Ironman triathlon and the London Marathon, and my heart rate jumped up to 220 beats a minute during the races, which was scary. I’ve had different diagnoses from stress with my work to potentially low blood sugar’, he explains.
Then, a year ago, he was finally given a diagnosis. After an event where his heart raced constantly at 220BPM, he decided he’d had enough and went back to his cardiologist and demanded answers.
‘My doctor told me to buy a Kardia monitor, which is an ECG device you attach to your phone so you can track a cardiac event when it happens. The day after I bought it, I had an episode and caught it with the monitor, sent it to my cardiologist, and he knew immediately what it w *** Lo
(c) Dukas -
DUK10163226_004
Herzerkrankung von den Doktoren übersehen: Dan Cipriani konnte dank seiner neuen Smartwatch selbst eine supraventrikuläre Tachykardie diagnostizieren
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Sarah Ingram
The symptoms were scary. Dan Cipriani’s heart rate would speed up and he would feel lightheaded and dizzy - sometimes while exercising and at others while he was at rest.
Dan first went to the doctor when he was 13 with sudden random onset palpitations, but he left the GP’s office without answers.
Dan went back another five times over the years and always left with doctors scratching their heads.
He was given a battery of tests; wearing a heart monitor for days on end or booking into hospital for echocardiograms and ECGs - but nothing was conclusive.
Meanwhile, the episodes kept happening. Dan’s heart rate would reach 220 BPM while sitting down; when it should have been between 60 and 100.
The 32-year-old banking director from London has always been fitness-mad.
He has run countless sub-three hour marathons, three ultra marathons including one 100-mile race and has competed in an Ironman.
He could not be healthier, but each time he would exercise, he would experience these troubling episodes.
‘They happened probably once a fortnight but then became more frequent over the last two years and would last longer, perhaps up to a minute,’ he says.
‘They also always happened during intense exercise. I did an Ironman triathlon and the London Marathon, and my heart rate jumped up to 220 beats a minute during the races, which was scary. I’ve had different diagnoses from stress with my work to potentially low blood sugar’, he explains.
Then, a year ago, he was finally given a diagnosis. After an event where his heart raced constantly at 220BPM, he decided he’d had enough and went back to his cardiologist and demanded answers.
‘My doctor told me to buy a Kardia monitor, which is an ECG device you attach to your phone so you can track a cardiac event when it happens. The day after I bought it, I had an episode and caught it with the monitor, sent it to my cardiologist, and he knew immediately what it w *** Lo
(c) Dukas -
DUK10163226_006
Herzerkrankung von den Doktoren übersehen: Dan Cipriani konnte dank seiner neuen Smartwatch selbst eine supraventrikuläre Tachykardie diagnostizieren
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Sarah Ingram
The symptoms were scary. Dan Cipriani’s heart rate would speed up and he would feel lightheaded and dizzy - sometimes while exercising and at others while he was at rest.
Dan first went to the doctor when he was 13 with sudden random onset palpitations, but he left the GP’s office without answers.
Dan went back another five times over the years and always left with doctors scratching their heads.
He was given a battery of tests; wearing a heart monitor for days on end or booking into hospital for echocardiograms and ECGs - but nothing was conclusive.
Meanwhile, the episodes kept happening. Dan’s heart rate would reach 220 BPM while sitting down; when it should have been between 60 and 100.
The 32-year-old banking director from London has always been fitness-mad.
He has run countless sub-three hour marathons, three ultra marathons including one 100-mile race and has competed in an Ironman.
He could not be healthier, but each time he would exercise, he would experience these troubling episodes.
‘They happened probably once a fortnight but then became more frequent over the last two years and would last longer, perhaps up to a minute,’ he says.
‘They also always happened during intense exercise. I did an Ironman triathlon and the London Marathon, and my heart rate jumped up to 220 beats a minute during the races, which was scary. I’ve had different diagnoses from stress with my work to potentially low blood sugar’, he explains.
Then, a year ago, he was finally given a diagnosis. After an event where his heart raced constantly at 220BPM, he decided he’d had enough and went back to his cardiologist and demanded answers.
‘My doctor told me to buy a Kardia monitor, which is an ECG device you attach to your phone so you can track a cardiac event when it happens. The day after I bought it, I had an episode and caught it with the monitor, sent it to my cardiologist, and he knew immediately what it w *** Lo
(c) Dukas -
DUK10163226_003
Herzerkrankung von den Doktoren übersehen: Dan Cipriani konnte dank seiner neuen Smartwatch selbst eine supraventrikuläre Tachykardie diagnostizieren
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Sarah Ingram
The symptoms were scary. Dan Cipriani’s heart rate would speed up and he would feel lightheaded and dizzy - sometimes while exercising and at others while he was at rest.
Dan first went to the doctor when he was 13 with sudden random onset palpitations, but he left the GP’s office without answers.
Dan went back another five times over the years and always left with doctors scratching their heads.
He was given a battery of tests; wearing a heart monitor for days on end or booking into hospital for echocardiograms and ECGs - but nothing was conclusive.
Meanwhile, the episodes kept happening. Dan’s heart rate would reach 220 BPM while sitting down; when it should have been between 60 and 100.
The 32-year-old banking director from London has always been fitness-mad.
He has run countless sub-three hour marathons, three ultra marathons including one 100-mile race and has competed in an Ironman.
He could not be healthier, but each time he would exercise, he would experience these troubling episodes.
‘They happened probably once a fortnight but then became more frequent over the last two years and would last longer, perhaps up to a minute,’ he says.
‘They also always happened during intense exercise. I did an Ironman triathlon and the London Marathon, and my heart rate jumped up to 220 beats a minute during the races, which was scary. I’ve had different diagnoses from stress with my work to potentially low blood sugar’, he explains.
Then, a year ago, he was finally given a diagnosis. After an event where his heart raced constantly at 220BPM, he decided he’d had enough and went back to his cardiologist and demanded answers.
‘My doctor told me to buy a Kardia monitor, which is an ECG device you attach to your phone so you can track a cardiac event when it happens. The day after I bought it, I had an episode and caught it with the monitor, sent it to my cardiologist, and he knew immediately what it w *** Lo
(c) Dukas -
DUK10163226_002
Herzerkrankung von den Doktoren übersehen: Dan Cipriani konnte dank seiner neuen Smartwatch selbst eine supraventrikuläre Tachykardie diagnostizieren
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Sarah Ingram
The symptoms were scary. Dan Cipriani’s heart rate would speed up and he would feel lightheaded and dizzy - sometimes while exercising and at others while he was at rest.
Dan first went to the doctor when he was 13 with sudden random onset palpitations, but he left the GP’s office without answers.
Dan went back another five times over the years and always left with doctors scratching their heads.
He was given a battery of tests; wearing a heart monitor for days on end or booking into hospital for echocardiograms and ECGs - but nothing was conclusive.
Meanwhile, the episodes kept happening. Dan’s heart rate would reach 220 BPM while sitting down; when it should have been between 60 and 100.
The 32-year-old banking director from London has always been fitness-mad.
He has run countless sub-three hour marathons, three ultra marathons including one 100-mile race and has competed in an Ironman.
He could not be healthier, but each time he would exercise, he would experience these troubling episodes.
‘They happened probably once a fortnight but then became more frequent over the last two years and would last longer, perhaps up to a minute,’ he says.
‘They also always happened during intense exercise. I did an Ironman triathlon and the London Marathon, and my heart rate jumped up to 220 beats a minute during the races, which was scary. I’ve had different diagnoses from stress with my work to potentially low blood sugar’, he explains.
Then, a year ago, he was finally given a diagnosis. After an event where his heart raced constantly at 220BPM, he decided he’d had enough and went back to his cardiologist and demanded answers.
‘My doctor told me to buy a Kardia monitor, which is an ECG device you attach to your phone so you can track a cardiac event when it happens. The day after I bought it, I had an episode and caught it with the monitor, sent it to my cardiologist, and he knew immediately what it w *** Lo
(c) Dukas -
DUK10163226_001
Herzerkrankung von den Doktoren übersehen: Dan Cipriani konnte dank seiner neuen Smartwatch selbst eine supraventrikuläre Tachykardie diagnostizieren
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Sarah Ingram
The symptoms were scary. Dan Cipriani’s heart rate would speed up and he would feel lightheaded and dizzy - sometimes while exercising and at others while he was at rest.
Dan first went to the doctor when he was 13 with sudden random onset palpitations, but he left the GP’s office without answers.
Dan went back another five times over the years and always left with doctors scratching their heads.
He was given a battery of tests; wearing a heart monitor for days on end or booking into hospital for echocardiograms and ECGs - but nothing was conclusive.
Meanwhile, the episodes kept happening. Dan’s heart rate would reach 220 BPM while sitting down; when it should have been between 60 and 100.
The 32-year-old banking director from London has always been fitness-mad.
He has run countless sub-three hour marathons, three ultra marathons including one 100-mile race and has competed in an Ironman.
He could not be healthier, but each time he would exercise, he would experience these troubling episodes.
‘They happened probably once a fortnight but then became more frequent over the last two years and would last longer, perhaps up to a minute,’ he says.
‘They also always happened during intense exercise. I did an Ironman triathlon and the London Marathon, and my heart rate jumped up to 220 beats a minute during the races, which was scary. I’ve had different diagnoses from stress with my work to potentially low blood sugar’, he explains.
Then, a year ago, he was finally given a diagnosis. After an event where his heart raced constantly at 220BPM, he decided he’d had enough and went back to his cardiologist and demanded answers.
‘My doctor told me to buy a Kardia monitor, which is an ECG device you attach to your phone so you can track a cardiac event when it happens. The day after I bought it, I had an episode and caught it with the monitor, sent it to my cardiologist, and he knew immediately what it w *** Lo
(c) Dukas -
DUK10163226_005
Herzerkrankung von den Doktoren übersehen: Dan Cipriani konnte dank seiner neuen Smartwatch selbst eine supraventrikuläre Tachykardie diagnostizieren
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Sarah Ingram
The symptoms were scary. Dan Cipriani’s heart rate would speed up and he would feel lightheaded and dizzy - sometimes while exercising and at others while he was at rest.
Dan first went to the doctor when he was 13 with sudden random onset palpitations, but he left the GP’s office without answers.
Dan went back another five times over the years and always left with doctors scratching their heads.
He was given a battery of tests; wearing a heart monitor for days on end or booking into hospital for echocardiograms and ECGs - but nothing was conclusive.
Meanwhile, the episodes kept happening. Dan’s heart rate would reach 220 BPM while sitting down; when it should have been between 60 and 100.
The 32-year-old banking director from London has always been fitness-mad.
He has run countless sub-three hour marathons, three ultra marathons including one 100-mile race and has competed in an Ironman.
He could not be healthier, but each time he would exercise, he would experience these troubling episodes.
‘They happened probably once a fortnight but then became more frequent over the last two years and would last longer, perhaps up to a minute,’ he says.
‘They also always happened during intense exercise. I did an Ironman triathlon and the London Marathon, and my heart rate jumped up to 220 beats a minute during the races, which was scary. I’ve had different diagnoses from stress with my work to potentially low blood sugar’, he explains.
Then, a year ago, he was finally given a diagnosis. After an event where his heart raced constantly at 220BPM, he decided he’d had enough and went back to his cardiologist and demanded answers.
‘My doctor told me to buy a Kardia monitor, which is an ECG device you attach to your phone so you can track a cardiac event when it happens. The day after I bought it, I had an episode and caught it with the monitor, sent it to my cardiologist, and he knew immediately what it w *** Lo
(c) Dukas -
DUK10163163_002
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_004
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_005
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_007
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_006
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_009
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_003
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_001
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163163_008
Bekommt ihre eigene Madame Tussauds Wachsfigur: 'The Last Of Us' Star Bella Ramsey wird in London exakt vermessen
SONDERKONDITIONEN: Satzpreis!
**VIDEO AVAILABLE. CONTACT INFO@COVERMG.COM TO RECEIVE.**
Madame Tussauds London has announced Bella Ramsey will soon be joining its famous waxwork family — with a brand-new figure launching later this year.
The news comes as Ramsey rides high on the wave of success, with the second season of HBO’s The Last of Us — where they star as Ellie Williams opposite Pedro Pascal’s Joel Miller — currently in the spotlight.
Ramsey, who burst onto the scene at just 11 years old as the fearless Lyanna Mormont in Game of Thrones, has worked closely with the museum’s expert team since last year. So far, the collaborative process has involved detailed sittings for measurements and reference shots, as well as selecting a signature outfit for the figure and reviewing the initial sculpt.
And the chosen look is none other than the bold Undercover ensemble Ramsey wore at The Last of Us LA premiere — a striking statement donated by the Japanese streetwear label itself.
“It’s an honour to work with Madame Tussauds London’s world-class artists on my first-ever figure,” said Bella. “I am in awe at the level of detail that the artists put into their work, and it has been such a fun experience to be included in their creative process. I can’t wait to see the finished look and to share it with fans.”
Madame Tussauds has shared exclusive footage from inside its studio, showing artists capturing every intricate detail of the actor’s likeness.
Steve Blackburn, General Manager at Madame Tussauds London, added: “Bella Ramsey is a film, TV, and style icon! They shine as brightly on screen as they do in-person, never compromising who they are or what they stand for. And working with them to ensure their first-ever Madame Tussauds figure is an exact likeness has been a delight. We hope fans love the outfit choice too – the standout Undercover look from the recent *The Last of Us* LA premiere, chosen by Bella and kindly donated by the Jap *** Local Caption *** 473
(c) Dukas -
DUK10163164_009
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322461
(c) Dukas -
DUK10163164_005
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322472
(c) Dukas -
DUK10163164_007
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322459
(c) Dukas -
DUK10163164_010
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322452
(c) Dukas -
DUK10163164_003
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322451
(c) Dukas -
DUK10163164_011
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322469
(c) Dukas -
DUK10163164_006
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322466
(c) Dukas -
DUK10163164_004
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322456
(c) Dukas -
DUK10163164_002
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322450
(c) Dukas -
DUK10163164_008
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322447
(c) Dukas -
DUK10163164_012
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322460
(c) Dukas -
DUK10163164_001
Inklusive funktionsfähigem Flammenwerfer: Mecum Auctions, Inc. in Walworth, Wisconsin versteigert eine Batmobile Replik aus dem 1989er Film von Tim Burton
SONDERKONDITIONEN: Satzpreis!
A jaw-dropping replica of the iconic Batmobile from Tim Burton’s 1989 Batman is going under the hammer — but it’ll cost you a hefty £200,000.
Measuring nearly 20 feet long, the supercar was built for the Batman stunt show and comes officially licensed by Warner Bros.
The beast of a machine was constructed by Hollywood Productions and rides on a lengthened Chevrolet Impala chassis.
Signed by original Batmobile builders Chris Dixon and Steve Mank of Wounded Knee Motors in Ohio, it’s the real deal, complete with a Certificate of Ownership from Six Flags.
The glossy black fiberglass body closely mirrors the cinematic original and conceals a Chevrolet 350 CI small-block V8 engine paired with automatic transmission.
Inside, the Batmobile boasts a cockpit-style cabin with a sliding canopy, custom leather seats, and a dazzling array of buttons, switches, and levers.
The interior is decked out with a custom Batman logo on the steering wheel and a Wounded Knee Motors badge just behind the driver’s seat.
Adding to its flair, the vehicle features a British Harrier jet intake and a rear flame thrower for an afterburner-like effect.
Though technically driveable, parking this 20-foot hero-mobile might require Batcave-level planning.
The one-of-a-kind machine — dubbed Serial No. 1 — will be auctioned by American auction company Mecum Auctions on Saturday, May 17.
When: 22 Apr 2025
Credit: Mecum Auctions, Inc./Cover Images
*** Local Caption *** 47322448
(c) Dukas -
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 -
DUK10163096_005
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 -
DUK10163068_001
Besseres Liebesleben durch Diäterfolg - Christina Angela Dains und Nathan Arreola aus Bakersfield haben zusammen 34 Kilo abgenommen und finden sich jetzt wieder attraktiv
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
As a couple, they spent their time together enjoying takeaway meals, drinking alcohol, lazing on the couch watching television - and asking themselves why they were putting on weight.
Nathan Arreola, 28, and Christina Angela Dains, 30, were both struggling with health issues such as reflux, pre-diabetes and depression — but hadn’t made the connection that their weight was affecting their health and wellbeing.
“Most of our time spent together consisted of take-out meals, alcohol consumption, and being inactive,” Nathan remembers.
“We spent a lot of time complaining and asking ourselves why we were putting on so much bad weight, while stuffing our faces on the couch watching television.
“We would often try and cook healthier meals, to the best of our knowledge then, but it would usually spoil and go to waste because we couldn’t fight off the craving, leaving us to eating out or ordering in from the local pizza shop.
“My lifestyle was a far cry from anything resembling healthy. As a kid, I’d always been the skinny, scrawny one in the crowd—lanky and light. But as I transitioned into adulthood, that changed.
“Laziness crept in, and I stopped paying attention to what I was putting into my body—food and alcohol became thoughtless habits. The heaviest I ever got was 210 pounds (95 kilos), a number that still jolts me when I think about it.
“Growing up, I hovered around 150 pounds (68 kilos), so ballooning to over a third more than my norm was a shocking departure. I’d flip through old photos from my early twenties, struck by how slim I once was, almost missing that version of myself.
“Clothes told the story too—I went from slipping comfortably into medium shirts to squeezing into them, eventually surrendering to a wardrobe of larger sizes that felt foreign.
“At the peak of this unhealthy shift, I’d layer up in oversized sweatshirts even in the sweltering 90-degree summers, not *** Local Caption *** 47
(c) Dukas -
DUK10163068_004
Besseres Liebesleben durch Diäterfolg - Christina Angela Dains und Nathan Arreola aus Bakersfield haben zusammen 34 Kilo abgenommen und finden sich jetzt wieder attraktiv
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
As a couple, they spent their time together enjoying takeaway meals, drinking alcohol, lazing on the couch watching television - and asking themselves why they were putting on weight.
Nathan Arreola, 28, and Christina Angela Dains, 30, were both struggling with health issues such as reflux, pre-diabetes and depression — but hadn’t made the connection that their weight was affecting their health and wellbeing.
“Most of our time spent together consisted of take-out meals, alcohol consumption, and being inactive,” Nathan remembers.
“We spent a lot of time complaining and asking ourselves why we were putting on so much bad weight, while stuffing our faces on the couch watching television.
“We would often try and cook healthier meals, to the best of our knowledge then, but it would usually spoil and go to waste because we couldn’t fight off the craving, leaving us to eating out or ordering in from the local pizza shop.
“My lifestyle was a far cry from anything resembling healthy. As a kid, I’d always been the skinny, scrawny one in the crowd—lanky and light. But as I transitioned into adulthood, that changed.
“Laziness crept in, and I stopped paying attention to what I was putting into my body—food and alcohol became thoughtless habits. The heaviest I ever got was 210 pounds (95 kilos), a number that still jolts me when I think about it.
“Growing up, I hovered around 150 pounds (68 kilos), so ballooning to over a third more than my norm was a shocking departure. I’d flip through old photos from my early twenties, struck by how slim I once was, almost missing that version of myself.
“Clothes told the story too—I went from slipping comfortably into medium shirts to squeezing into them, eventually surrendering to a wardrobe of larger sizes that felt foreign.
“At the peak of this unhealthy shift, I’d layer up in oversized sweatshirts even in the sweltering 90-degree summers, not *** Local Caption *** 47
(c) Dukas -
