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  • June 1, 2017 - Kolkata, West Bengal, India - Indian  labourers pushes a hand cart loaded with Iron material and  cross the howrah bridge in  Kolkata on June 1, 2017.  India's economic growth slowed to 7.1 percent for the 2016-17 financial year,Growth for the 12 months ended March 31 was well below a revised figure of eight percent for the previous year, and follows the government's shock move last November to ban most of the currency in circulation. (Credit Image: © Debajyoti Chakraborty/NurPhoto via ZUMA Press)
    A20170601_zaa_n230_109.jpg
  • August 16, 2017 - Ankara, Turkey - A 23-year-old unemployment man holds a 5 Turkish Lira banknote in Ankara, Turkey on August 16, 2017. Turkey's youth unemployment rate for people aged 15-24 was 19.8 percent, with a 2.4 percentage point increase in May compared to the same period of 2016. The Turkish Statistical Institute (TurkStat) had reported that the number of jobless people aged 15 and above jumped to 3.2 million in May, marking an increase of 330,000 from the same month last year. (Credit Image: © Altan Gocher/NurPhoto via ZUMA Press)
    RTIRTI20170816_zaa_n230_185.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_004.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_002.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_003.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_007.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_006.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_008.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_005.jpg
  • EXCLUSIVE: SHOCKING IMAGES OF CAPE TOWN’S BONE-DRY DAM WHERE ONCE LOCALS USED TO GO BOATING AND WATER SKIING WITH PIX By Magnus News Agency Shocking images show a bone-dry desert where once boats used to sail on a reservoir as drought continues to ravage South Africa. Theewaterskloof Dam once hosted yacht clubs and water skiing but today not even one vessel could be launched on the parched space. Photographer Dirk Theron visited the starved body of water last week and took these frightening images of the dried-up lake which should supply 40 percent of the water to Cape Town’s four million residents. As Dirk’s pictures show, skeletons of fish and muddy pools are much of what remains of the former 480 million cubic metre capacity site. Last week billionaire former New York Mayor Michael Bloomberg toured Theewaterskloof as part of his role as UN special Envoy for Climate Action. He warned the reservoir and draught across the Western Cape should act as a wake-up call for the international community on climate change. Despite the drought, which has struck the area for the past few years, government officials in South Africa have been criticised for their handling of the crisis. A ‘Day Zero’ when municipal taps would be turned off has been pushed back from June 4 to July 9 despite chronic shortages continuing. South African Dirk lives just 30 minutes from Theewaterskloof, but said he was stunned by what he found there. He said: “Theewaterskloof dam is one of those places where everybody has a boat and people would go there for the weekend. “A friend of mine used to be a member of the Theewaters sports club, we used to go there all the time water skiing and playing on the water in his boat. “This was a massive, massive body of water. It’s been a few years since last I’ve been there but when I saw it I was shocked to my core. “We all know about the water crisis but standing there and seeing it with your own eyes is so surreal. “I stood on dry ground
    MEGA180787_001.jpg
  • April 4, 2017 - Sofia, Bulgaria - Public protest in front of the Energy and Water Regulatory Commission (EWRC) in Sofia, on April 4, 2017 against the proposed increase in the price of heating energy by over 20 percent after the gas prices have risen by 30 percent since the beginning of April. (Credit Image: © Hristo Vladev/NurPhoto via ZUMA Press)
    20170404_zaa_n230_119.jpg
  • April 30, 2019 - Kiev, Ukraine - Tetiana Slipachuk, Chairman of the Central Election Commission, (L) speaks during a  session with the officially announce the results of the presidential election at the commission headquarters in Kiev, Ukraine, on 30 April, 2019. According to the results processed of 100 percent of the protocols, Ukrainian comedian actor Volodymyr Zelenskiy won the presidential election in the second round by collecting 73.22 percent of the voters, while the incumbent head of state Petro Poroshenko, received 24.45% (Credit Image: © Str/NurPhoto via ZUMA Press)
    20190430_zaa_n230_081.jpg
  • **PREMIUM EXCLUSIVE** Noah Cyrus attends a fundraiser held at Gerard Butler's home for the Malibu Fire Relief in West Hollywood. Noah was seen leaving Gerard's house with a male companion. Her sister Miley Cyrus lost her Malibu home due to the raging wildfires. Butler, Miley and Robin Thicke, were among thousands who lost their homes to the blazes, which have killed at least 74 people across the state. Up to a thousand are still unaccounted for. The 300 star invited his A-list friends to his West Hollywood home for the cause, hoping to raise at least $1million for fire relief. Remains of at least 74 people have been recovered so far in California. 71 of the victims are from the Camp Fire around the Sierra foothills hamlet of Paradise and three are from the Woolsey Fire near Los Angeles. Of the dead, 13 victims are yet to be identified. The once picturesque town was home to nearly 27,000 residents before it was largely incinerated by the deadly Camp Fire on the night of November 8. More than a week later, a team of more than 9,000 firefighters have managed to carve containment lines around 45 percent of the blaze's perimeter, up from 35 percent a day earlier. The powerful fire razed through more than 142,000 acres in a little over a week. Nearly 12,000 homes and buildings, including most of the town of Paradise, were incinerated hours after the blaze erupted, the California Department of Forestry and Fire Protection (Cal Fire) has said. Thousands of additional structures are still threatened by the Camp Hill fire, and as many as 50,000 people were under evacuation orders at the height of the blaze. 17 Nov 2018 Pictured: Noah Cyrus. Photo credit: Rachpoot/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA309066_010.jpg
  • **PREMIUM EXCLUSIVE** Noah Cyrus attends a fundraiser held at Gerard Butler's home for the Malibu Fire Relief in West Hollywood. Noah was seen leaving Gerard's house with a male companion. Her sister Miley Cyrus lost her Malibu home due to the raging wildfires. Butler, Miley and Robin Thicke, were among thousands who lost their homes to the blazes, which have killed at least 74 people across the state. Up to a thousand are still unaccounted for. The 300 star invited his A-list friends to his West Hollywood home for the cause, hoping to raise at least $1million for fire relief. Remains of at least 74 people have been recovered so far in California. 71 of the victims are from the Camp Fire around the Sierra foothills hamlet of Paradise and three are from the Woolsey Fire near Los Angeles. Of the dead, 13 victims are yet to be identified. The once picturesque town was home to nearly 27,000 residents before it was largely incinerated by the deadly Camp Fire on the night of November 8. More than a week later, a team of more than 9,000 firefighters have managed to carve containment lines around 45 percent of the blaze's perimeter, up from 35 percent a day earlier. The powerful fire razed through more than 142,000 acres in a little over a week. Nearly 12,000 homes and buildings, including most of the town of Paradise, were incinerated hours after the blaze erupted, the California Department of Forestry and Fire Protection (Cal Fire) has said. Thousands of additional structures are still threatened by the Camp Hill fire, and as many as 50,000 people were under evacuation orders at the height of the blaze. 17 Nov 2018 Pictured: Noah Cyrus. Photo credit: Rachpoot/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA309066_007.jpg
  • **PREMIUM EXCLUSIVE** Singer CeeLo Green is spotted attending a fundraiser held at Gerard Butler's house for the Malibu Fire Relief in West Hollywood. Butler, Robin Thicke, and Miley Cyrus were among thousands who lost their homes to the blazes, which have killed at least 74 people across the state. Up to a thousand are still unaccounted for. The 300 star invited his A-list friends to his West Hollywood home for the cause, hoping to raise at least $1million for fire relief. Remains of at least 74 people have been recovered so far in California. 71 of the victims are from the Camp Fire around the Sierra foothills hamlet of Paradise and three are from the Woolsey Fire near Los Angeles. Of the dead, 13 victims are yet to be identified. The once picturesque town was home to nearly 27,000 residents before it was largely incinerated by the deadly Camp Fire on the night of November 8. More than a week later, a team of more than 9,000 firefighters have managed to carve containment lines around 45 percent of the blaze's perimeter, up from 35 percent a day earlier. The powerful fire razed through more than 142,000 acres in a little over a week. Nearly 12,000 homes and buildings, including most of the town of Paradise, were incinerated hours after the blaze erupted, the California Department of Forestry and Fire Protection (Cal Fire) has said. Thousands of additional structures are still threatened by the Camp Hill fire, and as many as 50,000 people were under evacuation orders at the height of the blaze. 17 Nov 2018 Pictured: CeeLo Green. Photo credit: Rachpoot/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA309068_005.jpg
  • **PREMIUM EXCLUSIVE** Cindy Crawford and Rande Gerber are seen attending a fundraiser held at Gerard Butler's house for the Malibu Fire Relief in West Hollywood. The couple enjoyed themselves at the charity event. They arrived to Gerard's house at 6:30 P.M. and left at 10:15 P.M. Pizza seemed to be the main course at the fundraiser. Cindy is seen holding a slice of pizza in hand as they leave the house. Butler, Robin Thicke, and Miley Cyrus were among thousands who lost their homes to the blazes, which have killed at least 74 people across the state. Up to a thousand are still unaccounted for. The 300 star invited his A-list friends to his West Hollywood home for the cause, hoping to raise at least $1million for fire relief. Remains of at least 74 people have been recovered so far in California. 71 of the victims are from the Camp Fire around the Sierra foothills hamlet of Paradise and three are from the Woolsey Fire near Los Angeles. Of the dead, 13 victims are yet to be identified. The once picturesque town was home to nearly 27,000 residents before it was largely incinerated by the deadly Camp Fire on the night of November 8. More than a week later, a team of more than 9,000 firefighters have managed to carve containment lines around 45 percent of the blaze's perimeter, up from 35 percent a day earlier. The powerful fire razed through more than 142,000 acres in a little over a week. Nearly 12,000 homes and buildings, including most of the town of Paradise, were incinerated hours after the blaze erupted, the California Department of Forestry and Fire Protection (Cal Fire) has said. Thousands of additional structures are still threatened by the Camp Hill fire, and as many as 50,000 people were under evacuation orders at the height of the blaze. 17 Nov 2018 Pictured: Cindy Crawford and Rande Gerber. Photo credit: Rachpoot/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA309073_002.jpg
  • **PREMIUM EXCLUSIVE** Jamie Foxx attends a fundraiser held at Gerard Butler's house for the Malibu Fire Relief in West Hollywood. Jamie came to the charity event with his daughters (Not Pictured). Katie Holmes did not attend the fundraiser with Jamie. Butler, Robin Thicke, and Miley Cyrus were among thousands who lost their homes to the blazes, which have killed at least 74 people across the state. Up to a thousand are still unaccounted for. The 300 star invited his A-list friends to his West Hollywood home for the cause, hoping to raise at least $1million for fire relief. Remains of at least 74 people have been recovered so far in California. 71 of the victims are from the Camp Fire around the Sierra foothills hamlet of Paradise and three are from the Woolsey Fire near Los Angeles. Of the dead, 13 victims are yet to be identified. The once picturesque town was home to nearly 27,000 residents before it was largely incinerated by the deadly Camp Fire on the night of November 8. More than a week later, a team of more than 9,000 firefighters have managed to carve containment lines around 45 percent of the blaze's perimeter, up from 35 percent a day earlier. The powerful fire razed through more than 142,000 acres in a little over a week. Nearly 12,000 homes and buildings, including most of the town of Paradise, were incinerated hours after the blaze erupted, the California Department of Forestry and Fire Protection (Cal Fire) has said. Thousands of additional structures are still threatened by the Camp Hill fire, and as many as 50,000 people were under evacuation orders at the height of the blaze. 17 Nov 2018 Pictured: Jamie Foxx. Photo credit: Rachpoot/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA309077_001.jpg
  • **PREMIUM EXCLUSIVE** Actor Pierce Brosnan attends a fundraiser held at Gerard Butler's house for the Malibu Fire Relief in West Hollywood. A few days ago, Pierce went to Malibu to assess the damage that was done to his property due to the raging wildfires that swept through Malibu. Butler, Robin Thicke, and Miley Cyrus were among thousands who lost their homes to the blazes, which have killed at least 74 people across the state. Up to a thousand are still unaccounted for. The 300 star invited his A-list friends to his West Hollywood home for the cause, hoping to raise at least $1million for fire relief. Remains of at least 74 people have been recovered so far in California. 71 of the victims are from the Camp Fire around the Sierra foothills hamlet of Paradise and three are from the Woolsey Fire near Los Angeles. Of the dead, 13 victims are yet to be identified. The once picturesque town was home to nearly 27,000 residents before it was largely incinerated by the deadly Camp Fire on the night of November 8. More than a week later, a team of more than 9,000 firefighters have managed to carve containment lines around 45 percent of the blaze's perimeter, up from 35 percent a day earlier. The powerful fire razed through more than 142,000 acres in a little over a week. Nearly 12,000 homes and buildings, including most of the town of Paradise, were incinerated hours after the blaze erupted, the California Department of Forestry and Fire Protection (Cal Fire) has said. Thousands of additional structures are still threatened by the Camp Hill fire, and as many as 50,000 people were under evacuation orders at the height of the blaze. 17 Nov 2018 Pictured: Pierce Brosnan. Photo credit: Rachpoot/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA309080_003.jpg
  • April 30, 2017 - Rome, Italy - About two million Democratic Party (Pd) militants have gone to the polls to vote for the new party secretary. With over 70 percent of preferences wins and returns to the leadership of the Democratic Party Matteo Renzi. In the photos, the PD gazebo set up at Termini Station. (Credit Image: © Patrizia Cortellessa/Pacific Press via ZUMA Wire)
    RTI20170430_zaa_p133_270.jpg
  • Lili Reinhart shows off her wild side in a stunning photo shoot for The Mighty Company. The Netflix star set pulses racing as she posed in a number of revealing outfits as she was unveiled as the face of The Mighty Company x Ilaria Urbinati campaign. In the snaps, Lili, 22, can be seen wearing just her underwear paired with a pink cowboy hat and metallic silver bomber jacket. She was also snapped wearing a black PVC ensemble. The theme of the photo shoot, Jessie Willner of The Mighty Company, said: 'was space cowgirl themed as a tongue-in-cheek embodiment of a wild, independent woman in a galactic setting. 'Ilaria pulled up the September 1995 Rolling Stone cover of Alicia Silverstone, and we had to shoot a nod to it. Lili was the perfect front-woman of this because she's this incredibly outspoken champion of women." Amazingly 100 percent of the profits from the collaborative campaign will be donated to a charity that helps to stop forced and child marriages. 07 Dec 2018 Pictured: Lili Reinhart. Photo credit: The Mighty Company / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA320713_001.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_002.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_004.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_007.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_005.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_008.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_010.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_011.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_017.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_015.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_020.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_021.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_022.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_024.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_023.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_025.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_028.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_030.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_033.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_031.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_032.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_035.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_036.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_039.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_001.jpg
  • A shopper carrying Tesco bags. Tesco is currently the 8th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488423.jpg
  • A mobile phone connected to the Vodafone network. Vodafone is currently the 2nd most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488419.jpg
  • General view of a British Telecom Homehub router, along with a telephone. BT is currently the 4th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488421.jpg
  • General view of an O2 mobile phone shop in Islington, London. O2 is currently the 9th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488418.jpg
  • A mobile phone connected to the Vodafone network. Vodafone is currently the 2nd most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488415.jpg
  • General view of a Shell garage in Crouch End, north London. Shell is currently the most valuable British brand, according to analysts Brand Finance's directory. Picture date: Thursday March 9, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488412.jpg
  • HSBC debit cards, credit card and online banking verifier. HSBC is currently the 3rd most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488410.jpg
  • A Barclays Bank cheque book, online banking PINSentry and cheque book. Barclays is currently the 6th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488409.jpg
  • General view of a Shell garage in Crouch End, north London. Shell is currently the most valuable British brand, according to analysts Brand Finance's directory. Picture date: Thursday March 9, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488408.jpg
  • General view of a BP garage in Hornsey, north London. BP is currently the 5th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Thursday March 9, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488398.jpg
  • Petrol pumps in a BP garage in Hornsey, north London. BP is currently the 5th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Thursday March 9, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488405.jpg
  • General view of a British Telecom Homehub router, along with a telephone. BT is currently the 4th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488395.jpg
  • Petrol pumps in a BP garage in Hornsey, north London. BP is currently the 5th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Thursday March 9, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488405.jpg
  • General view of a British Telecom Homehub router, along with a telephone. BT is currently the 4th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488395.jpg
  • Petrol pumps at a Shell garage in Crouch End, north London. Shell is currently the most valuable British brand, according to analysts Brand Finance's directory. Picture date: Thursday March 9, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488399.jpg
  • A mobile phone connected to the Vodafone network. Vodafone is currently the 2nd most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488419.jpg
  • General view of a British Telecom Homehub router, along with a telephone. BT is currently the 4th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488421.jpg
  • General view of an O2 mobile phone shop in Islington, London. O2 is currently the 9th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488418.jpg
  • A mobile phone connected to the Vodafone network. Vodafone is currently the 2nd most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488415.jpg
  • General view of a Shell garage in Crouch End, north London. Shell is currently the most valuable British brand, according to analysts Brand Finance's directory. Picture date: Thursday March 9, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488412.jpg
  • HSBC debit cards, credit card and online banking verifier. HSBC is currently the 3rd most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488414.jpg
  • A Barclays Bank cheque book, online banking PINSentry and cheque book. Barclays is currently the 6th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488413.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_021.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_005.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_018.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_013.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_014.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_015.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_017.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_020.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_002.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_003.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_006.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_010.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_007.jpg
  • EXCLUSIVE: ARE YOU SWAY-ED BY THIS UNIQUE HOUSE FOR SALE - INCREDIBLE HOME INSIDE A 220-FOOT TOWER COULD BE YOURS FOR £10 By Magnus News Agency Buyers are being offered one last chance to own a unique 220-foot-high Victorian folly before it is offered as a prize in a competition for just £10 a ticket. Sway Tower, in Hampshire, sits resplendent above the village of the same name with commanding views of the English countryside and south coast. The 1880s intricately designed concrete monolith has been in the family of businessman and entrepreneur Paul Atlas and his family for the past 45 years. But now the property, which comes complete with a 60-foot swimming pool and telecommunications income of £35,000 plus a year, is on the market in a once-in-a-lifetime sale. Grandfather-of-four Paul has lived in the 14-floor tower since 1995 with Julie raising their two children. Since they bought it in 1973 for £2,600 the Atlas’s have been busy renovating the structure ensuring that what stands now will last for generations to come. In the mid-90s, with the backing of the local authority and heritage charities, Paul and a team of tradesmen renovated the structure after the storm of 1987 hit the south coast. Over the years the Atlas family has used the tower for a variety of uses; from a very elaborate ‘shed’ when it was first purchased, to a restaurant, hotel and finally to a one-of-a-kind multi-million-pound home. However, if a buyer cannot be found within 45 days, the owners will commence the process of offering the tower as prize with competition property experts WinThis.life Paul, 71, said the tower is anything but an ordinary home and nowadays he restricts climbing the 330 steps to the top to once a month. He said offering the chance for someone to own the tower for the price of a raffle ticket was an incredible opportunity as the place is ready to go needing no work by any new owner. Paul said: “In the early 1990s we were taking £585 a night in revenue from t
    MEGA179323_004.jpg
  • August 19, 2017 - Bydgoszcz, Poland - A Ferrari F430 is seen in the old center of the city on 19 August, 2017. (Credit Image: © Jaap Arriens/NurPhoto via ZUMA Press)
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  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_003.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_006.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_009.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_013.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_012.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_014.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_018.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_016.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_019.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_026.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_027.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_029.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_034.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_037.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_038.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_040.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_041.jpg
  • HSBC debit cards, credit card and online banking verifier. HSBC is currently the 3rd most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
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  • A Barclays Bank cheque book, online banking PINSentry and cheque book. Barclays is currently the 6th most valuable British brand, according to analysts Brand Finance's directory. Picture date: Friday March 10, 2017. Photo credit should read: Matt Crossick/ EMPICS Entertainment.
    PA-30488413.jpg
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