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  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_010.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_004.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_026.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_016.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_047.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_044.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_042.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_040.jpg
  • Kourtney Kardashian arrives at the PrettyLittleThing By Kourtney Kardashian Launch held at Poppy on October 25, 2017 in West Hollywood, California. 25 Oct 2017 Pictured: Kourtney Kardashian. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA106185_043.jpg
  • Rachel Bilson arrives at the 2017 Baby2Baby Gala held at 3LABS on November 11, 2017 in Culver City, California. 11 Nov 2017 Pictured: Rachel Bilson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA115489_009.jpg
  • Julia Roberts arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Julia Roberts. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99780_003.jpg
  • Julia Roberts arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Julia Roberts. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99780_005.jpg
  • Kate Hudson wearing David Koma arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Kate Hudson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99779_022.jpg
  • Kate Hudson wearing David Koma arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Kate Hudson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99779_033.jpg
  • Nina Dobrev arrives at the Los Angeles Premiere Of Columbia Pictures' 'Flatliners' held at The Theatre at Ace Hotel on September 27, 2017 in Los Angeles, California. 27 Sep 2017 Pictured: Nina Dobrev. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91156_005.jpg
  • Nina Dobrev arrives at the Los Angeles Premiere Of Columbia Pictures' 'Flatliners' held at The Theatre at Ace Hotel on September 27, 2017 in Los Angeles, California. 27 Sep 2017 Pictured: Nina Dobrev. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91156_036.jpg
  • Lily Collins wearing a Reem Acra dress with Djula and Maxior jewelry arrives at the Los Angeles Premiere Of Amazon Studios' 'The Last Tycoon' held at the Harmony Gold Preview House and Theater on July 27, 2017 in Hollywood, California. 27 Jul 2017 Pictured: Lily Collins. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA61157_002.jpg
  • Lily Collins wearing a Reem Acra dress with Djula and Maxior jewelry arrives at the Los Angeles Premiere Of Amazon Studios' 'The Last Tycoon' held at the Harmony Gold Preview House and Theater on July 27, 2017 in Hollywood, California. 27 Jul 2017 Pictured: Lily Collins. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    RTIMEGA61157_016.jpg
  • Rachel Bilson arrives at the 2017 Baby2Baby Gala held at 3LABS on November 11, 2017 in Culver City, California. 11 Nov 2017 Pictured: Rachel Bilson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA115489_007.jpg
  • Rachel Bilson arrives at the 2017 Baby2Baby Gala held at 3LABS on November 11, 2017 in Culver City, California. 11 Nov 2017 Pictured: Rachel Bilson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA115489_006.jpg
  • Julia Roberts arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Julia Roberts. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99780_002.jpg
  • Kate Hudson wearing David Koma arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Kate Hudson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99779_004.jpg
  • Kate Hudson wearing David Koma arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Kate Hudson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99779_008.jpg
  • Kate Hudson wearing David Koma arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Kate Hudson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99779_028.jpg
  • Kate Hudson wearing David Koma arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Kate Hudson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99779_032.jpg
  • Nina Dobrev arrives at the Los Angeles Premiere Of Columbia Pictures' 'Flatliners' held at The Theatre at Ace Hotel on September 27, 2017 in Los Angeles, California. 27 Sep 2017 Pictured: Nina Dobrev. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91156_022.jpg
  • Nina Dobrev arrives at the Los Angeles Premiere Of Columbia Pictures' 'Flatliners' held at The Theatre at Ace Hotel on September 27, 2017 in Los Angeles, California. 27 Sep 2017 Pictured: Nina Dobrev. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91156_021.jpg
  • Nina Dobrev arrives at the Los Angeles Premiere Of Columbia Pictures' 'Flatliners' held at The Theatre at Ace Hotel on September 27, 2017 in Los Angeles, California. 27 Sep 2017 Pictured: Nina Dobrev. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91156_032.jpg
  • Tyra Banks arrives at NBC's 'America's Got Talent' Season 12 Live Show held at Dolby Theatre on August 15, 2017 in Hollywood, California. 15 Aug 2017 Pictured: Tyra Banks. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA68611_003.jpg
  • Tyra Banks arrives at NBC's 'America's Got Talent' Season 12 Live Show held at Dolby Theatre on August 15, 2017 in Hollywood, California. 15 Aug 2017 Pictured: Tyra Banks. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA68611_010.jpg
  • Tyra Banks arrives at NBC's 'America's Got Talent' Season 12 Live Show held at Dolby Theatre on August 15, 2017 in Hollywood, California. 15 Aug 2017 Pictured: Tyra Banks. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA68611_012.jpg
  • Mel B wearing a bejewelled sheer sequined bodysuit arrives at NBC's 'America's Got Talent' Season 12 Live Show held at Dolby Theatre on August 15, 2017 in Hollywood, California. 15 Aug 2017 Pictured: Mel B, Melanie Brown. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA68604_010.jpg
  • Mel B wearing a bejewelled sheer sequined bodysuit arrives at NBC's 'America's Got Talent' Season 12 Live Show held at Dolby Theatre on August 15, 2017 in Hollywood, California. 15 Aug 2017 Pictured: Mel B, Melanie Brown. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA68604_015.jpg
  • Lily Collins wearing a Reem Acra dress with Djula and Maxior jewelry arrives at the Los Angeles Premiere Of Amazon Studios' 'The Last Tycoon' held at the Harmony Gold Preview House and Theater on July 27, 2017 in Hollywood, California. 27 Jul 2017 Pictured: Lily Collins. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA61157_007.jpg
  • Lily Collins wearing a Reem Acra dress with Djula and Maxior jewelry arrives at the Los Angeles Premiere Of Amazon Studios' 'The Last Tycoon' held at the Harmony Gold Preview House and Theater on July 27, 2017 in Hollywood, California. 27 Jul 2017 Pictured: Lily Collins. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA61157_011.jpg
  • Rachel Bilson arrives at the 2017 Baby2Baby Gala held at 3LABS on November 11, 2017 in Culver City, California. 11 Nov 2017 Pictured: Rachel Bilson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA115489_010.jpg
  • Julia Roberts arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Julia Roberts. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99780_017.jpg
  • Kate Hudson wearing David Koma arrives at the amfAR Inspiration Gala Los Angeles 2017 held at Ron Burkle's Green Acres Estate on October 13, 2017 in Beverly Hills, California. 13 Oct 2017 Pictured: Kate Hudson. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA99779_042.jpg
  • Nina Dobrev arrives at the Los Angeles Premiere Of Columbia Pictures' 'Flatliners' held at The Theatre at Ace Hotel on September 27, 2017 in Los Angeles, California. 27 Sep 2017 Pictured: Nina Dobrev. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91156_001.jpg
  • Nina Dobrev arrives at the Los Angeles Premiere Of Columbia Pictures' 'Flatliners' held at The Theatre at Ace Hotel on September 27, 2017 in Los Angeles, California. 27 Sep 2017 Pictured: Nina Dobrev. Photo credit: IPA/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA91156_019.jpg
  • HOLLYWOOD, LOS ANGELES, CA, USA - NOVEMBER 14: Rapper Cardi B (Belcalis Marlenis Almanzar) arrives at the Fashion Nova x Cardi B Collaboration Launch Event held at Boulevard3 on November 14, 2018 in Hollywood, Los Angeles, California, United States. 14 Nov 2018 Pictured: Cardi B, Belcalis Marlenis Almanzar. Photo credit: Xavier Collin/Image Press Agency/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA308094_007.jpg
  • HOLLYWOOD, LOS ANGELES, CA, USA - NOVEMBER 14: Rapper Cardi B (Belcalis Marlenis Almanzar) arrives at the Fashion Nova x Cardi B Collaboration Launch Event held at Boulevard3 on November 14, 2018 in Hollywood, Los Angeles, California, United States. 14 Nov 2018 Pictured: Cardi B, Belcalis Marlenis Almanzar. Photo credit: Xavier Collin/Image Press Agency/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA308094_027.jpg
  • HOLLYWOOD, LOS ANGELES, CA, USA - NOVEMBER 14: Rapper Cardi B (Belcalis Marlenis Almanzar) arrives at the Fashion Nova x Cardi B Collaboration Launch Event held at Boulevard3 on November 14, 2018 in Hollywood, Los Angeles, California, United States. 14 Nov 2018 Pictured: Cardi B, Belcalis Marlenis Almanzar. Photo credit: Xavier Collin/Image Press Agency/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA308094_040.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_004.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_002.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_008.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_006.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_007.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_003.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_005.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_009.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_011.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_010.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
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