• Facebook
  • Twitter
x

RealTime Images

  • Portfolio
  • About
  • Contact
  • Video
  • Blog
  • Archive
Show Navigation
Cart Lightbox Client Area

Search Results

Refine Search
Match all words
Match any word
Prints
Personal Use
Royalty-Free
Rights-Managed
(leave unchecked to
search all images)
Next
{ 111 images found }
twitterlinkedinfacebook

Loading ()...

  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_006.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_007.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_001.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_002.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_004.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_003.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_008.jpg
  • EXCLUSIVE: A 10-year-old girl suffering from a rare skin disorder is gradually turning into a stone. Scutes shaped as barks -- caused due to mutation of genes -- have spread all over her body. Rajeshwari, hailing from a tribal area in Dantewada district of north Indian state of Chhattisgarh suffers from a case of ichthyosis that causes reddening, scaling and severe blistering of the skin. The incurable disease affects the process of skin regeneration in the human body, making it hard and flaky. Visuals show a heart-wrenching sight of Rajeshwari sitting under a thatched hut with blisters almost covering her whole body. Though the disease doesn't pose any risk to her life, it has made a life 'a living hell'. The disease hinders her daily life, making even simple activities such as walking and sitting very painful. According to reports, the rare genetic condition affects very few people and till now only two dozen cases have been reported in the world. The rarity of the case makes research difficult and the medicine to control the incurable disease has severe side effects. For people residing in the Naxal infested area, availing simple health care is already a mean feat and Rajeshwari's condition requires her to travel to a big city which is difficult for the time being. when doctors were shown the patient's case file, few of them came forward to express their opinions and diagnosis. Speaking about her condition, Dr.Satyaki Ganguly, Associate Professor at All India Institute of Medical Sciences(AIIMS), Raipur, said “ The medical term for this genetic disorder is Ichthyosis Psoriasis and due to very few cases in India, there has not been any major breakthrough in terms of research. Currently, science has no cure for this ailment.” Another dermatologist has another take on Rajeshwari’s case, Dr.Yash Upender from Dantewada Hospital believes that the girl suffers from Epidermolytic Ichthyosis which is not a life threatening disease but is still uncurable. Medication
    MEGA586418_005.jpg
  • June 24, 2017 - London, UK - London, UK. 24th September 2017. Two of the around 40 EDL protesters get their flag ready outside the Wetherspoons pub on Whitehall. Later police escorted them to Charing Cross and down a backstreet to the Embankment where they were to hold a rally. Earlier police had moved several hundred anti-fascist counter-protesters organised by UAF from their route down to a separate area of the Embankment a short distance away where they continued to protest noisily against the EDL until the police escorted them back to Charing Cross station. Both EDL and UAF had conditions for their protests imposed on them under Section 12 and 14 of the Public Order Act, 1986, due to concerns of serious public disorder, and disruption to the community. Peter Marshall ImagesLive (Credit Image: © Peter Marshall/ImagesLive via ZUMA Wire)
    20170624_zap_d99_021.jpg
  • May 8, 2017 - Lahore, Punjab, Pakistan - Thalassaemia is an inherited blood disorder and can be simply stated as the inability of the body to produce adequate amount of Hemoglobin in the red blood cells. (Credit Image: © Rana Sajid Hussain/Pacific Press via ZUMA Wire)
    RTI20170508_zaa_p133_001.jpg
  • May 1, 2019 - Paris, France - People protest during the annual May Day protests on May 01, 2019 in Paris, France. More than 7,400 police and security forces have been deployed in the city to prevent a repeat of the violence and disorder seen in 2018. (Credit Image: © Estelle Ruiz/NurPhoto via ZUMA Press)
    20190501_zaa_n230_607.jpg
  • March 3, 2016 - London, London, UK - A replica belt worn by Muhammed Ali after he won a fight against  Sonny Liston in 1964. The belt features in the  I Am The Greatest  - Muhammad Ali Exhibition.  Exhibition featuring more than 100 artefacts from the boxer's career, put together with the help of the Ali family, showcased to celebrate the life of the former heavyweight champion giving an insight into one of the sport's most famous personalities. London, UK. (Credit Image: © Ray Tang/London News Pictures via ZUMA Wire)
    20160303_zaf_l94_017.jpg
  • Dec 17, 2008 - Anaheim Hills, California, USA - Muhammad Ali was always Art Tinajero's hero, but after a chance meeting with the champ he became a 'life-long fan.' A kind stranger helped arrange an impromptu meeting with Ali who graciously invited the fan to lunch. A 1964 picture of Ali defeating Liston is prominently displayed in Tinajero's Anaheim Hillls home.    (Credit Image: © The Orange County Register/ZUMA Press)
    20081217_zaf_o44_097.jpg
  • December 1, 1981 - Washington, District of Columbia, U.S. - U.S. President Ronald Wilson Reagan's, Vice-President GEORGE HERBERT WALKER BUSH smiling with his arms folded. (Credit Image: © Michael A. W. Evans/ZUMAPRESS.com)
    19811201_rua_e04_330.jpg
  • July 17, 1977 - Michigan, U.S. - Twelfth Street is pictured under a cloud of smoke during the rioting in 1967. Errant flames of the 1967 riot swept into residential sections destroying solid homes of longtime residents. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_309.jpg
  • July 9, 1992 - Michigan, U.S. - Detroit Riot of 1967, a scene on 12th Street. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_311.jpg
  • February 2, 2017 - Michigan, U.S. - National Guardsman Gary Ciko of Hamtramck checks on buildings for snipers during the riot on July 23,1967 in Detroit. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_314.jpg
  • February 2, 2017 - Michigan, U.S. - Detroit Riot of 1967, a scene on 12th Street. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_315.jpg
  • July 24, 1967 - Michigan, U.S. - Burned out shells are all that remain of former houses and businesses in the area of the Detroit, Michigan race riot in 1967. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_304.jpg
  • July 23, 1967 - Michigan, U.S. - The streets of Detroit during the 1967 riot. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_303.jpg
  • June 23, 1987 - Michigan, U.S. - The charred remains of a building destroyed in the 1967 riot in Detroit. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_310.jpg
  • July 25, 1967 - Michigan, U.S. - Troops are assembled at Detroit Police headquarters on Beaubien in downtown Detroit during the riot in Detroit in 1967. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_306.jpg
  • June 24, 2017 - London, UK - London, UK. 24th September 2017. Several hundred attended Unite Against Fascism's protest against the EDL, some gathering on the corner of Northumberland Avenue close to the advertised WDL meeting point at Charing Cross where only a handful of the EDL turned up, with rather more meeting at the Wetherspoons on Whitehall. There were a few minor scuffles with EDL protesters on their way to the pub, but several hundred police kept the two groups apart, moving the UAF down to their assigned rally point on the Embankment before escorting the EDL to another location a couple of hundred yards away. After the EDL had been escorted back to the station, the UAF marched to join the women's rally at Downing St against Theresa May's collusion with the UDP to prop up her minority government. Peter Marshall ImagesLive (Credit Image: © Peter Marshall/ImagesLive via ZUMA Wire)
    20170624_zap_d99_001.jpg
  • October 23, 2004 - Beverly Hills, California, U.S. - Sports legend MUHAMMAD ALI embraces actress BRITTANY MURPHY at ''Mercedes-Benz Presents The 16th Annual Carousel of Hope Benefitting the Barbara Davis Center For Childhood Diabetes''. (Credit Image: © Starmax/Newscom via ZUMA Press)
    20160604_zaa_nc34_025.jpg
  • A 1964 picture of Ali defeating Liston (left) and a charcoal portrait of Ali, 18, is prominently displayed in Art Tinajero's Anaheim Hillls home. A father's day gift from his sons and a fortunate set of circumstances ended in the most memorable meeting of his life in 1991.  //ADDITIONAL INFO: Mr. Tinajero has written a fine True Life about a chance lunch with Muhammad Ali.   Tinajero but after a chance meeting with the champ he became a ''life-long fan.'' Ali graciously invited him to lunch after the fan asked for an autograph. true_ali.1231.cy  - 121708 CINDY YAMANAKA, THE ORANGE COUNTY REGISTER - CQ's (Credit Image: © The Orange County Register/ZUMAPRESS.com)
    20081217_zaf_o44_092.jpg
  • July 30, 1967 - Michigan, U.S. - Riot Detroit 1967 Troops on Linwood Ave. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_307.jpg
  • June 20, 2017 - Michigan, U.S. - While a policeman stands guard, the body of an unidentfied msn is removed from the burned out ruins of as building on Seward and Twelfth in the riot area in Detroit in 1967. Another man, also unidentified, was found dead in the rubble. The cause of their death ha not yet been officially determined. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_316.jpg
  • July 9, 1992 - Michigan, U.S. - Lt. General John Throckmorton takes to the field with his paratroopers in riot-torn Detroit on July 25, 1967. Throckmorton is commander of the 4,700 troops sent to Detroit by President Johnson to quell the outbreak. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_312.jpg
  • December 28, 1967 - Michigan, U.S. - The flames of riot leave so little for their victims. For Emma Jean Woolford it was only bedsprings and a headboard dragged desperately from her blazing home to safety at Boston Blvd snd Linwood in Detroit on Sunday, July 23, 1967. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_308.jpg
  • November 17, 2016 - Michigan, U.S. - Bullet holes in a building on 12th street during the 1967 Detroit riot. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_313.jpg
  • July 25, 1967 - Michigan, U.S. - African Americans during the riot in Detroit in 1967. (Credit Image: © Detroit Free Press via ZUMA Wire)
    20170712_sha_f31_305.jpg
  • June 24, 2017 - London, United Kingdom - Several hundred attended Unite Against Fascism's protest against the EDL, some gathering on the corner of Northumberland Avenue close to the advertised WDL meeting point at Charing Cross where only a handful of the EDL turned up, with rather more meeting at the Wetherspoons on Whitehall. There were a few minor scuffles with EDL protesters on their way to the pub, but several hundred police kept the two groups apart, moving the UAF down to their assigned rally point on the Embankment before escorting the EDL to another location a couple of hundred yards away. After the EDL had been escorted back to the station, the UAF marched to join the women's rally at Downing St against Theresa May's collusion with the UDP to prop up her minority government. Peter Marshall ImagesLive (Credit Image: © Peter Marshall/ImagesLive via ZUMA Wire)
    20170624_zap_d99_001.jpg
  • April 28, 2017 - Rio De Janeiro, Rio De Janeiro, Brazil - A street merchant looks on as a metro Rio truck burns in downtown Rio De Janeiro Brazil, Friday 28th April. Large scale protests took place throughout Brazil against the governments planed  changes to workers rights. (Credit Image: © Ch Gardiner/Pacific Press via ZUMA Wire)
    RTI20170428_zaa_p133_346.jpg
  • October 13, 2017 - Rome, Italy - Students protest across Italy Friday against job-placement schemes and against entry exams, as well as demanding more resources for underfunded state schools to boost lessons and keep rundown buildings in a better state of repair in Rome, Italy, on 13 October 2017. (Credit Image: © Andrea Ronchini/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_358.jpg
  • October 13, 2017 - Rome, Italy - Students protest across Italy Friday against job-placement schemes and against entry exams, as well as demanding more resources for underfunded state schools to boost lessons and keep rundown buildings in a better state of repair in Rome, Italy, on 13 October 2017. (Credit Image: © Andrea Ronchini/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_358.jpg
  • October 13, 2017 - Naples, Campania, Italy - Thousands of students held a demonstration, as part of a nationwide mobilization, to protest against the so-called 'La Buona Scuola' (Good School) reform, the school-work alternation and in defence of public education in Naples. (Credit Image: © Paolo Manzo/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_050.jpg
  • October 13, 2017 - Rome, Italy - Thousands of students held a demonstration, as part of a nationwide mobilization, to protest against the so-called Good School reform, the school-work alternation and in defence of public education in Rome, Italy on October 13. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_036.jpg
  • October 13, 2017 - Naples, Campania, Italy - Thousands of students held a demonstration, as part of a nationwide mobilization, to protest against the so-called 'La Buona Scuola' (Good School) reform, the school-work alternation and in defence of public education in Naples, Italy on October 13. (Credit Image: © Paolo Manzo/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_053.jpg
  • October 13, 2017 - Naples, Campania, Italy - Thousands of students held a demonstration, as part of a nationwide mobilization, to protest against the so-called 'La Buona Scuola' (Good School) reform, the school-work alternation and in defence of public education in Naples, Italy. (Credit Image: © Paolo Manzo/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_043.jpg
  • October 13, 2017 - Naples, Campania, Italy - Thousands of students held a demonstration, as part of a nationwide mobilization, to protest against the so-called 'La Buona Scuola' (Good School) reform, the school-work alternation and in defence of public education in Naples, Italy on October 13. (Credit Image: © Paolo Manzo/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_037.jpg
  • October 3, 2017 - Rome, Italy - Italian precarious researchers held a demonstration in front of the Ministry of Economy and Finance to denounce the European Union's economic policies and to claim the recruitment of 10,000 precarious workers in Rome, Italy on October 03, 2017. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    RTI20171003_zaa_n230_185.jpg
  • June 24, 2017 - Rome, Italy - Thousands of members of Italian far-right movement CasaPound from all over Italy march with flags and shout slogans during a demonstration to protest against the 'Ius Soli' in Rome. The 'Ius Soli' is the right of anyone born in the territory of a state to nationality or citizenship. (Credit Image: © Giuseppe Ciccia/Pacific Press via ZUMA Wire)
    RTI20170624_zaa_p133_308.jpg
  • June 22, 2017 - Rome, Italy - Supporters of political party Forza Italia (Go, Italy!) take part in a rally to protest against Rome's Mayor Virginia Raggi in Rome, Italy on June 22, 2017. Several hundred people gathered in Capitol Hill Square to protest against Mayor of Rome Virginia Raggi and her policy after one year of the Five Star government. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    20170622_zaa_n230_138.jpg
  • June 22, 2017 - Rome, Italy - Supporters of political party Forza Italia (Go, Italy!) take part in a rally to protest against Rome's Mayor Virginia Raggi. Several hundred people gathered in Capitol Hill Square to protest against Mayor of Rome Virginia Raggi and her policy after one year of the Five Star government. (Credit Image: © Giuseppe Ciccia/Pacific Press via ZUMA Wire)
    20170622_zaa_p133_122.jpg
  • June 17, 2017 - Rome, Italy - CGIL, Italian trade union, calls for a demonstration to protest against the reintroduction of a new type of work 'voucher' system, coupons to pay jobs for less, that were abolished last March with an amendment of the Government in Rome, Italy on June 17, 2017. (Credit Image: © Giuseppe Ciccia/Pacific Press via ZUMA Wire)
    20170617_zaa_p133_127.jpg
  • October 22, 2016 - Rome, Italy - Thousands of people shout slogans and wave flags as they take to the streets to protest Prime Minister Matteo Renzi's government politics and to say 'NO' at the upcoming constitutional referendum in Rome, Italy. (Credit Image: © Giuseppe Ciccia/Pacific Press via ZUMA Wire)
    20161022_zaa_p133_233.JPG
  • October 22, 2016 - Rome, Italy - Thousands of people shout slogans and wave flags as they take to the streets to protest Prime Minister Matteo Renzi's government politics and to say 'NO' at the upcoming constitutional referendum in Rome, Italy, on 22 October 2016. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    20161022_zaa_n230_113.JPG
  • October 22, 2016 - Rome, Italy - Thousands of people shout slogans and wave flags as they take to the streets to protest Prime Minister Matteo Renzi's government politics and to say 'NO' at the upcoming constitutional referendum in Rome, Italy. (Credit Image: © Giuseppe Ciccia/Pacific Press via ZUMA Wire)
    20161022_zaa_p133_233.JPG
  • October 22, 2016 - Rome, Italy - Thousands of people shout slogans and wave flags as they take to the streets to protest Prime Minister Matteo Renzi's government politics and to say 'NO' at the upcoming constitutional referendum in Rome, Italy, on 22 October 2016. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    20161022_zaa_n230_108.JPG
  • October 13, 2017 - Rome, Italy - Thousands of students held a demonstration, as part of a nationwide mobilization, to protest against the so-called Good School reform, the school-work alternation and in defence of public education in Rome, Italy on October 13. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    RTI20171013_zaa_n230_019.jpg
  • June 17, 2017 - Rome, Italy - CGIL, Italian trade union, calls for a demonstration to protest against the reintroduction of a new type of work 'voucher' system, coupons to pay jobs for less, that were abolished last March with an amendment of the Government in Rome, Italy on June 17, 2017. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    20170617_zaa_n230_153.jpg
  • October 22, 2016 - Rome, Italy - Thousands of people shout slogans and wave flags as they take to the streets to protest Prime Minister Matteo Renzi's government politics and to say 'NO' at the upcoming constitutional referendum in Rome, Italy, on 22 October 2016. (Credit Image: © Giuseppe Ciccia/NurPhoto via ZUMA Press)
    20161022_zaa_n230_113.JPG
  • File photo of Kim Kardashian and Kanye West head for lunch at the trendy restaurant LÂ’Avenue in Paris, France, May 19, 2014. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_025.jpg
  • File photo of Kim Kardashian and Kanye West attending the Vanity Fair Oscar party at Wallis Annenberg Center for the Performing Arts on February 09, 2020 in Beverly Hills, Los Angeles, CA, USA. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by David Niviere/ABACAPRESS.COM
    737195_022.jpg
  • File photo of Kim Kardashian and Kanye West attend the Manus x Machina: Fashion in an Age of Technology Costume Institute Benefit Gala at Metropolitan Museum of Art on May 2, 2016 in New York City, NY, USA. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Lionel Hahn/ABACAPRESS.COM
    737195_015.jpg
  • File photo of File : File photo : Kanye West and Kim Kardashian attend the 57th Annual Grammy Awards at the Staples Center in Los Angeles, CA, USA, on February 8, 2015. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Lionel Hahn/ABACAPRESS.COM
    737195_014.jpg
  • File photo of Kanye West and Kim Kardashian attend the RocNation Pre-Grammy Brunch in Beverly Hills, Los Angeles, CA, USA on February 7 2015. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Lionel Hahn/ABACAPRESS.COM
    737195_013.jpg
  • File photo of Kanye West and Kim Kardashian attend the 2014 LACMA Art + Film Gala honoring Barbara Kruger and Quentin Tarantino presented by Gucci at LACMA in Los Angeles, CA, USA, on November 1, 2014. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Lionel Hahn/ABACAPRESS.COM
    737195_012.jpg
  • File photo of Artist Kanye West looks on in the Oval Office of the White House during a meeting with President Trump to discuss criminal justice system and prison reform on October 11, 2018 in Washington, DC. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Olivier Douliery/ Abaca Press
    737195_008.jpg
  • File photo of Artist Kanye West looks on in the Oval Office of the White House during a meeting with President Trump to discuss criminal justice system and prison reform on October 11, 2018 in Washington, DC. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Olivier Douliery/ Abaca Press
    737195_007.jpg
  • File photo of Kim Kardashian and Kanye West attend BET Honors red carpet at the Warner Theatre on January 24, 2015 in Washington, DC, USA. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Olivier Douliery/ABACAPRESS.COM
    737195_006.jpg
  • File photo of Kim Kardashian and Kanye West are spotted leaving Balmain Office and Kim arriving at Hotel Royal Monceau in Paris, France on September 24, 2014. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_028.jpg
  • File photo of Kim Kardashian and Kanye West arrive at their hotel in Paris, France on June 17, 2012. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_023.jpg
  • File photo of Kayne West attending Balmain's Spring-Summer 2015 Ready-To-Wear collection show held at the Palais de Tokyo in Paris, France, on September 25, 2014. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Alban Wyters/ABACAPRESS.COM
    737195_020.jpg
  • File photo of Kanye West and Kim Kardashian attending the Louis Vuitton Menswear Spring Summer 2019 show as part of Paris Fashion Week in Paris, France on June 21, 2018. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Aurore Marechal/ABACAPRESS.COM
    737195_019.jpg
  • File photo of Kim Kardashian and Kanye West attend the Manus x Machina: Fashion in an Age of Technology Costume Institute Benefit Gala at Metropolitan Museum of Art on May 2, 2016 in New York City, NY, USA. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Lionel Hahn/ABACAPRESS.COM
    737195_016.jpg
  • File photo of File photo dated October 2, 2012 of Kanye West attending the Chanel spring-summer 2013 collection held at the Grand Palais as part of the Paris Fashion Week in Paris, France. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_010.jpg
  • File photo of Kim Kardashian and Kanye West backstage of Stephane Rolland Fall-Winter 2012-2013 Haute Couture collection show during Haute-Couture Fashion Week held at the Cite de lÂ’Architecture in Paris, France, on July 3, 2012. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Nicolas Briquet/ABACAPRESS.COM
    737195_004.jpg
  • File photo of Kim Kardashian and Kanye West backstage of Stephane Rolland Fall-Winter 2012-2013 Haute Couture collection show during Haute-Couture Fashion Week held at the Cite de lÂ’Architecture in Paris, France, on July 3, 2012. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Nicolas Briquet/ABACAPRESS.COM
    737195_003.jpg
  • File photo of Kim Kardashian and husband Kanye West are seen at L'Avenue restaurant where they had lunch with Kris Jenner and Kendall Jenner during the Paris Fashion Week, in Paris, France on September 25, 2014. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_029.jpg
  • File photo of Kim Kardashian and Kanye West leaving Royal Monceau palace hotel in Paris, France on September 24, 2014. The parisian fashion week starts today and runs until Oct. 2. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_027.jpg
  • File photo of Kim Kardashian, Kanye West, their baby baby North and Kris Jenner are spotted leaving their apartment in Paris, France on May 23, 2314. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_026.jpg
  • File photo of KIm Kardashian and Kanye West out in Paris, France, during Haute-Couture Fashion Week, on July 03, 2012. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by ABACAPRESS.COM
    737195_024.jpg
  • File photo of street style, Kanye West arriving at Dries Van Noten Ready-to-Wear Spring-Summer 2015 show held at Grand Palais, Paris, France on september 24th 2014. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Sophie Mhabille/ABACAPRESS.COM
    737195_021.jpg
  • File photo of Kanye West and Kim Kardashian attending the Louis Vuitton Menswear Spring Summer 2019 show as part of Paris Fashion Week in Paris, France on June 21, 2018. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Aurore Marechal/ABACAPRESS.COM
    737195_018.jpg
  • File photo of Kanye West attending the Vogue 95th anniversary party held in Paris on october 03, 2015. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Aurore Marechal/ABACAPRESS.COM
    737195_017.jpg
  • File photo of Kim Kardashian and Kanye West front row at the Givenchy Fall-Winter 2013/2014 Ready-To-Wear collection show held at the Halle Fressinet, in Paris, France on March 3, 2013. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Thierry Orban/ABACAPRESS.COM
    737195_011.jpg
  • File photo of Artist Kanye West speaks in the Oval Office of the White House during a meeting with President Trump to discuss criminal justice system and prison reform on October 11, 2018 in Washington, DC. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Olivier Douliery/ Abaca Press
    737195_009.jpg
  • File photo of Kanye West attending Maison Martin Margiela's Fall-Winter 2014/2015 Ready-To-Wear collection show held at Salomon de Rothschild Hotel in Paris, France on February 28, 2014. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Aurore Marechal/ABACAPRESS.COM
    737195_005.jpg
  • File photo of Kim Kardashian and Kanye West attending the Valentino Haute-Couture Show as part of Paris Fashion Week Fall-Winter 2012-2013 held at the Hotel Salomon de Rothschild in Paris, France on July 4, 2012. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Christophe Guibbaud/ABACAPRESS.COM
    737195_002.jpg
  • File photo of Kanye West and Kim Kardashian with Balenciaga bag leaving Kanye West Sunday service at Des Bouffes du Nord Theater during Women fashion week Fall/Winter 2020-2021 in Paris on March 01, 2020. Kim Kardashian West spoke out about Kanye West's bipolar disorder Wednesday, three days after the rapper delivered a lengthy monologue at a campaign event touching on topics from abortion to Harriet Tubman, and after he said he has been trying to divorce her.Kardashian West said in a statement posted in an Instagram Story that she has never spoken publicly about how West's bipolar disorder has affected their family because she is very protective of their children and her husband's "right to privacy when it comes to his health." Photo by Nasser Berzane/ABACAPRESS.COM
    737195_001.jpg
  • June 24, 2017 - London, England, United Kingdom - EDL leader IAN CROSSLAND argues with an anti fascist on Whitehall. The English Defence League (EDL) held a March on Parliament, from Charing Cross to Victoria Embankment, opposed by a counter demonstration by Unite Against Fascism. Scotland Yard said it was using public order laws to restrict the marches 'due to concerns of serious public disorder, and disruption to the community' following terrorist attacks in Manchester, Westminster and Finsbury Park. (Credit Image: © Joel Goodman/London News Pictures via ZUMA Wire)
    RTI20170624_zaf_l94_043.jpg
  • RELEASE DATE: January 22, 2010<br />
MOVIE TITLE: Extraordinary Measures<br />
STUDIO: CBS Films<br />
DIRECTOR: Tom Vaughan <br />
PLOT: A drama centered on the efforts of John and Aileen Crowley to find a researcher who might have a cure for their two children's rare genetic disorder<br />
PICTURED: BRENDAN FRASER as John Crowley and HARRISON FORD as Dr. Robert Stonehill <br />
(Credit Image: © CBS Films/Entertainment Pictures/ZUMAPRESS.com)
    20100122_rrb_g90_057rti.jpg
  • June 24, 2017 - London, Greater London, UK - London, UK. Ian Crossland at the demo.  The English Defence League ( EDL ) hold a March on Parliament , from Charing Cross to Victoria Embankment , opposed by a counter demonstration by Unite Against Fascism . Scotland Yard said it was using public order laws to restrict the marches ''due to concerns of serious public disorder, and disruption to the community'' following terrorist attacks in Manchester , Westminster and Finsbury Park and the Grenfell Tower fire  (Credit Image: © Joel Goodman/London News Pictures via ZUMA Wire)
    20170624_zaf_l94_004.jpg
  • June 24, 2017 - London, UK - London, UK. 24th September 2017.  Supporters pose with wreaths on London Bridge after the march by well over a thousand supporters of the recently formed Football Lads Alliance marched to the centre of London Bridge to protest what they see as the UK government's reluctance in tackling the current extremism problem. They marched in silence and without banners, posters or placards to a short rally and moment of silence. Police had imposed conditions on the event under Section 12 and 14 of the Public Order Act, 1986, due to concerns of serious public disorder, and disruption to the community, which prevented them from marching to Borough Market.  Peter Marshall ImagesLive (Credit Image: © Peter Marshall/ImagesLive via ZUMA Wire)
    20170624_zap_d99_041.jpg
  • June 24, 2017 - London, United Kingdom -  Supporters pose with wreaths on London Bridge after the march by well over a thousand supporters of the recently formed Football Lads Alliance marched to the centre of London Bridge to protest what they see as the UK government's reluctance in tackling the current extremism problem. They marched in silence and without banners, posters or placards to a short rally and moment of silence. Police had imposed conditions on the event under Section 12 and 14 of the Public Order Act, 1986, due to concerns of serious public disorder, and disruption to the community, which prevented them from marching to Borough Market.  Peter Marshall ImagesLive (Credit Image: © Peter Marshall/ImagesLive via ZUMA Wire)
    20170624_zap_d99_041.jpg
  • Story of the Week : Launched Wednesday May 1, 2019 on www.zReportage.com Story #701: AGORAPHOBIC Buster. Some people stop going into situations because of a fear of being overwhelmed by anxiety and not being able to escape or get help. Buster Burns, a former drag queen, has 8 personalities and has not left his house for the past 9 years. Buster suffers from agoraphobia. 'Facebook is my whole life,' he stated of the social media platform, which allows him to interact with others without leaving the security of his home. Those who suffer from this debilitating disorder typically avoid places where they feel immediate escape might be difficult, such as shopping malls, public transportation, and open places. Agoraphobia is particularly common in people with panic disorders. Their world may become smaller as they are constantly on guard, waiting for the next panic attack. Buster Burns lives in Little Rock, Arkansas and used to be as extroverted as they come, once a successful drag queen, he would walk the stage as Ophelia every week in a crowded club. After the sudden death of a friend in 2000, Buster started slowly to retreat from public life. Today Buster spends his days with a supportive Facebook community, chatting for up to 10 hours a day. His sister visits him once a week to bring groceries and anything he might need from the outside world. Agoraphobia currently affects over 200,000 people in the United States. This debilitating condition is chronic, and those affected are often unable to leave their house because they need to avoid people and places that cause anxiety. (Credit Image: ? David Tesinsky/ZUMA Wire)
    20190501_701_t127_011.jpg
  • June 8, 2017 - Inconnu, inconnu - 07/06/2017 - A patch could help improve sleep and even save lives by detecting a sleep disorder that usually requires hospital Sleep apnea is a serious condition that happens when a person’s breathing in interrupted during sleep.Left untreated it sufferers stop breathing repeatedly , sometimes hundreds of times a night.This means the brain and the rest of the body may not get enough oxygen.It can lead to high blood pressure, a stroke, heart attack, diabetes depression and headaches.People who are suspected of having the condition are often sent for a sleep study known as polysomnography.This involves their spending the night sleeping at a clinic, with numerous electrodes hard-wired to their head. The new SomnaPatch is simple and – according to the recently-released results of a study – almost as accurate.Made by California-based Somnarus, the SomnaPatch weighs less than 28 grams / one ounce.It consists of a forehead-worn disposable adhesive patch connected to a nosepiece. It is worn while the patient sleeps in their own bed, and uses integrated sensors to measure and record factors such as nasal pressure, blood oxygen saturation, heart rate, respiratory effort, sleep duration and changes in body position.As part of its efforts to obtain US Food and Drug Administration approval, Somnarus conducted a study of the device at three US sleep clinics last year. This involved having 174 test subjects undergo standard polysomnography while also using the SomnaPatch.When the readings obtained by the two approaches were compared, they were found to be in agreement 87.4 percent of the time.Additionally, a separate home usability study found that 38 out of 39 users were able to use the device to record at least four hours of sleep, guided by nothing but the included instructions.A spokesman said:’ SomnaPatch records respiratory patterns, pulse oximetry data and estimates sleep time based on proprietary algorithms and
    20170608_zaf_v01_254.jpg
  • May 4, 2019 - Paris, France - Hundreds of officers oversee the protest to prevent disorder during the Yellow Vest protest on May 4, 2019 in Paris, France. Act 25 of the Gilets Jaunes (Yellow Vests) protests in Paris against the economic reforms of President Macron saw thousands of people march through Paris wearing the high vis vests associated with the protests. (Credit Image: © Guillaume Pinon/NurPhoto via ZUMA Press)
    20190504_zaa_n230_820.jpg
  • September 5, 2017 - Shenyang, Shenyang, China - Shenyang, CHINA-5th September 2017: (EDITORIAL USE ONLY. CHINA OUT) ..Nick Vujicic gives a speech at Shenyang University in Shenyang, northeast China's Liaoning Province, September 5th, 2017. Nicholas James Vujicic is an Australian motivational speaker born with tetra-amelia syndrome, a rare disorder characterized by the absence of arms and legs. (Credit Image: © SIPA Asia via ZUMA Wire)
    RTI20170905_zaa_s145_177.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_008.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_009.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_005.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_006.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_003.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_001.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_010.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_011.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_002.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_004.jpg
Next