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DUKAS_189994162_NUR
Mexico’s President Claudia Sheinbaum News Conference
Mexico's President Claudia Sheinbaum speaks during a news conference at the national palace about the progress on emergency response in the five affected states: Puebla, San Luis Potosi, Veracruz, Queretaro, and Hidalgo, due to flooding in Mexico City, Mexico, on October 15, 2025. (Photo by Carlos Santiago/Grupo Eyepix/NurPhoto) -
DUKAS_189941902_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
Bottles of water are received at a collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding. This center is installed next to the National Autonomous University of Mexico (UNAM) Olympic Stadium in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941901_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
Various products are received at a collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding. The center is installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM) in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941900_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
A person receives products to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding at a collection center installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM), in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941899_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
A person receives products to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding at a collection center installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM), in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941898_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
A collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding is installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM) in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941910_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
Various products are received at a collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding. The center is installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM) in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941909_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
Various products are received at a collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding. The center is installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM) in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941908_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
A person receives products to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding at a collection center installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM), in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941906_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
People come to take various items to a collection center to support the communities in Hidalgo, Puebla, and Veracruz affected by the recent floods. The center is installed next to the Olympic University Stadium of the National Autonomous University of Mexico (UNAM) in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941905_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
A collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding is installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM) in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941904_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
Bottles of water are received at a collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding. This center is installed next to the National Autonomous University of Mexico (UNAM) Olympic Stadium in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941903_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
A person receives products to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding at a collection center installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM), in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189941897_NUR
Collection Center For States Affected By Flooding At The National Autonomous University Of Mexico (UNAM) In Mexico City
Various products are received at a collection center to support communities in Hidalgo, Puebla, and Veracruz affected by recent flooding. The center is installed next to the Olympic Stadium of the National Autonomous University of Mexico (UNAM) in Mexico City, Mexico, on October 13, 2025. (Photo by Jose Luis Torales/NurPhoto) -
DUKAS_189875095_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875094_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875093_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
Transporters are present during a total closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875092_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
National Guard members are present after the complete closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875091_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875090_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
Transporters are present during a total closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875088_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875087_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875086_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
Transporters are present during a total closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875085_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
National Guard members are present after the complete closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875084_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
An ambulance is visible after the complete closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875083_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
People walk after the complete closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875082_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875081_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875080_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
Transporters are present during a total closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875079_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
A dog is present after the complete closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875078_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
The Mexico-Puebla highway in Santa Rita Tlahuapan is completely closed due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway on October 11, 2025. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875077_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
Transporters are present during a total closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875076_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
People walk after the complete closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_189875075_NUR
Gas Tanker Accident Causes Total Closure Of The Mexico-Puebla Highway
People walk after the complete closure of the Mexico-Puebla highway in Santa Rita Tlahuapan, Mexico, on October 11, 2025, due to an accident involving a gas tanker headed toward Mexico City, which overturns and subsequently explodes at kilometer 72 of the highway. (Photo by Gerardo Vieyra/NurPhoto) -
DUKAS_188390459_NUR
National Public Security Council Meeting
Governor of Nuevo Leon Samuel Garcia and Governor of Puebla Alejandro Armenta Mier participate in the 51st Ordinary Session of the National Public Security Council, where the security cabinet and the governors of the 32 states participate, at the National Palace in Mexico City, Mexico, on September 2, 2025. (Photo by Carlos Santiago/Eyepix Group/NurPhoto) -
DUKAS_188175451_ZUM
Relic Of Saint Jude Thaddeus Leaves Mexico
August 28, 2025, Mexico, Cdmx, Mexico: Hundreds of parishioners arrive at the Metropolitan Cathedral of Mexico City to bid farewell to the Relic of Saint Jude Thaddeus. This relic is a bone from his arm. They arrived on July 29, 2024, and will return to Rome in December after another tour of the places they visited initially, which are the State of Mexico, Tlaxcala, and Puebla. (Credit Image: © Josue Perez/ZUMA Press Wire (FOTO: DUKAS/ZUMA)
Represented by ZUMA Press, Inc. -
DUK10075194_123
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge drinks a Coca-Cola at a Sunday lunch at his family’s home in Puebla, Mexico on April 23, 2017. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He is now part of a sports team for people with disabilities. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272620
(c) Dukas -
DUK10075194_122
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge plays bocce ball in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272556
(c) Dukas -
DUK10075194_121
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge walks on a track with his team in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272537
(c) Dukas -
DUK10075194_120
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge does stretches with his mother in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272539
(c) Dukas -
DUK10075194_119
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge works on a crossword with his sister-in-law at his home in Puebla, Mexico on April 23, 2017. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He is now part of a sports team for people with disabilities. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272632
(c) Dukas -
DUK10075194_118
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge injects himself with insulin during a Sunday lunch at his family’s home in Puebla, Mexico on April 23, 2017. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He is now part of a sports team for people with disabilities. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272629
(c) Dukas -
DUK10075194_117
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge works on a puzzle during a Sunday lunch at his family’s home in Puebla, Mexico on April 23, 2017. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He is now part of a sports team for people with disabilities. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272611
(c) Dukas -
DUK10075194_116
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge eats yogurt as he peels carrots for lunch at his home in Puebla, Mexico on April 23, 2017. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He is now part of a sports team for people with disabilities. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272590
(c) Dukas -
DUK10075194_115
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge looks at a plastic container of carrots at his home in Puebla, Mexico on April 23, 2017. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He is now part of a sports team for people with disabilities. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272583
(c) Dukas -
DUK10075194_114
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge displays his swimming medals in his bedroom in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272597
(c) Dukas -
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REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge walks on a track with his team in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272538
(c) Dukas -
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REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge displays his swimming medals in his bedroom in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272604
(c) Dukas -
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REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge plays bocce ball in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272560
(c) Dukas -
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REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Jorge displays his swimming medals in his bedroom in Puebla, Mexico on April 23, 2017. He is part of a sports team for people with disabilities. Jorge Antonio Moreno Gaytán, a 34-year-old Mexican man, lives with his parents in Puebla, Mexico. He was diagnosed with Prader-Willi syndrome at age seven. He weighs 136 kilos (300 pounds) and stands 152 centimeters (4 feet 12 inches). Jorge is in the process of getting bariatric surgery. As a teenager, he would pawn his siblings’ belongings in order to have money to buy food. He was also known to leave restaurants without paying. “Our worst enemy is hunger, it’s what will kill us”, Jorge says. He has been in a relationship for 11 years with, Maria Guadalupe Pilar Saucedo Granda, known as “Lupita’, also diagnosed with Prader-Willi syndrome. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272600
(c) Dukas -
