CANADA-FRANCE-IMMIGRATION-CHILDREN-HEALTH-RESEARCH
Julien Ferrer prepares a syringe with the treatment for his genetic disorder hypophosphatasia in Winnipeg, Canada, on May 17, 2018. - Born in France, Ferrer's family moved to Winnipeg to experiment with a cure for hypophosphatasia. At birth, doctors gave Julien Ferrer only a slim chance of surviving a rare childhood bone disease. Fifteen years on, the French teen is living a normal life in Canada, where he received cutting-edge treatment -- and new hope for the future. (Photo by Clément SABOURIN / AFP) (Photo credit should read CLEMENT SABOURIN/AFP via Getty Images)
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Contact your local office for all commercial or promotional uses. Full editorial rights UK, US, Ireland, Italy, Spain, Canada (not Quebec). Restricted editorial rights elsewhere, please call local office.TO GO WITH AFP STORY BY CLEMENT SABOURIN
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972980260
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AFP
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17 May, 2018
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AFP
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