An Indian teenager suffering from a rare genetic disease faces deportation after her appeal to stay in Britain for the treatment was rejected.
Zarine (15), a student of the South Camden Community School, is currently being treated at the Great Ormond Street Hospital. Doctors, local lawmaker, teachers and others have been supporting a campaign to allow her to stay in the UK.
Zarine came to the UK in 2004 with her mother Tasnim as visitors. She was later diagnosed with the bone marrow disease Fanconi-Bickel Syndrome (FBS), of which doctors say there are only 112 other cases in medical history.
Refusing her appeal to stay in the UK, immigration judge Justice Herlihy said here last week that she had "enormous sympathy for Zarine, but was not satisfied that Zarine's symptoms cannot be treated in India".
Though 2000 people have signed a petition to make her stay in UK but this not good, the petition has been organized by some "Rentia Family Anti-Dpoeration Campaign Group" so its clear that its not normal people and its also clear that they are always willing to deport otherwise how come such group came in existense if there is no regular and unlogistic deportation.
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