Thursday, October 30, 2014

A School Ordered This Terminally-Ill Girl To Remove Her Favourite Wig And Left Her In Tears

Ashanti Elliot Smith is not expected to live past the age of 15.


Ashanti Elliot Smith, seen here with her mum Phoebe, is one of two people in Britain who suffers from Hutchinson Gilford Progeria.


Ashanti Elliot Smith, seen here with her mum Phoebe, is one of two people in Britain who suffers from Hutchinson Gilford Progeria .


The disease has left her with the body of a pensioner: she is not expected to live past the age of 15.


SWNS.com Tony Kershaw


A side-effect of the disease is alopecia.


A side-effect of the disease is alopecia.


SWNS.com Tony Kershaw


To disguise it, she wears her favourite pink wig. But when she wore it to school, a teacher told her to remove it.


To disguise it, she wears her favourite pink wig. But when she wore it to school, a teacher told her to remove it.


She was told it might encourage other pupils at Oakmeeds Community College, in Burgess Hill, West Sussex, to dye their hair.


SWNS.com Tony Kershaw


Her mother Phoebe was furious.


Her mother Phoebe was furious.


She told her local paper, The Argus , that the family could not afford human hair wigs and were donated the bright pink one by friends of the family.


SWNS.com / Tony Kershaw




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