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 suffer from Hutchinson-Gilford progeria syndrome (HGPS).


Ashanti Elliot Smith, seen here with her mum, Phoebe, is one of two people in Britain who suffer from Hutchinson-Gilford progeria syndrome (HGPS) .


The genetic condition has left her with the body of a pensioner, and she is not expected to live past the age of 15.


SWNS.com Tony Kershaw


A side effect of HGPS is alopecia.


A side effect of HGPS 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 was furious.


Her mother was furious.


Phoebe told their 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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