2016 archive
ITV coverage - "Parents of terminally ill toddler fundraise for cure"
June 07, 2016
"The family of a little girl from Chorley with an extremely rare life-limiting genetic illness are raising money to fund a doctor to research treatments.
Three year old Bella Morris suffers from a condition called 'Vanishing White Matter' which causes sufferers to lose their ability to eat, walk, see and hear. It's very rare and affects just 1 in 40 million people. Currently there is no cure..."
Chorley Guardian - "Parents of terminally ill Chorley toddler plea to raise cash for doctor"
May 30, 2016
"Bella Morris aged 3 from Chorley is suffering from a rare life-limiting illness called Vanishing White Matter. The family are campaigning to raise money to fund a doctor who is researching treatments for the illness... Picture by Paul Heyes, Thursday May 26, 2016."
Blackpool Teaching Hospitals - "Heart-broken dad fights to save his daughter"
June 21, 2016
"When Peter Morris was told his two-year-old daughter Bella had an incurable condition his world crumbled.
“I just wished it was me and not Bella,” said Peter.
Bella, who is now three years old, has a life-limiting condition called ‘Vanishing White Matter’ which affects less than 200 children across the world..."