2016 archive


November 25, 2016

After a lot of forms, papers and documents had been cleared we have now achieved registered charity status!

Take A Break - Bella's big brother fundraises for cure "Brotherly Love"

November 17, 2016

Leo Brindle, Bella's eldest brother decided to take it upon himself to raise funds to help find a cure to save his sister and fight this awful disease. We couldn't be prouder of him!

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..."

Please reload