November 25, 2016

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

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!

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..."

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."
 

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..."