LITTLE Enola Halleron needs your help to get the vital drugs she needs to prolong her life.

Today the Lancashire Telegraph has launched a petition calling on health secretary Jeremy Hunt to act urgently after health bosses again delayed their decision until later this year, a move branded a “potential death sentence” for the 11-year-old.

Enola, who will never grow more than one metre tall, suffers from the super rare mucopolysaccharidosis (MPS), which causes heart disease, skeletal abnormalities, vision and hearing loss, and difficulty breathing.

She has now gone almost a month without Vimizim following several years participation in a clinical trial, and will now be the subject of a harrowing video diary capturing her deterioration.

Her family believes the drug could add 10 years to Enola’s life expectancy of around 25.

So we are trying to collect as many signatures as possible to help the Halleron family persuade Mr Hunt to immediately make funds available for the supply of Vimizim for free on the NHS.

So come on East Lancashire lets stand together and help little Enola get the treatment she deserves.