A MUM battling against a debilitating disease wants a lifeline drug prescribed by health chiefs.

Multiple sclerosis (MS) sufferer Judith Andrews, of Vernon Grove, Droitwich, has received daily Copaxone injections for four years.

She was diagnosed with the condition in 1989 after suddenly losing the sight in her left eye.

MS attacks the central nervous system and it forced Judith to have regular hospital treatment. She also needed a wheelchair and constant rest.

In 1997 her life took an exciting turn when she was asked to participate in trials for a new MS treatment - Copaxone.

The 39-year-old said: "I haven't looked back since taking this miracle drug. It's given me a new lease of life and all the energy I need to play with my three lively children."

The trials are now ending. In the short-term, the drug company which makes Copaxone is continuing to provide Judith with her daily dose but she must seek long-term funding. A year's supply costs £6,500.

She has called on Worcestershire Health Authority to prescribe the therapy but it has refused.

Judith said: "Life without Copaxone frightens me. I know how much good it has done me and my family and I'm scared about facing a future without it."

A health authority spokeswoman said: "We have a policy that applies to patients coming off drug trials.

"In general we do not fund ongoing treatment costs once a trial has finished."

She added that in Judith's case, the trial results are due to be analysed to determine what the benefits of the treatment are before a decision to commit public funds is made.