Millions wasted by NHS on expensive, useless MS drugs

See report in the Telegraph, where you will read that experts "called for a Government-backed scheme to provide the drugs to be scrapped and called for a public inquiry. In total at least £250 million could have been saved if a review had been carried out on the “costly failure” after its first two years, they warn."And also "The four drugs involved Avonex, Betaferon, Copaxone and Rebif, cost around £8,000 per patient per year."

These expensive drugs have been provided on the NHS for six years now, during which time they have performed less well than a placebo. - Why then, has it taken till now for anyone to seek to do anything about this? MS sufferers have enough to contend with, without being given false hope and useless drugs. And why can't the many legal eagles on the State payroll devise watertight contracts to ensure that the drug companies do not screw the NHS for costly drugs that prove to be worthless?

It is time we had some people in Government and in the Dept of Health with enough sense to resist the blandishments and lies of the pharmaceutical companies, and enough courage and integrity to listen to the people who are ill, rather than to the drug company executives who cosy up to the people in power, seeking to make money out of their expensive products, regardless of how useless or harmful those products are. During those six years of uselessness, why was no-one taking heed of their uselessness to patients? - No-one listening to the patients?