Fear mongering is the basis for recommendation of Interferons and Copaxone. There is probably a component of the "MS" syndrome which involves immune cells. We say we don't know what causes that, or many other aspects of the syndrome, like heat sensitivity. But up until Copaxone there was *no* *treatment*. If you don't take so-called DMDs, you are to believe there is, still, in 2013, *no* *treatment*. That is simply not true.
There is a definite self-interest involved in prescribing drugs which costs $30,000 per patient per year and at the same time, are "not associated with a reduction in progression of disability." In other words, they don't prevent it; they don't even slow it down
The self-interest is shared in unequal amounts by everyone except the patient: profit. MS neurologists have been said to take kickbacks/bribes for prescribing expensive "MS" drugs, with tens of millions paid to keep it quiet. The same biases against the less expensive PTA treatment are shared by lobbyist, advisers, and executives of public and private insurance companies. It is not hard to imagine them being "on the take" too.
One is forced to estimate the cost to insurance companies based on 50% of patients, because no one can justify costs
twice the current amount. So after overnight "conversion" to "Secondary Progressive" these "DMDs" mysteriously become useless, losing all their efficacy at once. At which point we are definitely back to 1970s treatments: none.
That justifies the experimentation and randomized trials on the hopeless sufferers. At least, as human beings, we should allow them to pay for CCSVI treatment
in Canada, by ethical professionals, and not force them to travel outside the country or be satisfied with the alternative, which is slow progression, increasing disability, and early death.