[SallyC]

When the MS society gives money for drug companies to research a new drug for MS and that drug is approved, shouldn't we get credit for that?

In other words, should PwMS, using a drug, get credit for the moneys NMSS put into that drug? Our cost should reflect that, IMHO.

Of course it could be quid pro quo and the drug Cos probably donate to NMSS, so they will favor the drug and then the FDA approves it. Like I say what a racket!!