It is really nice that there’s a committee in place, but that doesn’t do much for the family that has a family member who is suffering from MS. This drug is a well known drug that demonstrates progress and promise when you have this disease. As I’m sure most people know, this is quite a debilitating disease. There is only one direction it goes. When we have a drug that shows promise, I think we should be latching on to it.
I guess my real question really comes down to how we get access to this. I have a letter here from the Minister. My original question was: is this covered? The Minister’s letter comes back saying all you have to do is ask for it to get it approved. What more do we need to do?