Hello everyone!

This may be opening a can of worms, but I just wondered if anyone else ever got
the feeling that their medicine was hurting more than helping? When I take my
medicine (which I do 99% of the time); I feel more sluggish, less sharp
mentally, and border-line depressed. I'm in the process of changing jobs since
I moved, so that means changing insurance which will mean a new neurologist ...
which may mean new medicine - but just wanted other opinions while I finish my
supply of Copaxone. I haven't had any problems taking it, or any attacks since
I've been on it - so it may be that I am just tired of being one of the many
guinea pigs testing the different types of MS medicine.

Just some thoughts,
Toni