Bit stiff and achey this morning - think it’s the onset of Autumn - but otherwise OK.
I’ve had numbness on my face once (before I was diagnosed), but it was so very slight I wasn’t even sure, and thought I might be imagining things. It can be literally anywhere; it just depends where the lesions form.
On the bright side, as it’s unlikely to be a reaction to Copaxone, it won’t mean you need to quit that. You maybe need to report it to doctor or MS nurse as a “minor” relapse, but it’s unlikely to affect any treatment decisions, as the Copaxone wouldn’t have had time to work yet anyway. So it’s not evidence it’s not working.