MS symptoms

[heathers]

So I had a neurologist appointment on Tuesday. To update you, I started on Copaxone in August 2014. It's a daily injection that Nic performs for me each morning. It leaves me sore with needle marks and welts that last up to 3 weeks sometimes. Sometimes it hurts to even get hugs from people. Boo hoo, right? The idea is that the medication is

Comments

[rebism]

Man, that sounds like a lot to cope with. Again I say you're doing amazingly to be adapting to all that. And Nic sounds amazing too.

It sucks that invisible symptoms don't get sympathy. It's so rude of people to assume that if they can't see it, you're making it up, or it's not really that bad.

*hugs*