Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I never found away around receiving the shot until I stopped all together.
To quote my (older) sister: "Shut up and man up. This is not going to kill you."
She was right.
I think self injecting for me hasn't been so bad because I was dx'd as a type 1, insulin dependent, diabetic back in 1981. I've been giving myself up to four shots a day for that, so self injecting the Avonex was not that big a deal. Still, I hate feeling spent every Tuesday. I don't know that I'll ever get used to that but then, taking the Avonex appears to be worth it as I haven't had a relapse in almost four years.
The Copaxone shots are real small and non-invasive compared to some of the other therapy shots. Might you think about a change? Giving yourself one shot before going to bed would be just like someone living with Type 1 diabetes?
I cannot comment on the "man up" comment because I don't understand that naturally because I'm a woman. What I do understand is taking medication making you sick is just plain torture. Hopefully you will make it to the 4 month marker and the fevers will go away. I only hope that you you.
I say all this to encourage you to continue, if you feel it's right for you. The side effects are a nuisance, but I have faith that taking the medication now will pay off later. It gets me through...