Oh, those IPIRs are terrible. Some people have the one, while others just keep having them. I took Copaxone for three years, and had about six. I finally stopped, not because of the IPIR, but because it turned into an allergic reaction. Fortunately it was slight.
Personally if I were you I'd keep an Epi-pen in the house. This is a great thing to have even if you don't have serious allergies. If you have the IPIR again, stay awake until the IPIR has passed. My allergic reaction was extreme skin itching, and slight swelling of the face.
What the Copaxone people will tell you is that you injected in an area that didn't have enough fat. That's more or less true, but it's oversimplified. Copaxone causes areas of scar tissue, especially if you don't massage the area or heat it after injection. I had a lot of lipoatrophy, and areas would become 'uninjectable' because I wasn't treating my injection sites very well. So after a while, the safe areas for injections became too scarred for me to continue.
HI, the reaction you had is considered a side effect of Copaxone and as long as it dissipates within 15 or 20 minutes there is no need to worry.
Several members on here have experienced this reaction. Hopefully they will pop up and share their experiences with this. I know Jensequitur and HVAC have both experienced this.
You were right in calling the nurse for advice.
Ren
Men sometimes are totally dense aren't they? LOL!
I'm glad the SS nurse spoke with you today and unfortunately, you were in the 16% huh? Don't we always find a way to sneak into those small percentiles!
Perhaps it was a defense mechanism, perhaps he is totally oblivious, but whatever the case, you need to speak to him and let him know that there can be a reaction and your body has decided that one time to do so and it was "no joke". Tell him the next time you say you're having a problem, to take it serious. Sheesh! My bf is just "dense" as the rainforest in the Amazon! Heh.
Hugs to you and lets pray that this doesn't happen again!
Lisa
It was very scarry! I talked to my SS nurse today and she said about 16% of people have that reaction from time to time. What made it worse is that my husband didn't seem to be worried. Guess he thought I was joking...not too sure why I'd joke like that.
He still hasn't said anything about it...weird. His mom says it's his defense mechanism...that's a strange one if you ask me! He always takes that kind of stuff seriously. Praying it doesn't happen again. Although it turned out okay, it still makes me nervous!
I think Kelly has had that happen to her too. Sorry to hear that -- it must of been really scarey!
I'm glad your shot last night went well! Phew! I can't imagine the anxiety building up as you prepare the injection site and pray to the Copaxone Gods "please please not again!".
Hugs to you!
Lisa
I've had this happen before after the shot. This can happen with Copaxone, and it did during the first year I was on the medicine. One, like the one you had, was more apparent than the other reactions. I told my neurologist, and he thinks I was injecting in my blood stream. He gave me some tips to avoid doing that again, and for the life of me can't remember what they were. Maybe someone on the forum does know.
I think I had two or maybe three reactions like that in my first year on Copaxone, and have not had any problems at all since.