switching from copaxone to avonex
 

I was taking copaxone but having bad site reactions & it really didn't seem to be helping me any so my neuro wants me to start avonex, (I'm waiting on the nurse to call so that she can come out and teach me, though it might be next week sometime)

The thought of the needle and no auto injector really has me stressing out, not to mention the flu like syptoms that it could cause. Am I worrying too much? What can I expect? Ohhhhhhh I hate needles and I hate this freakin' disease!

I have done Beta, and got kicked over to Copaxone. I have never taken Avonex, so I cant help you there, but I did want to step forward, and offer up a hug. :hug:

Changing to any new drug is so stressful. hang in there.

you will feel flu-like: sore muscles, warm, achy for about a day afterward. using the injections are okay once you get used to it. if it is troublesome, then get your doc to write you a script for smaller 25gauge needles. and at least it's only once a week!

It was the other way around for me, Suz. I left Avonex because of the side effects and went to Copaxone. I had no site reactions to it, but had too many exacerbations, so now I'm on LDN..:D

Not all PwMS have the major flu sx with Avonex, as I had, so Good luck.:hug:

Hi,
I did Avonex before Copaxone. I found it is best to start with 1/4 of the dosage, if your Neuro permits. Then go to 1/2 a dosage, when ready. Then up to full dosage.

This way you see how your body tolerates it. Some people don't get the flu, some pre-medicate, or medicate every few hours. Maybe pick a day of the week when you will be staying at home, so you can treat any symptoms you get, if any.

The needle is intimidating, but truthfully, injecting into the muscle, never gave me a skin reaction. I learned to dart it in, if that helps you. Count to three, and just do it. It is over quickly. :)

It didn't agree with me, but so many people have no problems with Avonex. I hope you are one of them, and that it helps you. Good Luck.:)