28th February 2008
Well, I know I kept everyone updated about changing off the betaseron onto the steroids and then a few weeks ago on to copaxone. I had posted about severe burning and got some great responces.
I haven't mastered the burning but i'm learning to ignore it better. However, I keep developing these huge welts the day or two after the shot. They are enormous and hot to touch, red and hard as a rock. So I try to trooper through it because I was told by the nurse some site reactions will lessen over time. Well, they are only getting worse and the original ones are taking forever to go away. So I called Shared Solutions. I got a nurse who gave me a huge list of things to do differently or try to see if it helps. That was last week. I tried everything on her list and my husband and I double checked everything - and still no improvement. Some of the older spots are starting to get better - but the new ones are bigger than ever! I am running out of shot spots quickly and can't keep up. So I called my MS specialist. Of course, he only works one day a week in this office so I have to wait a few weeks for an appointment. They are supposed to call me to set something up. In the mean time I chatted with the nurse who showed me how to use the shots and she said to stop immediately and not to take anymore.
So now i'm stuck. No copaxone because of site reactions. Betaseron I broke through on. I'm avoiding rebif and avonex because i'm hoping to get pregnant sometime in the relative future. I'm still on the steroids but I get awful body aches so I was hoping to come off them. Ugh! It's so frustrating!
just venting...
Shell
I haven't mastered the burning but i'm learning to ignore it better. However, I keep developing these huge welts the day or two after the shot. They are enormous and hot to touch, red and hard as a rock. So I try to trooper through it because I was told by the nurse some site reactions will lessen over time. Well, they are only getting worse and the original ones are taking forever to go away. So I called Shared Solutions. I got a nurse who gave me a huge list of things to do differently or try to see if it helps. That was last week. I tried everything on her list and my husband and I double checked everything - and still no improvement. Some of the older spots are starting to get better - but the new ones are bigger than ever! I am running out of shot spots quickly and can't keep up. So I called my MS specialist. Of course, he only works one day a week in this office so I have to wait a few weeks for an appointment. They are supposed to call me to set something up. In the mean time I chatted with the nurse who showed me how to use the shots and she said to stop immediately and not to take anymore.
So now i'm stuck. No copaxone because of site reactions. Betaseron I broke through on. I'm avoiding rebif and avonex because i'm hoping to get pregnant sometime in the relative future. I'm still on the steroids but I get awful body aches so I was hoping to come off them. Ugh! It's so frustrating!
just venting...
Shell
