I'm still having the numbness and pain in my hands and middle of my back. Pain down my left leg, all the rest... the usual. I am taking a break from the gabapentin. I just am sick of taking 16 pills a day and not seeing a difference at all. It's only been a two day break so far.
I'm not feeling very happy still. But Winter doesn't help.
To Mike who commented about the Shingles... my Neurologist said that they don't come back and so far she's been right. I'm sorry you're having so many issues. Hopefully you're on one of the injectibles and it will help.
I was told by a friend today that he was talking to his other friend with MS who is on Tysiabri and that she hasn't had a relapse since. I think that's great news. Who knows, maybe I'll switch. Not sure I have the constitution to do that though right now.
This is going to be a short post today.
I hope you're all well or doing better than yesterday.
Take Care,
Pamela
2 comments:
I have two friends on tysabri right now. They have a very agressive MS and they are great since they start with tysabri... it seems it's magical... I've been thinking about it, a lot...
Yeah, I have too - it's scary though... with small kids too. Good luck with everything and take care!
Pamela
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