Quote:
Originally Posted by Dejibo
when I quit copaxone, they really gave me a hard time, and scared the DH to peices. Kept saying that I would end up in a wheel chair, and how dramatic the next flair would be, and did I really want to risk that?? it was so scary! it was THEM causing the stress, and trying to make me feel like I was quitting on myself.
I will tell you in the year since I quit I am healthier, stronger, faster, in a better mood, and can get more of my life completed without dragging thru my day sick and beaten up.
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I just hate to hear about doctors using scare tactics to get people to take medications. As much uncertainty as there is about MS it always amazes me when a doctor can predict something so drastic....such as ending up in a wheelchair. Why can't they tell us when we're going to have an exacerbation......or a UTI.....or ON?
