Does everyone second guess themselves concerning their MS treatment? I was diagnosed April 2010 and started on Copaxone, took it for about 6 months but had to stop due to cost. I was able to get assistance with Rebif so I started that and it made me terribly sick after I had worked up to a full dosage. July of this year I went to Tysabri and I am questioning whether I want to continue.
I know this is a personal question and I am the only one who can answer if it is right for me but does everyone seem to question themselves? I do not feel better after taking Tysabri now for 8months, actually I had a new area in my back start bothering me the month after I started the Ty. I have a huge deductible and then I question whether this is actually working for me.
I had an MRI in my brain only in December and I have no more lesions but they didn't do another one on my spine this time which is where the majority of my lesions were. Guess I am looking for reassurance that I am not in this boat alone here.
I know this is a personal question and I am the only one who can answer if it is right for me but does everyone seem to question themselves? I do not feel better after taking Tysabri now for 8months, actually I had a new area in my back start bothering me the month after I started the Ty. I have a huge deductible and then I question whether this is actually working for me.
I had an MRI in my brain only in December and I have no more lesions but they didn't do another one on my spine this time which is where the majority of my lesions were. Guess I am looking for reassurance that I am not in this boat alone here.
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