Multiple Sclerosis (MS) Support Group
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I was listening to a speech on MS. The lady with MS was talking about her MS story and she said with another look at a new mri, no new spots it was good news. It started me thinking,did I get a new mri to see if Copaxone is working.
My first was 2011 and not about one to see if I am on the right track.
Next time I see him is in May and I will ask him. Any comments???
Should I be worried?
Have anyone heard of PBA?
My first was 2011 and not about one to see if I am on the right track.
Next time I see him is in May and I will ask him. Any comments???
Should I be worried?
Have anyone heard of PBA?
Alfred E. Newman had it all figured out.
I was telling my neuro during my last visit about how easy my heart strings pull these days and my that hometown PC doc said I could be depressed. My neuro said maybe it was PBA; he didn't think I was depressed. I don't know much about PBA but choose not to let it bother me and if it bothers someone else it's their problem.
If you aren't experiencing new symptoms I don't see a need to have another MRI. If new symptoms appear or existing ones keep worsening then maybe. I don't see how they can be good for you, the torpedo tube is too small and they play the worst techno music i've ever heard.
I think that you are on the right track. Make a list of questions you have for him and make sure you bring it. Best of luck to you. Request a MRI if you want to make sure that the Copaxone is working.