I'm fairly sure I'm SPMS. I'm wondering if this means feeling like you're in the middle of a flare the whole time forever, or whether things settle down at some point?
I can cope with gradually deteriorating mobility, but not this constant feeling of being in the midst of a bloody awful flare.
Or it may be Aubagio side effects or the flare I've been in for ten weeks or it may be all three.
Does anyone know whether this is how it is?
I always thought with SPMS, ah well, I might be physically had it, but at least the flares will stop. I never thought it was just going to be one unending flare for the rest of my life. Because if this is how it is going to be, I'm going to need a lot more drugs.
I can cope with gradually deteriorating mobility, but not this constant feeling of being in the midst of a bloody awful flare.
Or it may be Aubagio side effects or the flare I've been in for ten weeks or it may be all three.
Does anyone know whether this is how it is?
I always thought with SPMS, ah well, I might be physically had it, but at least the flares will stop. I never thought it was just going to be one unending flare for the rest of my life. Because if this is how it is going to be, I'm going to need a lot more drugs.
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