Hi Everyone!
can a pseudo exacerbation turn into a flare if you overdo it too much?
I have a big project for work coming up involving 5 days of constant travel and walking.
I am just coming out of a rough time with my walking and I still feel weak, wobbly and more stiff and numb if I do too much.
But this is a project I can not not take part in. (essential to my job).
If I really had to I would take measures to not have to walk so much (arranging unfortunately not very discreet transport for lengthy stretches) but that would involve opening up the topic of my walking/health issues (which I would prefer not to do at this point for many many reasons).
I would only do this is there was a very real danger of a fatigue induced episode turning into a more debilitating episode (one which would not improve with rest).
If not, I would just do my best to rest as much as possible, use my cane and "suck it up" and see how things turn out. (maybe it'll be ok.)
I do not have an diagnosis right now, so its unclear if your input is truly relevant. However, many things I experience fit with what people with an MS diagnosis experience. I would be interested to hear what you think.
Thanks for any input!
Lynne
can a pseudo exacerbation turn into a flare if you overdo it too much?
I have a big project for work coming up involving 5 days of constant travel and walking.
I am just coming out of a rough time with my walking and I still feel weak, wobbly and more stiff and numb if I do too much.
But this is a project I can not not take part in. (essential to my job).
If I really had to I would take measures to not have to walk so much (arranging unfortunately not very discreet transport for lengthy stretches) but that would involve opening up the topic of my walking/health issues (which I would prefer not to do at this point for many many reasons).
I would only do this is there was a very real danger of a fatigue induced episode turning into a more debilitating episode (one which would not improve with rest).
If not, I would just do my best to rest as much as possible, use my cane and "suck it up" and see how things turn out. (maybe it'll be ok.)
I do not have an diagnosis right now, so its unclear if your input is truly relevant. However, many things I experience fit with what people with an MS diagnosis experience. I would be interested to hear what you think.
Thanks for any input!
Lynne
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