Dmytro
New Member
Hello everyone.
I have a (hopefully) short question on ME/CFS diagnosis. I’ve been sick for 7 months now and I have no diagnosis yet, probably because my case is somewhat atypical. Although to me ME/CFS still looks like the most probable explanation.
So, the question is: can ME/CFS fatigue be localized in specific parts of the body? To the point that it is hard to move some limbs in some directions meaning that some muscles are constantly fatigued while others are not? In my case it's hard for me to walk (fatigued legs) but when I sit I feel absolutely no fatigue in wiggling my foot from side to side, for example I find myself doing this involuntarily when listening to music. The pretty similar thing is with my arms--I feel fatigue when moving them in some directions while not others, which seems to me that only some arm muscles are affected.
I think I've read that ME/CFS fatigue is usually more immense, generalized, can be felt everywhere, so I'm curious is someone here with ME/CFS (or maybe someone else you know with ME/CFS) has the similar experience?
Thanks in advance!
I have a (hopefully) short question on ME/CFS diagnosis. I’ve been sick for 7 months now and I have no diagnosis yet, probably because my case is somewhat atypical. Although to me ME/CFS still looks like the most probable explanation.
So, the question is: can ME/CFS fatigue be localized in specific parts of the body? To the point that it is hard to move some limbs in some directions meaning that some muscles are constantly fatigued while others are not? In my case it's hard for me to walk (fatigued legs) but when I sit I feel absolutely no fatigue in wiggling my foot from side to side, for example I find myself doing this involuntarily when listening to music. The pretty similar thing is with my arms--I feel fatigue when moving them in some directions while not others, which seems to me that only some arm muscles are affected.
I think I've read that ME/CFS fatigue is usually more immense, generalized, can be felt everywhere, so I'm curious is someone here with ME/CFS (or maybe someone else you know with ME/CFS) has the similar experience?
Thanks in advance!