Hi there. I had an mri scan last week of my head and cervical spine for which I am nervously awaiting the results. This was on the back of some crushing unprecedented fatigue I experienced for about 4 weeks which subsided 3 or 4 weeks ago. I was also suffering from bad brain fog, pain in my hands and feet as well as a stiffness all over my body.
For about two weeks of the 4, I also experienced a dizzy spell every day whilst at work at some point and on standing up it was particularly bad and when I walked the long corridor to the canteen I honestly felt like I was going to bang into the walls. This is difficult to describe but I dont think anyone would have noticed other than me. In other words I dont think it was visual to anybody else.
Now the only legacy of the episode is muscle twitching which seems to happen at rest. I get it in my left foot now but have had it in my calfs, arms and hamstrings to but now its almost exclusively in my foot.
I see a lot of reference to muscle spasms in ms which is different to twitching. To be honest I was terrified I had MND when I felt weak and its still in the back of my mind. Does anyone get muscle twitching in MS and to what extent?