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Uber, Sorry you are dealing with all these symptoms. It does not sound, to me, like you have MS (my mother and her brother, my uncle, both have MS). I just went to the neurologist and was diagnosed with BFS, and he told me that twitching is not indicative of MS. If you are concerned about MS...

Hi again Renae, Just posting to thank you again for replying to me (Nova). I found your post here and saw that no one had replied, and just wanted to tell you that I'm really sorry you've been dealing with this. It must have been very frightening to go through all that. But, as I said in my...

Hi Renae, Thanks for posting a reply. Sorry you are dealing with this type of thing as well. I did go see the neurologist yesterday. He believes that I have BFS, but is doing an EMG (nerve-conduction) test and checking my Vit B12 levels and doing a brain/spinal MRI as well, to be thorough...

Kim, Thanks for your reply. Even though you haven't heard of facial tightness with BFS, it is nice to recieve a response and know that there is support out there for symptoms like these. I have an appt. to see another neurologist soon, and I hope that will bring some answers my way or at...

Hi Everyone, Don't know if this is the website to be posting this question, but BFS is the only condition that is close to what I've been experencing. I have twitching and a sensation of facial tightness (though I am able to freely move my muscles). Wanted to know if anyone else has...