Plus to answer your questions. One side is good enough because even if it was on the other side it would show up because it follows the same tracts in the nerves. So if it was there the emg would show it. Plus the emg just proves at that time it wasn’t present. You really don’t need another emg...
Hi. I am sorry you are going through this. I was in your spot few years ago. Please go on the BFS recovery Facebook to get more help from many people. I can tell you that I am a lot better because y symptoms diminished tremendously at almost three years now. Yes a emg on one side does show...
Hi. Well it will be three years for me this November. I don’t twitch like I used to but I do still have twitches. I think mine started after the illness I had and it damaged the nerve root. I healed from most of the issues I had I do still have days where my facial numbness comes back but...
The part that is upsetting too is the neurologist sometimes think your crazy when you tell them how afraid you are. Then your labeled as having anxiety problems then they send you to get meds. I don't want those but just to know I will be ok.
When I first stretch in the morning I twitch more too. They don't go away rest of day but I have started worrying about my mouth because I can see it on my tongue sometimes when I look. Have you noticed any on your tongue?
I had low vitamin d been on D2 for months with no change so I don't think they have anything to do with twitching. So unless doctor does labs and puts you in it I wouldn't waste my money. I hope you are ok and if you get a miracle cure please post asap!
I even get a twitch on my back and abdomen chest thigh foot hand Literally everywhere. I have had all tests and doctor says BFS. I made the mistake of really researching the worst disease and it really put the fear in me because of how much they stil don't know about detection and there is no...
I wish it was that simple. Even with the two emg I still have the fear. I hope your emg is normal and you stop twitching. I really understand how you feel. You said yours slowed down? How do they feel and do you see them or just feel them?
I have the same things you described started three months ago. It seems the longer it goes on the worse I get. I am in full panic mode. Had all the same tests doctors said BFS. I think I made my neurologist mad because I wouldn't accept that as explanation.
I started twitching after a unexplained health episode where I had right forehead pressure and nausea for several weeks and it went away then facial numbness in the same are then it subsided but came back the numbness then after that I started twitching all over Literally all over then...