Received Diagnosis of BFS?

smithylab

Well-known member
I was just thinking today how many of you have an actual diagnosis of BFS from your Neurologist or doctor? If you did receive a BFS diagnosis, how was it determined (EMG, clincial, bloodwork, etc.)I myself have had symptoms for about 7 months now and don't have a BFS diagnosis. Actually, I don't have a diagnosis of anything at the moment, just anxiety. All of the doctors I have seen said my symptoms are caused by anxiety and stress from having a baby. I have diagnosed myself with BFS, even though I've never had an EMG.
 
Four neuro clinicals and one EMG have led my doctors to the conclusion that what I have is "consistent with benign fasciculation syndrome."As for your not having had an EMG, I wouldn't sweat it if I were you. They are vastly overrated, even as a means of sinply attaining "peace of mind".
 
I had an EMG and my neuro said that my fascics were benign, however, he never gave me a formal dx of "BFS." In fact, he labeled me as anxiety disordered and kept prescribing Xanax. After finally overcoming my fear over being dx'ed with MS, I found this forum and actually told my GP that I thought I must have BFS, and he agreed with my self-diagnosis. I had a lot worse symptoms than fasciculations, however. If I'd only just been twitching, I probably would have figured it out a lot sooner. Blessings, Sue
 
After my EMG my neuro said "likely BFS" but that it was too early to tell... So for now I diagnosed myself with BFS and hopefully next follow up will confirm my dx :)
 
my medical diagnosis is benign myoclonia to now which I believe is same as BFS.I definitely have hypermobility (one just have to look onmy shoulders or fingers :))) and possibly some fibromyalgia-like syndrome (what else could give me bloody pains and cramps in all the body muscles (preferred left however) with clear tender points aching as a hell!)
 
Hi Jay, how are you these days? For me, as they couldn't find anything my neuro told me it's 'likely' benign. I had one EMG to check for carpal tunnel syndrome. Lately I wonder if I suffer from fybromialgia.
 
My neuro told me nerve hyperexcitability and told me there was no name for this disease that I can call it spasmophilia or fibromyalgia if I want to.
 
Hi Jay, still around alive and kickin' :D) just like you some days are better than others..... still having arm issues but not as bad as in the first few months. Lately I experience some more twitching in the arms and my eyelids are twitching like crazy the last few days. But we have to stay positive, go out and enjoy life ;) Take care, Fjordian
 

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