Benign fasciculation syndrome (BFS)
Not sure if this is the right place to ask this, but I'm really not sure how to interpret what's going on. I'm 40, have had random twitches now and then around my body for a few years and ignored them. Mentioned it to my Doctor last year during my annual routine health check and she said it's likely just stress and ignore it. Got sick a month ago, high fever, headache, dizziness, chills, and near constant twitching in different spots all over my body. My knees were going crazy and my biceps were twitching, I felt like my body was malfunctioning. I was also itching all over and my extremities were aching, especially in my feet and hands, but when I pressed or touched my feet or hands, there was no pain spot.
Two weeks after I got referred to a Neurologist who checked my strength, did not do any EMG or MRI, no other tests, just testing if I could physically push back or feel anything below my knees and past my elbows. He laughed and said I have benign muscular fasciculation syndrome and gave me some Xanax. I went for a second opinion and got the same diagnosis, benign muscular fasciculation, and was asked to return after a few months to check on me. The twitching is not as constant as before, but it's still happening, arms, lower and upper legs, knees, neck, shoulder, chest, they last a few seconds and stop. I can't sleep, the itching and the twitching wakes me up at night. The twitching does not go away when I move the muscle, it keeps twitching. Has anyone else ever had anything like this? If so, how or did it resolve?
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There isn't much you can do about it. Try and ignore it and get good sleep. Medicine hasn't studied fasciculations much and there aren't any reliable treatments. It's incredibly frustrating that the syndrome is not researched.
Hi @rtresher1
First of all, kudos to you for being in such good health generally. I don't read a lot of that on these message boards.
This message is not medical advice, just reason to have hope. Just reading your story, my gut reaction is that going off Crestor is related. Like many meds, I read that statins are a med you need to go off of slowly to avoid withdrawal symptoms. I've had withdrawal issues from going off different meds and they can be crazy and last for weeks or months. I also read that one of the issues going off statins can cause is peripheral neuropathy and symptoms of that include twitching and muscle cramps among others. You know the statins caused muscle cramps for you so it makes sense going off of it could impact muscles as well. Since withdrawal is a possibility, it seems there is hope that the fasciculations will resolve on their own. They are very annoying and only noticeable at rest as you have discovered. Good that you sought advice from a neurologist who believes it's BFS and harmless all except for driving you nuts.
I had fasciculations for years starting in my 20s due to my neuropathy then suddenly they stopped from about 40-55 years old. It was a mystery why until I went off atenolol, a beta-blocker for blood pressure. Within days, the fasciculations were back with a vengeance and turned into violent muscle jerks and cramps in my feet and calves within 5 minutes of resting. I was jumping out of my chair and bed all night. I had been on atenolol for 15 years. Aha! I started taking the atenolol again, the cramps stopped and facsiculations improved about 80% over time, but never completely went away again. Darn. Now one of my cancer meds has caused my blood pressure and heart rate to be dangerously low so I really need to be off atenolol as its piling on. I'm trying to wean off slowly this time. I cut my dose in half a week ago and already the fasciculations have really increased in my legs and now in both eyelids which really drives me nuts. No muscle jerks or cramps yet though. I'll do this dose for a month, then if still tolerable, I'll try cutting it in half again and then zero. Not sure I can completely go off, but both my heart rate and blood pressure have already gone up and are closer to low normal now so I'm hopeful I can at least stay on this lower dose for improved health. I really don't like meds. They are a bartering system of trading one issue for another. Sometimes it's a good trade, sometimes not.
Praying that your BFS issues are only temporary. 🙂 Oh caffeine and chocolate (which has some caffeine) will make all my neuro issues worse so maybe test cutting back on any caffeine just to see. Best of luck to you! Zebra
I have had calf fasciculations for so long I can't remember when they became evident. Thankfully, they are pretty localized and don't cause me any problems. Although I have not received a formal diagnosis, I likely have BFS. Reading more about it, I see that it also may be why I tend toward spontaneous muscle cramps, especially in calf and foot, which can be quite painful and troublesome. Those have been a thing from childhood on. I'll throw in yet another possible correlation to the mix of "what abouts."
I had a particularly bad cascade of multiple body-wide, autoimmune-type symptoms several years back following an intestinal viral bout. I eventually found a possible reason after visiting a rheumatologist and getting some genetic testing. I have a particular gene, found by an HLA B27 test, that was triggered, likely by some virus back in my youth, and has been associated with a great many seemingly unconnected maladies. As I researched my own medical history, back as far as my early teens, I kept finding more and more things I have experienced which have since shown a correlation. Some people with it can develop ankylosing spondylitis, reactive arthritis, psoriatic arthritis, uveitis, or inflammatory bowel disease. Most symptoms seem to have an autoimmune correlation. They keep finding more and more possible associations, but since it involves genetic prevalence and often a triggering episode, a lot still needs researching.
I bring this up because it seems that HLA B27 has been at the root of so many of my strange, seemingly unconnected maladies. I just have to wonder whether it could be associated with my fasciculations and cramping. As a matter of interest to others, that particular gene is reasonably rare, about 6% of the worldwide population, but gets more prevalent with northern lineages. Northern Europeans have the highest rates of having this particular gene.
I was diagnosed with BFS, twitching started after my second Pfizer corona shot, so I associate it with that, though no medical specialist will accept that.
I too have gene HLA B27 and also HLA B51 which is probably associated with my uveitis which started in 2015.
Hi Zebra,
Thanks so much for your reply. I have been suspicious about the connection between stopping Crestor and my fasciculations. Do you have any sources or articles you can relate that support your comments about withdrawal issues? I would really be interested in reading them. They really suck. Some days better than others but I can't see any rhyme or reason in them. I had thought about taking Crestor again to see what might happen but don't think I will do that. You're right that all these medications, even the so called benign ones, carry major side effects with them and no two people react the same. Really appreciate your input and help. Cheers. RT
Hi @rtresher1
Just seeing your reply. Naturally, since we read everything online now, I don't have a hard copy saved of what I read. I'll have to look into it and see if I can find what I read about going off statins slowly and withdrawal. If I can find it again, I'll let you know. We probably all do the same thing, query info then start reading and go down the rabbit hole -- click, click, click. 🙂
This is really interesting. I may have some insight. I very recently got very sick… my body almost completely shut down, hand’s completely locked up, my cognitive ability shut down, etc. It was really bad. This was approximately 4 weeks ago.
I’ve been to several specialists to run different tests. One of them being a hormone test. Come to find out my adrenals are shot and my cortisol is flatlined.
I’ve been desperate as I’ve also been having these same twitches for the last week and averaging about one hour of sleep per night.
After learning of my low cortisol levels, my research led me to find out that cortisol is the stress hormone that regulates histamine.
Naturally, if I don’t have any cortisol, I can’t combat the histamine.
But now at least I know what it is. I’m trying some Robitussin PM as an antihistamine as well as hopeful that it’ll knock me out.
But the plan going forward will be to get my adrenals and cortisol levels back up to par to where they can fight the extra histamine.
I hope this helps. Please consider getting your adrenals and cortisol levels checked out.
Sorry I know this is an older post but did you have the twitches all over and sometimes in more than one place at the same time? That’s what I’ve been experiencing
Twitches in different places all over body…. Usually one twitch and done….. not at the same time….. example: a twitch in my elbow then 30 seconds later a twitch in my thigh not always in muscle groups just wherever my nerves are connected
This has happened to me too after my third vaccine in January of 2022. I’ve been to 3 neurologists, switched my GP and run every blood test under the sun. I’ve been told it’s benign fasciculation syndrome and fibromyalgia. I have had some relief from the pins and needles with upping my vitamin D. Still get cramps in my feet behind my knees and pain under my arms. It just sucks.