In the last few months I have noticed a buzzing or even fizzing feeling on my feet, particularly my right one. It is very odd and I’m trying to get used to it. Teresa xx
Yep, in my feet, up my legs to half way up the thighs varying in intensity but always there and often in the torso too when at my tiredest. It’s been there constantly since March and is irritating as hell. Muscle twitches every now and then too.
Very weird this neuro stuff
Both of my hands tingle with pins and needles and have been like this constantly forthe last 15years lately I’ve noticed a vibrating feeling and what you describe is what I’m going through.
My back starts to vibrate when I have been for a walk. The vibrations all started mid August, six months after my CIS. I went on an hour long bus ride on a bone shaker bus and sat above the rear wheels of the bus. The bus vibrations seemed to kick of my body vibrations. Now I avoid long bus journeys and don’t sit over the bus wheels. The vibrations started in my lower back, then a few weeks later to my inner thighs and now in my mid back. Its not painfull just a sensation.
I get vibrations too. Inside my chest and stomach and down my left arm and leg. Palm of my left hand and base of my left foot
I get the invisible, internal shaking all over. It,s really weird, and makes me quite clumsy and uncoordinated. I also get the vibrating, buzzing feeling, especially in my feet. I also get the twitching muscles, which is especially severe in my legs at night. In fact, last night I woke my hubby up as one leg was twitching so violently it made the bed shake!
I’m undiagnosed but also get frequent sensations of buzzing and twitching. Does anyone else get the sensation on their scalp as if you are having part of your head shaved with a vibrating clipper? That’s the closest comparison I can make. My lips and left cheek get an odd sensation like a tingle or mild buzz. I got a bit concerned laying in bed the other night when my left arm and leg (and possibly the rest of me in between) had a very mild feeling of tingling, light vibrating. It went quickly but left an impression… These sensations feel like constant little alarm bells going off. It’s hard to have to wait to answer the call. Excuse the 'phone-related pun!
I’m undiagnosed (but have neruo appointment to review MRI today), and I liken it to internal shaking. It’s really strange isn’t it. I sometimes wonder if it’s because I’m hungry, but I eat and it doesn’t help. Some torso twitching too - all very odd isn’t it!
I’m undiagnosed and recently been waking up all twitchy over my legs and my arms. Like Morph I thought it was a bit of my hypoglacaemia. But eating doesn’t work. I’m going back to Dr’s on Tuesday about it. I get this weird buzzing in my chest when my heart races/get palpitations too.
Hi all…I’m new here and after finding this post I feel so relieved. I have had this buzzing/vibration in my legs and feet constantly for the last year and a half and it has now appeared and stayed in my right arm along with numbness in my finger tips. I am undiagnosed still after 7 years, being told that it is a ‘neurological condition’. The neuro put me on Gabapentin for this, muscle spasms and twitches, but after a few weeks of upping the dose, the vibrations come back even harder each time, as if my body gets used to the medication. It is the weirdest sensation and I to ask my husband if he can feel it when he lays his hand on my leg as it is so strong.
Yes. I’ve had buzzing sensation in my legs and back. Pins and needles in my feet and hands. Weakness in my legs, stiffness in my lower back. Numbness in different parts of my lower body. My B12 was low. I am currently in treatment for b12 deficiency. It’s been three months I am getting better. I still have the vibration you describe in my leg and arm, and in my back. But I am far from where I started.
I too have a vibration in my lower back, and it goes up to the back of my head, and my entire head shakes, my body shakes, then my legs and everything shakes. I would love to know what is going on. I am going to the neurologist Friday Feb 7th. I just decided to go there, because I heard online from many people that that is where they are going to deal with this issue, getting EEG or EMG or MRI, ETC. So, I hope to resolve this, my neurologist is very good, I see him for migraines. I am on a lot of medicication, mostly for mental illness, but this is not a side effect for any. So I am baffled.
I am also getting numbeness in my right arm, and it is asleep up to my right hand to my fingers. And, also, I am getting this muscle spasm in my stomach, the upper part right around the sternum area. It happens all the time. I get the feeling, you know, like um… that funny pins and needles feeling like you are about to jump out of an airplane, or lean over a tall cliff or bldg, or about to give a speech, or have that warm fuzzy feeling while watching a romantic comedy that you get when theguy gets the girl, and you feel tingly, you know wt I mean?I get that sensation, I mean, ALL the time, iis quite annoying, it makes me feel cold. It gives me th willies.
Anyways, not to just repeat what every one else said, but yeah, Ireally hope my Dr can come up with something.
Thank you.
Hiya, I’m a 24 year old female and as time goes on I feel I may have MS… I wanted to talk to people who have had similar experiences. Apologies for the long post lol.
My symptoms started in June 2013. They began with an itchy, burning sensation from my elbows down to my hands for a few hours. It wasn’t sore, but annoying. As the days went on, this sensation spread from my neck down my whole arms and hands, across the bottom of my back and down my legs. Then eventually, I had like a shooting feeling down my spine, like an electric shock feeling, a buzzing feeling throughout my whole body and poking feel at the base of my spine. These happened over the course of a few days weeks, at times I was unable to sit. I eventually got in touch with my epilepsy nurse ( I have had epilepsy the past 6/7 years) She mailed back suggesting if it contiues to go to my gp as it could me medication related. I did go to my GP a few days later and she didn’t know what it was, perscribed me co-codamol and an anti-histamine and advised if it continued to go to A&e. I went to A&E, which was a waste of time. I was basically told because I am already under the care of a neuro there is nothing they can do. I battled on with these symptoms until I seen my neuro for epilepsy review in Sep. I explained the symtoms to him and he suggested another brain and full spine MRI, numerous blood tests and I may require a lumbar puncture. He didn’t give any indication as to what it could be and just stated that ‘we have to take this in stages’ . I gathered from his answers, that he wanted to give me a clue as to what it could be but on the other hand he tried to convince himself and me it was musculoskeletal related. I have got all the blood tests (all 11 bottles. I haven’t yet seeked the results but know my b12 is higher than the range) and brain and spine MRI. I went to my GP for the results of the MRI. He gave me a basic overview that I had a herniated disc in t12 area but he was unsure if this would cause the symptoms. The same day I contacted my neuro’s secretary asking if there was anything I could do/ or he advise regarding the herniated disc (if it was causing the symptoms) . He ordered nothing and would ‘discuss everything with me when I see him next’ . He is relucant to perscribe me any nerve pain meds in case to interaction with my epilepsy meds.
I’m due to see my neuro again in March, the time has flown since I seen him last & I actually cannot wait to see him. My symptoms to date have been : buzzing sensation all over body. itchy, burning (nerve) sensation in arms and legs and hands and sometimes right side of stomach. numbness, overheating and prickly feeling in feet, poking feeling in top, middle and bottom of spine. electric shock feeling down spine. Weakness and slight shake in hands (most recently) Random warm hot area in part of my right leg (like hot wax on it). Numbness in alternate fingers or toes. Numbness in left side of lip, and mouth. (like I have been to dentist)Tingling in tongue. Tingling in back passage area and feeling I need to go. Shutter sensation through body (the phrase 'someone has walked over my grave) Dizziness. I also have left mouth spasm but me and my neuro are on the fence as to whether its a seizure as it started a few years back… This has increased since June.That’s all I can recall for now. I have what I now call my 'good days & bad days. I have gone approx 12 days straight without symptoms or episodes and that was over christmas. I have access to all my scans and have had ortho look at them. (I am a nurse and work in an ortho ward) they made no comment or didn’t give their opinion whatsoever regarding the herniated disc and if it could be causing my symptoms. I get the feeling there is something they arn’t telling me. I understand they probably cannot tell me. Of all the doctors and specialists Ive been in contact with since June, noone is telling me their take on it. Two pals told me in the early stages that they think I have MS,one is a nurse and one is a nursery school supervisor. I feel I am mentally prepared for an MS diagnosis but also hope its something simple, such as muscle related or neuropathy or something due to my epilepsy or meds… Has anyone experienced these symptoms prior to diagnosis or has it turned out to be something else? I’m sorry for such a long post. Thank you. If you want to private mail its no probs 
Hi RR25,
sorry that you are getting all these symptoms and have no answers. I am in limbo myself, I have some diagnosis but still have unexplained symtoms which makes life very frustrating.
I can see you spent alot of time putting your post together and deserve more feedback chuck. If you re-post as a new one rather than tag on another heading you may get more feedback. In the meantime I hope you get more answers in March xx
Just to update. I am seeing my neurologist Friday Feb 7th. It has gotten worse. Also, to add, someone said somewhere, not sure if it was here? Or another site? Wristwatches. If you have this vibrating thing, it makes wristwatches stop. I have wristwatches and they have all ceased to work, so I have to take them all to the jeweler. Now I wonder if that is worth it, will they stop again? Is this just for real? I think I tend to believe it tho, because she said it, and it makes sense. Not sure where I read it, cannot remember. I will have to read back to see if it was here or the other site I was on.
I do hope he can come up with a test and not shoo me away. If he does, I will go to another Dr. For sure. I will not give up. This is NOT normal, and is not nothing. It is not in my head. So, I will see. I have fibro. I was also reading about this online, and was told, this is NOT fibro. So, there is that too. Anyways. Good luck to everyone. I will update with my Dr report.
Just to update. I am seeing my neurologist Friday Feb 7th. It has gotten worse. Also, to add, someone said somewhere, not sure if it was here? Or another site? Wristwatches. If you have this vibrating thing, it makes wristwatches stop. I have wristwatches and they have all ceased to work, so I have to take them all to the jeweler. Now I wonder if that is worth it, will they stop again? Is this just for real? I think I tend to believe it tho, because she said it, and it makes sense. Not sure where I read it, cannot remember. I will have to read back to see if it was here or the other site I was on.
I do hope he can come up with a test and not shoo me away. If he does, I will go to another Dr. For sure. I will not give up. This is NOT normal, and is not nothing. It is not in my head. So, I will see. I have fibro. I was also reading about this online, and was told, this is NOT fibro. So, there is that too. Anyways. Good luck to everyone. I will update with my Dr report.
It’s got me bouncing up and down. I cannot wait to see the neurologist.
It’s got me bouncing up and down. I cannot wait to see the neurologist.
This is how I feel most of the time.
Okay, Okay Okay. I went to the neurologist, they say he is the best around. He says it is either my fibro, (knew he would say that), OR it is a pinched nerve, OR it is muscle tissue entering the blood. He ordered an EMG for Thursday Feb 13th.
He did ask me if I had any injuries last year, and I did fall seven times, so he noted that. Not sure if that is what is causing it or has anything to do with it. I am not a mindreader, and he didnt say much about that.
Still bobbing up and down today.