Multiple Sclerosis :: Burning On The Left Side Of Face
Jan 5, 2016
Yesterday after showering I laid down for bed and I got this itchy burning sensation on the left side of my face...I thought to myself it was just dry skin...I woke up the next day with no issue...it was about 34 degrees outside today and wind was gusty...but I maybe spent 45 mins outside on and off...maybe 5-10 mins at a time at best...I noticed throughout my day the burning sensation was getting worse...I came home from work and showered once again and it feels like it made it worse...I am having trouble chewing on that side of my mouth, but only because of moving my mouth to chew...I never had my wisdom teeth pulled and I'm 29 years of age...my teeth and gums themselves do not ache or hurt at all...I just had gotten over a head cold, but i always have them through the winter months...This is the 1st time this had ever happened to me...My skin does dry out in the winter time, but i've never had this feeling before...should i be worried and seek medical help? It almost feels like sunburn and it hurts to the touch...the right side of my face is completely normal...the reason this scares me is if i have a infection in my gums/tooth somewhere i heard this can be deadly if not treated...
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Got ekg test done. It said left leg has irregular complex signals...what does that mean
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Saw my workplace dr today for my periodic health assessment. He asked about my symptoms, I did the required weeping followed by feeling like an idiot for weeping...
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He gave me a prescription for my sinuses, but was rather interested in my reflexes. He didn't say anything but I've had the Babinski thing done enough times to know that one foot was normal, the other was not.
Also, when he did my knee reflexes, my left leg shot out in an exaggerated manner. He repeated it several times, same results. My right leg seems like the usual response, the left was crazy. The left leg has been my 'bad leg' with spasticity etc. He asked me if this was usual, and I said I didn't think so.
He was kind, gave me the usual spiel about neurological issues taking a long time to present, bladdy blah blah blah.
So there you have it, one more 'symptom'.
Dreading the Spring, but trying to stay positive.
I am a 19 year old male. I have a cold sensation in both my feet and hands, this is accompanied by fatigue and heavy feeling hands making typing difficult. I also get relieved by a hot shower (which is weird as the sensation completely goes and this is atypical of MS). This generally causes issues for about 2 weeks at a time and attacks often come 6 weeks apart. I have noticed that sometimes and attack will start after a heavy night's drinking (no I am not an alcoholic and don't drink regularly)
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About a week and a half ago I woke up to my left eye completely swollen shut. Doctor gave me antihistamine and antibiotic to cover allergic reaction and infection. Swelling significantly went down but never 100%. Eyelid still throbbing on occasion and throbbing to side of eye and in corner. Swelling has moved to side of face and under chin. Had cat scan and ultrasound and nothing abnormal but everyone notices the swelling except my doctor down plays it. Something is going and I'm super frustrated with what it could be.
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I was taking a pre workout called mp assault to go lift weights. Then I got strange eye twitching/feeling numb+light sensitivity and dizziness. Now 3/4 days later twitching stopped but more and more of my face is numb and eye doesn't feel right. What is happening?
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I'm 29 years old.
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Since yesterday I've experienced paraesthesia/numbness on the left side of my face.
It starts from just before the eye and to the chin including the left side of my tongue.
A few hours after it started when I saw that this feeling is consistent I went to the ER (it was night so I didn't have many choices).
They did several blood tests, urine test and chest and back X-ray - all came out OK.
They also checked heart-rate and blood pressure and of course they're fine.
I had the same paraesthesia in left side of the face a month ago and it passed within a few hours - the doctor told me then to come back for a checkup if it happens again but didn't refer me to a specialist.
Now they referred me to a neurologist and a nose-ear-throat doctor but I have an appointment for 2-3 months from now.
The last doctor I saw was convened it's an anxiety disorder (which I have for about 15 years) - but it doesn't seem likely to me (although possible).
I also got estimations that it might be a virus or an ear/jaw infection.
Do you have any way to help me understand what i might have and what test should I do (and insist on) and generally, how worried should I be?
I would like to ask about my mom who is 50 years old known case of htn (controlled) and treated case of hepc (compensated cirrhosis).
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She has a history of tooth extraction on the left side 1 yr bacK
she has been having these symptoms of unilateral feeling of heaviness in the ear on the left side and left face below the eyes and forehead and also on the occipito parietal side of the head (left only) .This heaviness when increases turns to a dull ache.she has been having these symptoms with varying intensities almost continuously .It does go away but it comes back.Got her ENT examination done but it was all fine.
I'm 34 weeks and I woke the other morning to the left side of my face paralyzed. I can't move that side of my mouth or close my eye at all and it's starting to droop as well. Doctor said it's called Bell's Palsy and it usually goes away after days, weeks, or even months. There might also be a risk that it could be permanent due to nerve damage.
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Please guide me with available informations for Hematuria having dysmorphic red cells ,pain,left side face numbness.
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I suffer with pain on the left side of my face in the form of tingling feeling in the lip, gum, tongue, nostril and eye. Have been on amitriptlyne for a while and then on gabapentine and pregabalin but the last two gave me awful side effects so have come off them and just taking painkillers at the moment, but they don't do much at all. Has anyone tried a Tens Machine?
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It all started with the feeling of hot water being poured on my right foot. Started out slowly, then became very frequent and has slowly gotten better - now I only feel a sensation of "heat" pressing on my right foot occasionally. The worst of it lasted nearly 8 months. During that time I also had a worsening of many other symptoms such as: fatigue, horrible tremors, dizziness, nausea (from the dizziness), brain fog, chronic headaches/migraines, weakness in my entire right side, thighs that twitch and "pop" when I get warm, severe muscle cramping, vision changes also when I am warm, and urinary frequency problems. I say worsening because I have had some of these symptoms for years and just blew them off. In fact, I had a period of time about 20 years ago when I believe I was having something like the "ms hug" (really sever and unexplained pain in my ribs), as well as a hot feeling on half of my face, and my neurologist at that time said "you probably have some autoimmune disease that will show up later in life". I've had chronic daily headache and migraines for more than 20 years, and an essential tremor for about 10 years that has worsened lately. I also have an unrelated autoimmune disease, which I have been told makes it more likely that I have another (but which one?!). MS was suspected so...
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I've been seeing a neurologist (and a PCP and a rheumatologist) for these symptoms for a while now and feel like I've had every test under the sun. I've had a normal cbc, sed rate, hemoglobin, basic metabolic panel, tsh, b12, all kinds of vitamin and mineral levels, folate, lyme test, MRI of brain and lumbar spine, MRI of brain, and an EMG. I have not had a c-spine MRI and wondering if there is a reason it was not included in these tests. So far the only thing that has come back was a positive ANA (which I believe is from my other autoimmune thing) and a low vitamin D (23), which fell from a level of 58 in under a year. I've been supplementing for more than 4 months. My neuro did not think that ALL of my symptoms could be from the D. Some, perhaps, but not all. Why does he think this, I don't know!
I recently finished a taper of prednisone and feel like the "fog" has lifted, like my brain is working again - hooray. My main symptoms now seem to be fatigue (it's insane), urinary problems, and some newer problems with my left foot (not the foot I was originally having problems with) - where it will cramp up for days and days (two and a half weeks one time), just like a never ending cramp. When it's not cramping I get feelings of heat, or sometimes just a vibrating feeling. The cramping can be very painful, the "hot" feelings are just strange. I've also now started having problems with jumping/twitching muscles in my left hand and arm (different than my normal tremor). I continue to have some right-side weakness.
So I'm wondering, do these symptoms sound as though they could all be because of the vitamin d? I've got a month until I see the doctor again, and he has been trying to push some meds on me, but I wouldn't want to start something if it's all because of the D. Since supplementing, I have had some improvements in my cognitive symptoms, but not much else.
Lastly, my neuro said he may send me to an MS specialist for a second opinion if I am still having problems next month... but if my MRIs are all clean, then there surely must be a more likely explanation, right? I just don't know why he is so sure that the low d couldn't be causing everything. He said that it was very unlikely because my levels had previously been ok and the severity of my symptoms would more match someone who had been very deficient for a much longer time. Does that sound logical? Would an MS specialist be able to tell me anything new?
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Back in March of this year I ended up heading to the emergency room for this strange numbness feeling that began in my hands and feet and then travelled throughout the rest of my body; it lasted about five or six days and then went away completely. I was in the hospital for four days and while I was there I had a CT, lumbar puncture, and an MRI of my brain, all of which were normal. I ended up with a diagnosis of 'post-viral acroparasthesia' and was told that I would be fine.
However, this numbness came back again a couple weeks later. I went back to the emergency room and they said that it wasn't that out of the ordinary for this happen again but gave me a referral to a neurologist who then ordered three more tests: 1) peripheral nerves, 2) evoked potentials, and 3) an MRI of my spine. I've done the peripheral nerve test and that was normal and I have to wait a bit to go to the other tests. I've also had my blood tested for pretty much everything and it's all been normal.
But throughout all the months that I've been waiting to follow-up with the neuro, the numbness as well as some other strange symptoms keep coming out of nowhere (seemingly) and going away. I get really bad tension headaches, lightheadedness, numbness and tingling, fatigue, frequently urinating (sometimes I wake up four times throughout the night), feel a massive brain fog, and more generally I just feel a great deal of malaise. I usually feel like this for four-five days in a row every couple of weeks and then feel completely fine.
These symptoms are pretty ambiguous but MS is something that I'm pretty worried about. My dad has it and is in the latter stages so the doctor's are considering it a possibility. I've seen quite a few doctors now and they haven't been able really figure this out. The most insightful thing that I have been told is that I could have some type of virus, which sometimes may last for a long period of time, and this might explain why I'm getting sick so frequently. I have just been told that I'm going to have to wait to see the neurologist and have anything neurological ruled out.
Whatever is wrong with me is very frustrating. I'm 22 years old working on my university degree and being sick so frequently has taken a huge tole on my academic performance. Also, financially I'm not doing so great and have been cycling through jobs...I mostly end up quitting or getting fired due to the fact that it's been very hard to work like this; it's really causing me a lot of stress.
Prior to all of this I have been quite healthy. I'm very athletic and go out of my way to eat healthy. I don't drink any alcohol, don't do any drugs, and quit smoking cigarettes back in January.
Anything to suggest? Whatever is happening to me is really messing up my life. I can't afford to be so sick all the time and I feel so desperate to know what's wrong.
I have noticed some symptoms that I have developed in recent years that I believe to be symptoms of MS. I am 62, female and concerned that I may have the disease. It's affecting my arm, hand and head and I didn't put it together until I went to a yoga class and it just came to me to check out the symptoms. I have been having tremors, spasms, sometimes painful, in my arm for a few years and it's gotten progressively worse. Last year I noticed my head would shake if my arm was in a certain position. I went to an orthopedist and he said it was due to an old cervical fracture so I let it go. I am going to see my primary doctor and ask for their opinion. But I would like to know if I'm too old to develop MS.
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I am mid process during the diagnosis (I've had the MRI with and without contrast and get results Monday. I'm currently refusing LP and have the evoked potentials scheduled). If I were to be diagnosed (still hoping not) I have read a lot about being gluten free and that helping with symptoms. As a matter of fact, I may try it regardless of diagnosis to see if it helps. But, has anyone with MS tried it? Did it help?
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I was recently referred to a new neurologist. I saw him this past Friday and really liked him. I have had a lot of test run at this point. Including brain MRI which shows what my doctor called one "MS" lesion and one "ischemic" lesion. I am so confused when it comes to lesions. My new neurologist is scheduling a lumbar puncture and will do a MS panel. He also ordered a copper level. Anyone know the reason behind this? I was curious...I don't think I have ever had a copper level done.
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Just about every time I bend my neck forward I have pain that extends upward to the base of my skull and tingling up my head to envelope mostly the upper left side of my head. I am guessing I am having a relapse. I was unable to see my neurologist as its impossible to get in to see him for months. So a local clinic doctor gave me prednisone. So far it's the only thing helping. I have already been diagnosed with Ms but the only thing I have found is people speaking of Lhermitte's that run down the spine. Do I need a new MRI?
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The neuro scrapped the bottom of my foot and could not get it to jump like it used to. he kept trying but nothing happened. I thought this was important but nothing was said and when I asked my physician, he said this was normal. what's it mean if the foot doesn't react?
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Anyone else here experience extremely cold feet? Last night I was up till 3am because they felt so cold. When I feel them with my hands after repeatedly trying to warm them, they don't feel cold to the touch anymore but still feel cold... It got to the point last night where they were painful. They feel cold all day too though I'm able to ignore it somewhat when I'm walking around and doing other things. At night, it's not something I can ignore and it's keeping me awake. What do you do if you experience this? I should mention I've had numbness in my legs below the knee and feet for sometime now.
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I was diagnosed with RRMS in 2000 in the middle of flare which caused numbness in my face and just a weird feeling when I walked. I have been fortunate not to have experienced too many problems aside from a couple of minor flares and the usual fatigue that goes along with MS.
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Last week I was on my computer and all of a sudden I felt like I was not quite sure what was real...thoughts racing from one thing to another. I kept thinking of things and would immediately wonder if it happened. I finally decided to go the the ER. Doc did a neuro exam and said it was OK. I also thought I had a UTI but urine came back clear. He told me to go home and rest. The next morning when I talked to my daughter she said I sounded weird and it was taking me a long me to explain things. The MS nurse also said my speech seemed a little off and slow. Neurologist was out of town but when he came back he told her to call me to set up an EEG because it could have been a seizure. Since then my hand tremor has been more pronounced and weird little symptoms like twitches and sort of an internal tremor in my legs when I walk. I have the EEG next week and then will see my neuro.
I was just wondering else has had something similar. It was distressing to me because I can't really remember things I am usually right on top of; I couldn't remember my meds (I have a list at least). I felt like I lost time and was not sure how much.
Since doctors don't seem to want to help me figure out what's wrong, I'm trying to investigate my various symptoms to find potential diseases to rule out.
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For the past two and a half years, I've had a problem with frequent urination. No incontinence of any kind, but I tend to pee on average 12-20 times a day. Sometimes I'll be up one or two times at night, sometimes more and sometimes not at all. I DO drink quite a bit of fluid. I tend to average 50-100+ ounces of fluid a day. Usually once a day I'll have a cup of tea, but I don't drink a ton of coffee or any soda at all. I am always thirsty, feel dehydrated all the time, mouth is dry, lips are chapped, light headed and dizzy often, even on the days I'm drinking 100+ ounces of water. I work in an office and don't do anything strenuous that results in sweating. When I do pee, sometimes it's only ten or fifteen minutes before I have to go again. Most of the time, I'm producing a full volume of pee, almost never is it just a few drops or a little bit. My urinalysis and cultures come back normal.
Went to the gynecologist today, he said my bladder is working fine and that when I pee, I am emptying my bladder all the way. His suggestion was to drink less. I'm thinking a 31 year old woman who does not have diabetes or a UTI that's lasted for 2.5 years shouldn't not only have this constant need to pee, but also this constant need to drink and feeling of dehydration. I went to a neuroendocrinologist because I truly believe with my other symptoms, I have some kind of pituitary problem going on (Cushings and/or GHD) but he laughed and blew me off because Hey, it's rare, therefore you don't have it.
Should I ask my PCP about looking into MS? In addition to the frequent urination, I have a great deal of cognitive issues (memory loss / retention problems, concentration problems, shortened attention span, sometimes can't speak properly), depression and anxiety, eye issues (wicked light sensitive, blurry vision, hurts to look up or to the sides), stiff and painful joints and muscles, muscle weakness, occasional tingling in hands or feet, INCREDIBLY fatigued, dizziness and lightheadedness, vertigo, occasional balance issues, and trembling / vibrations in body.