Viral Infections :: Sore Throat (feels Like Something Stuck In There)
I've had a sore throat today that mildly hurts, and feels like somethings stuck in my throat. Looking at it it has red and white bumps in the back of my throat, my tonsils are swollen and look raw? There bright blood red patches along with white stringy spots, it doesn't look like strep, but I have occasionally through the years have had random moments when my throat swells up, I also get sore throats a lot the last couple of months. Anyone know what it is?
View 1 RepliesMultiple Sclerosis :: Optic Neuritis - Seeing Stars And Eyelash Stuck In Eye
My right eye has been feeling a little funny lately. Kind of like there is an eyelash stuck in it - but not quite that bad. I've switched to wearing my glasses instead of my contacts, which is helping, but not completely. Today I was seeing stars, it only lasted about 10 seconds and it was completely out of the blue. I am wondering if I should see an optometrist/ophthalmologist. If so, what would they do? It's not like it's a severe case or anything (if it even is optic neuritis). I have a number for a MS nurse, she said feel free to call if I had any questions and I will probably call her on Monday, but I don't want to seem crazy, reporting every single little thing to her.
View 5 RepliesChest Pain :: Sensation Of Food Being Stuck In The Throat/chest
I am experiencing the sensation of food being stuck in the throat/chest, as if you swallowed a large pill and it is resting there. I have had acid reflux issues and take Zantac for it (previously Prilosec) and neither of them helped much. It's difficult to swallow and I also feel like I need to burp to relieve some pressure build-up in my throat/chest.
I woke up out of sleep last night and felt this sensation severely along with stabbing pain in my upper abdomen the radiated up to my chest. There's dull pain in my lower back as well along with nausea, trouble getting a full breath. It's extremely uncomfortable and concerning. It seems to hurt more when lying down, but I feel it when I'm upright too.
I'm waiting on a referral to see a Gastroenterologist to discuss my very extensive list of symptoms.
I understand that it anxiety could add to the pains I'm feeling, and I do have extreme anxiety when it comes to my health, but what I'm worried about is that I woke up out of my sleep with this pain to where it can't be directly caused by anxiety. I've been to the hospital for chest pains a couple of occasions and they ruled out everything but anxiety. So trust me, I know what anxiety can do.
Multiple Sclerosis :: Stiffness And Pain In Neck / Back Of My Head
Just joined and recently diagnosed with RRMS.
I am going out of my mind with worry over some unpleasant symptoms I have been having the last six days.
It started with stiffness in the right side of my neck and at the back of my head, similar to a tension headache but more severe. I have intermittent pain in my right ear, occasional muffled hearing, my neck feels sore to touch, especially at the gland. When I lie down or lean forward/bend over, I have a whooshing sensation in my ears like I can hear the blood pumping.
I have felt dizzy and unsteady at times with waves of nausea.
As I have had no follow up since being diagnosed by the Consultant and have not had an appointment to see an MS nurse yet, I consulted some online MS sites to try and make sense of the symptoms. I thought I may have a muscle spasm and mentioned it to my GP when I saw her on Friday. I was 'told off' for Googling symptoms and told to "stop trying to hang everything on MS".
She ruled out an ear infection or virus and said it was more muscular, however, poo-poo'd a spasm and said it was more likely it was muscular tension following the diagnosis, worrying and getting myself worked up.
It is a different pain to the tension I am used to and tension has never caused me to feel off balance and nauseous. I was given a five day course of diazepam to relax the muscles, however, have only taken one at bedtime on 3 occasions as I need to be able to drive and function at work. They haven't helped particularly.
I was given a 5 day course of Methylprednisolone, 500 mg by the consultant, for neuropathic pain, I finished these last weekend (26th June). A friend who has RRMS suggested it could be side effects of the steroids as her neck and face always swell after she has taken a course and she feels unwell for weeks afterwards.
I am finding it really difficult to function, I just want to lie down all the time and can't get anything done. It's causing me massive anxiety not knowing what is causing this.
Dysphagia :: Tiny Pieces Of Chewed Food Getting Stuck
I'm having a very weird problem for past week. tiny bits of chewed food when i swallow gets stuck back of my throat and takes time and effort to go down. However the problem of swallowing is not there with big chunk of food :S(when i swallow food without chewing much it will be fine.)
Also there is some pain like sore throat..
Throat :: Fingernail Stuck
so i usually bite my fingernails, but this time i was laying in bed and i tried to swallow it but it wouldn't go down. i took some water and i felt a little better. i went to sleep and i woke up and had breakfast. it then came back in the afternoon. i asked my parents about it and they said it would probably go away, but i've been feeling it 4 almost a week. a few days ago it was in my throat and then it went away but then i had a similar feeling in my ear. im worried that maybe its traveling thru my body but im not sur. it might be just growing pains. its now come back.ive had a little shortness of breath but i naturally get that(acid reflux). 1 time it came up a little so i stuck my finger down my throat and i felt it a little, but it felt like it was actually stuck in my throat. like i didn't feel all of it. i tried talking 2 my parents but they told me to stop worrying, but i feel really weird about it, so i thought this is my best option.
View 14 RepliesThroat Feels Like Choking
For the past couple of days, It feels like I'm going to choke on my own tongue. Inside my throat it feels like its being pinched or squeezed and making me feel that I will choke and not be able to catch my breath. I was wondering if anyone can answer me if they know what it might be? Could it be anxiety because i have that sometimes but never like this. And when i was little i had surgery for an cyst when I Tomorrow I'm going to the doctors or the ER.
View 1 RepliesENT :: Lump In Throat Feels Like Ping Pong
I have a lump in my throat that feels like a ping pong ball, it's sore to cough and sends a shooting pain into my chest. The lump is on the left side of my throat and is quite low down, it also seems to be causing pain in my left ear.
View 1 RepliesMultiple Sclerosis :: Vitamin D Or MS Or What?
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...
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?
Multiple Sclerosis :: The Possibility Of MS
Hello everyone,
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.
Multiple Sclerosis :: Symptoms After 50?
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.
View 3 RepliesMultiple Sclerosis :: Gluten Free?
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?
View 4 RepliesMultiple Sclerosis :: Why To Have Copper Level?
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.
View 4 RepliesMultiple Sclerosis :: Reverse Lhermitte's
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?
View 14 RepliesMultiple Sclerosis :: Foot Without Reflex
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?
View 2 RepliesMultiple Sclerosis :: Cold Feet
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.
View 6 RepliesMultiple Sclerosis :: Confusion/seizures
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.
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.
Multiple Sclerosis :: Frequent Urination?
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.
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.
Which Vitamins To Take For Progressive Multiple Sclerosis
First off my name's Katherine and my mother has Primary Progressive Multiple Sclerosis. and I'm here on her behalf. She's in a wheelchair and in a nursing home. She's of sound mind but here lately she seems to be getting a cold and fever every month or so. I know those with MS has very week immune systems and have a hard time fighting off simple colds . My question is what are some good vitamins to help her keep from getting sick as much?
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