Palsy - Non Cerebral :: Left Eye Would Not Close While Working On Computer
Jan 29, 2007
Yesterday, while working on my computer, I noticed my left eye would not close. Within an hour my lip was drooping and eating was difficult. This morning, my Dr. diagnosed Bell's Palsy and has prescribed a course of steroids. My eye is taped shut to prevent dryness and I feel like I am falling apart,--a a thought that occurs frequently as the my 65th birthday approaches. I have chronic kidney disease and want to know if there is any alternative remedy for this hell known as Bell's Palsy.
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2 days ago I woke up and hopped onto my computer like I do every morning (I'm 16/male and on summer vacation). I noticed that it felt awkward when I tried to blink my left eye. I didn't think anything of it and just continued on with my day.
The next day I woke up to the sound of my phone. I picked it up and it was one of my friends. He told me something that had happened the day before and made me laugh. I noticed that when I laughed only the right side of my face would move. I thought this was very strange and I got a bit scared.
I got off the phone and went to the bathroom and this is where I really freaked out. I couldn't move the left side of my face properly. Everything on the left side seemed a lot weaker than my right.
I tried looking it up for a few hours to see if anyone else has ever had this. I couldn't find anything except for a few forums with people saying it happened to them, but I still couldn't find out if it had a name. I was really scared and was having suicidal thoughts if this turned out to be permanent.
Anyways, I'm very very happy I found this site and that it heals itself. I told my mom and she's going to take me to the doctor so maybe he can give me steroids or something.
Summer vacation ends in about 3 1/2 weeks. I hope I recover by then because I'm not going to school like this, I don't care what my parents say.
I'll keep everyone updated. This is my second day so far with this dumb BP crap.
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My 12 (almost 13) year old daughter is about to get a baclofen pump. She is a foot user as her arms are severely spastic and have a mind of their own. The doctors all say that it will help with her hip pain (she has a dysplastic hip, it is on the leg that she uses) as well as the spasticity and tightness and pain that she has. they also say that it may help with her speech (she speaks very slowly and sometime cannot speak so well as her tightness makes her mouth all wonky).
She has botox about a year ago and it worked wonderfully... for about a week. so the doc does not want to do it anymore. I am totally ok with the pump and she really wants it, but i wanted to speak with others who have CP and have experience with the pump to know what your experience is.
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Day 1
I woke up after having a cold/bad throat for about a week and noticed it was a little difficult to speak. I had a look in the mirror and thought it was because of the cold. By lunch time I could not grip a straw with my lips and one side of my mouth and my cheek would not move properly. I tried to wink or blink and could only do it with one eye and when I tried to screw my face up it only did it on one side. I did think that had a stroke and booked an appointment at the Doctors. She gave me a course of steroids and gave me a leaflet that explains about BP.
Day 2
My eye is a little worse today, I had a little control over my blinking yesterday and today it is almost impossible. It just continually streams that is quite a nuisance. I went and bought some surgical tape to tape it closed with tonight. It is far harder to get food in my mouth today as well as it does not seem to open as well as it did yesterday. On the plus side I do think I still have my taste on the left side. I get pins and needles and twitching around the area of my jaw and my forehead ATM.
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When the heel of both feet cannot reach at the ground in cerebral palsy, what kind of training is considered?
In what kind of training is standing training of cerebral palsy carried out with this institution?
Please let me know the books which can be recommended by home training of cerebral palsy?
Although purchase is considered for the training equipment for functional exercise of cerebral palsy at home, what kind of training equipment is proposed
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I just want to know how the rest of you are dealing with the fatigue of a work day and fighting the fatigue. I'm 38 but most days I feel 108!
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I have a few problems I would like to ask about as I'm unsure if it's just me or not? The first one being my short term memory isn't very good at all, for example if I get asked to do something if I don't write it down I forget very quickly,another problem I have is my sense of direction it's bad. I can go somewhere (through to town) but I can't seem to memorise my way around. I'm now 29 and used to go with my friend every other weekend, no matter how many times we went I couldn't and still can't remember my way around. I hope what I've written makes sense and like I said I'd like to find out if it's a related problem to cerebral palsy or not.
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My daughter was born at 32 1/2 weeks and has very mild cerebral palsy, she is now 17 and experiencing days when she can't get out of bed. She is just exhausted and gets pins and needles. The doctor suggested it could be ME but I wondered if its a result of her Cerebral Palsy. Every time she does something that requires more mental or physical input than normal she is then wiped out for 2 days. Her CP has never really affected her, she wore Piedro boots as a child but recent years has had a "normal" life. Would really appreciate some input, she is due to have an MRI next week.
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I have heard a lot about lengthening the Achilles muscle to ease tightness in order to help kids who have cerebral palsy. My grand daughter finds her physiotherapy sessions so stressful and painful that she's not getting the benefit she needs and I am wondering if anyone has tried this surgery and can tell me has it helped? Any information will be greatly appreciated as it is heartbreaking to see a little one in so much pain and not able to do things a normal child can.
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In 2003 I had really painful headaches so bad I could hardly put my head on a pillow, pretty scary as I do not suffer from headaches. Then as I was eating bowl of cereal I kept missing my mouth and realised I couldn't feel my lips or tongue as though I had been given dentist injection. My sister took me to hospital thinking I was having a stroke, this was the first time I had heard of Bell's palsy and I was given steroids, i was very tired and it was an effort to do anything like eat, speech, it did take three months to go.
february 2014 I got a rash on my stomach which spread to my neck, to my back, to my feet, then to my scalp and then my ears, I was in agony, it was urticaria. Whilst trying to cope with this I then got Bell's palsy again, possibly due to an immune system at a low. However it has taken a lot longer to recover this time. Eighteen months later and I still have a twitchy eye and lopsided smile. I am now considering Botox, has anyone here used Botox to correct any of the nerve damage left after palsy and if so what are your thoughts?
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I am 24 and am suffering with bell's palsy AGAIN. I first had it at the age 18 and also the opposite side which is weird? A couple of weeks ago my 1year old lb accidentally headbutted me and it was 2 days after that the numb tongue and headaches started. Since that my face has drooped as well and can't even close my eye i have 2 young babies and suffer terrible headaches. Im now waiting on an mri to see if there are any fractures on my skull as with a blow to the head can also cause bell's palsy
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I am 36 years old, I am suffering from heartburn regularly with a sharp pain under my left breast close to my sternum. I have been following a low carb diet for 3 months and started cycling regularly. I experience the pain and heartburn while cycling, bending and picking stuff up all the time. I went to the doctor in December last year who had put me on proton pump meds for a month and never had any symptoms. when I finished the course it came back. I do have a bad taste in my mouth all the time and my teeth als feels rough almost.
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The first sign that something was not right was a discomfort in my left eye.While trying to put mascara on my left eyelashes I couldn't bring my eyelid down to meet the brush and on looking in the mirror I noticed that my eye appeared more open than the right eye and on blinking my right eye blinked at a faster rate than the left. Of course panic immediately set in, then I noticed that I couldn't blow my left cheek out as much as my right cheek. I then tried to whistle and noticed that the left side of my mouth didn't look the same as the right. Oh no, first thought was I was having a stroke. My husband immediately ran me to the a@e at my local hospital. After undergoing routine tests and describing my symptoms the doctor diagnosed Bells Palsy and advised a course of steroids and antiviral tablets as well as eye drops to moisten the eye, eye cream to put in at night and tape to stick my eye closed when I went to bed.
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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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I play the French horn and got the Bell's palsy after an exceptionally day playing 3 weeks ago. It seems to be fading already. I was sent to the stroke unit and found to be A1 in all other respects. My treatment was 7 days x 60mg steroids. If I return to playing, will it happen again?
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A person i know has suffered a stroke 8 years ago. He says he woke up at night wanting to go to the bathroom, but found unable to get up. He had his mouth drawn to the right side. His wife has taken him to the hospital. He was diagnosed to have suffered a stroke and had hypertension and hyperlipidemia.
The patient suffers dysarthria without improvement ever-since. Has drooling, fasciculations in the tongue. A small dent in the tongue which (i'm not sure) may be attributed to wasting. Jaw jerk is normal (I think so). No weakness in arms and legs.
What is this condition. IS it Pseudobulbar palsy? (Or a bulbar palsy?)
P.S: There is not pseudobulbar affect in this patient. Can a patient have pseudobulbar palsy without having emotional instability?
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I'm 50 years old with a 9 cm fibroid. I don't have heavy bleeding or bladder problems. The only thing that I feel is some pressure once in awhile and my belly is bigger. Other than that I can live with this. But because is a little frustrating because I do a lot of exercise and my belly does not reduce. I not very comfortable having a surgery , taking my organs out because of something that is not bothering that much. I was considering the UFE procedure but I'm not sure if I'm a candidate since I'm close to menopause.
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I had a outbreak eight years ago. Went all this time until few months ago, had another one. Last week I thought I had yeast infection. Took meds for that but isn't much better. Went to doc today, I have another break out she said. What is going on. Why am I having these two so close together? It doesn't feel the same as last one and that's why I thought it was yeast infection. I have redness and slight burning all over vagina area. She said she saw what looked like a lesion inside the opening of liba. I do have one area that is tender to the touch. I am stressing more than usual last several months. If this is a true outbreak, she did put me on 1000 valtrex, how long should I wait to have sex after I'm feeling normal down there again?
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Anyone else close to due date but haven't had any contractions yet? I'm due in 3 days and NOTHING! any mum's our there who didn't have any contractions/ Braxton hicks and still had baby on time? I don't wanna go over and really need some positive stories.
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Just had a thyroid ultra done..showed a 9.7x7x7 cm nodule adjacent to the left carotid artery (I have lots of cysts which have already been biopsied)..after much discussion we did try to do biopsy, but because I have a short neck, and they were unable to tip my head back enough to do the biopsy without hitting the artery, I was sent home with instructions that I should have another ultra in 6 months..should I be worried, they said its small, but if we can't biopsy it, whats next..I'm off to see my primary doc today..they also asked if I had Hashi's, maybe I should be put on meds to try and shrink the nodule?
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I have been fighting back and forth with myself whether or not I have thread worms. I've gone to great extents to disinfect my house, scrubbing down everything, changing sheets, getting rid of dust, washing loads of clothing.
I know a common symptom is "itching" at night. I've been getting great sleeps, not itchy at all in the night.
What I am worried about is sometimes I feel a wiggling sensation close to the anus. This happens once in awhile. Yesterday it happened twice, about mid day.
I've done the worm tape test, assessed my stool, and haven't seen any sign of them.
I was itchy yesterday afternoon although I currently have my period and often find that I feel a bit itchy whenever I have my period.
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