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#1 | |||
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Junior Member (previously Cinderbrat)
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having twitching and have had it befor. when I was 1st dx but the thing is, is their anything I can do to help it not be as bad or go away cause its getting to the point were its annoying and just want it to stop.
if anyone has advice that would be ![]() DX - 4YEARS AVONEX - 1 WEEK |
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#2 | |||
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Magnate
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I was "twitcher" for a few years. It IS annoying!
There were times it would be twitching and not visible but you could feel it under the skin like an electrical current. Mine was always on the right side of my face, but they could pop up anywhere, one muscle fiber just twitching away, almost looked like something alien was trying to get out when it was my leg or abdominal area. I used to put fingertip pressure on the twitch, usually on my eyelid, my undereye area, my cheek or my upper or lower lip. Sometimes it worked, sometimes it didn't. Applying ice to the area for a few minutes worked for me too, when it was particularly bad. Occasionally the facial twitching would spasm and make my face twist up on that side, which was kind of funny when you looked at it clinically (I called it the 'Elvis look'), but annoying as all get out. I would use an ice pack for a few minutes and it would calm down. It's said to fool the nerve or something. Doc said heat and stress make it worse, and called it 'fasciculations'...realllllly? ![]() I haven't twitched in a few years and I don't miss it at ALL! Hope this helps, I truly feel for you on this one!
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I know the sound the river makes, by dawn, by night, by day. But can it stay me through tomorrows that find me far away? . I have this mental picture in my mind of you all, shaking bones and bells and charms, muttering prayers and voodoo curses, dancing around in a circle of salt, with leetle glasses and tiny bottles of cheer in the middle...myyyyyy friends! diagnosed 09/03/2004 scheduled to start Tysabri 03/05 Tysabri withdrawn from market 02/28/05 Copaxone 05/05-12/06 Tysabri returned to market 06/05/06 Found a new neuro 04/07 Tysabri 05/25/07-present Medical Marijuana legally 12/03/09 . Negative for JC virus antibodies! . I'm doing alright and making good grades, The future's so bright, I gotta wear shades! . |
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#3 | |||
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Wisest Elder Ever
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I used to get this. I asked my Neuro about it and he said the same thing, River. Stress. I said I wasn't really stressed about anything. Well, except my eye twitching!
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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#4 | |||
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In Remembrance
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Hi Brat..
![]() ![]() ![]() ![]() ![]() What chu been up to? ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#5 | |||
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Magnate
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Mine twitches off and on.. if I'm stressed (as others mentioned), in poor light, looking at a computer/television/anything digital or electronic display for too long.
Make sure you get as much sleep as possible. I find that getting around 7-8 hours a night keeps mine at bay, but if I go 5-6 hours the twitching will inevitably come back.
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2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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#6 | |||
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Member
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Does the Neuro say this is MS thing? My right eye twitches a lot, was never sure why. My right eye is the one that doesn't seem to open as wide that my co-worker noticed one day. Caused me to go to Dr. and have my first brain MRI, and found lesions. Interesting.....
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"Thanks for this!" says: | SallyC (04-13-2011) |
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