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#1 | |||
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Magnate
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Don't know if this is MS, or something else that I had at the time (virus maybe?).
In any event, last year, before my MS diagnosis (fall of 07) I had twitching that began under my right eye. It was non stop from waking to bedtime. I'd had this in the past, but it never lasted for 2 weeks straight! It was very annoying as well as you can imagine. Well, that twitching eventually progressed into my cheek (could see the twitching around my nose on the right), then into my mouth/chin on the right (twitching in the chin). The right side of my mouth looked like it was being pulled upwards. I'd have suspected Bells Palsy if there had been a droop (doctors who saw me at the time thought it may have been like Bells). I had this for 2-3 months (if memory serves me correctly) and then the twitching just stopped. All the while, I had the cruddy burning mouth syndrome (which I still have, hoping that will resolve eventually. it's much lessened now in intensity). I've never since figured out what this facial twitching on 1 side, and the mouth being pulled upwards, could be. Any clues? Could this have been MS? I've looked at stuff in the past, but you know how the Internet is.. ![]()
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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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#2 | ||
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Member
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I've had random twitches since being dx'd, and I never had them before MS. I get them around my right eye, which is also the eye that has the blind spot. Also in my calves which get MS-related spasticity. So IMHO the twitches are somehow related to MS. It makes sense to me, since MS causes interruption in nerve impulses.
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msarkie "Never try to teach a pig to sing. It wastes your time, and annoys the pig." |
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"Thanks for this!" says: | dmplaura (08-26-2008) |
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#3 | |||
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Grand Magnate
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I've had that twitching, which I thought was IN my eye at first, several times, Laura. I saw a specialist (had a couple of eye issues at the time, including waves in my peripheral vision), and he said "although this (twitching) is more common in people with MS, others without MS can get this too". He explained that if it isn't MS-related, then it is probably stress related.
I think what it is (for us) is the Trigeminal nerve. Since I get numbness in my mouth, and at my cheekbone too, I would say I have some TN stuff going on. http://en.wikipedia.org/wiki/Trigeminal_nerve http://www.mult-sclerosis.org/trigeminalneuralgia.html Twitches, pain, itchies, burning, buzzing . . . they are all neuropathic pain reactions, which are sensory symptoms. http://www.mult-sclerosis.org/mssymptoms.html Cherie BTW, if you press the eyelid, the twitching will let up for a while.
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I am not a Neurologist, Physician, Nurse, or Hairdresser ... but I have learned that it is not such a great idea to give oneself a haircut after three margaritas
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"Thanks for this!" says: | dmplaura (08-26-2008), weegot5kiz (08-26-2008) |
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#4 | |||
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Junior Member
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I definitely believe it could be MS. You're RRMS. It came, it stayed a while, it left. Pretty classic IMO. I've had this too before. I've also had eye twitches that have lasted hours or so, hasn't every human? But what you are describing is much different.
Not to dismiss this Sx, but sometimes when I'm wondering if something sensory is MS or not, I think WHO CARES? It's happening anyhow!! ![]() Kimberly
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. This Too Shall Pass . |
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"Thanks for this!" says: | dmplaura (08-26-2008), weegot5kiz (08-26-2008) |
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#5 | |||
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Magnate
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Thanks folks!
Cherie, my dentist suspected Trigeminal Neuralgia all along. When I mentioned that to my neurologist (3 week long headache or migraine, dunno which honestly, with burning pain in my face) he said "Well, that's migraine". ![]() I'll be quite honest, I do believe my first MS "symptom" that presented was Trigeminal Neuralgia. What other headache comes on suddenly on 1 side (4+ years ago, was my left side) and is so painful you're in a ball on your floor clutching your head, thinking you're having a seizure because of the repeated stabbing pain? That's what I thought I had then. Of course, me being a 'stubborn rough chick' I never went to neurologist at that time, and after a couple months and probably this occurring 4-5 times, those severe headaches just suddenly disappeared. I had the spinal headache after my LP and ended up in ER, which if I placed alongside the headaches years earlier with the stabbing pain, the spinal was a 10/10 in pain, whereas the other headaches (suspected TN) were a 9/10. The facial twitching alone would not have been a cause of alarm (was just annoying), but the fact my mouth was pulling up on the right, that's what had me in tears at the time. It was noticeable. I was self conscious going into public with that mouth pull happening. No one noticed unless I mentioned (or maybe they were being nice?) and then they would say "Oh, I see what you mean". That side's never fully gone back to being symmetrical to the left.
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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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"Thanks for this!" says: | Bearygood (08-26-2008), weegot5kiz (08-26-2008) |
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#6 | ||
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Member
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Laura, I don't have TN but I have been visited by "Da Twitch" many times!
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"Thanks for this!" says: | dmplaura (08-26-2008) |
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