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#1 | |||
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Senior Member
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Can you still perform your job as normal with the pain the way it is? Maybe that is the BETTER question you should be asking right now.
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A Hairy Chicken Is Better Than A Hairy Hand! |
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#2 | |||
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Magnate
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Quote:
I'm actually feeling a lot better today. Sure I still have some burning pain and I'm not 100%, but I was relieved to wake up today and have lessened pain. Now we're dealing with 3 days of buckets of rain. Which sucks, but at the same time, it's consistent weather. No pressure changes. That means, no weather influencing my head pains, so hopefully a little break in the chaos.
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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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#3 | |||
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Member
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I hope you can get something to relieve the pain and get relief...something a dental surgeon told me once was to take very warm cloth and put over the jaw joint...then open the mouth enough to get a tooth brush in.
With the end of the brush, lightly massage the very back muscle in the jaw between the gums...it did help some...might give it a try and hope it works for you... ![]() |
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"Thanks for this!" says: | dmplaura (11-08-2008) |
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#4 | |||
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Magnate
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Thank you COK.
I try to avoid the jaw because on top of everything else, I have TMJ. Sigh. That's why I went to the dentist originally, who then told me "You have Trigeminal Neuralgia as well". Could I get any more pain? For seriously. ![]()
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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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#5 | |||
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Member
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Ugg - sounds like a nightmare...so sorry you are experiencing this.
I, too, have TMJ - in fact, my first symptom of the MS was that the right side of my face went completely numb - from mouth to scalp. At first I was certain it was my TMJ acting up - as my jaw was not "hitting" properly. I thought - oh, maybe a pinched nerve. I went to my dental specialist, told him what was going on - and he told me it was NOT the TMJ and to get to a neurologist as soon as possible. (Scary, huh? - but I still had NO idea it was MS - still kept thinking it must be a pinched nerve!) Anyhow - I have heard that cymbalta is VERY good for nerve pain. It is an anti-depressant....it also seems to work well with those who have MS. In fact, I had had drug-resistant depression for years - and then two years ago the doc put me on cymbalta - and voila! Improvement for the first time in nearly 15 years! Again, this was before I knew that I had MS. Might be worth a try? Might even had additional benefits! Good luck - and keep us posted. ~Keri |
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#6 | |||
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Magnate
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Cymbalta's one that's actually in my GP and neuro's offices (right up front) so I believe it's one both fully believe in, and very much could be a possibility. I appreciate the suggestion
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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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