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#11 | |||
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Grand Magnate
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Aleve is Naproxen . . . they are the same drug. The only difference is the dosage.
http://www.medicinenet.com/naproxen/article.htm If someone requires 1000 mg of this drug a day though (Aleve is only 220 mg), they need to be monitored by a doc. This is true especially if they need to take it a fair amount (which I have had to in the past). Cherie
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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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#12 | |||
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Grand Magnate
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Quote:
![]() Cherie
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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 (08-16-2008) |
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#13 | |||
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Magnate
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Maybe that's it Cherie. I don't know, I'm done playing guessing games. I just have to get through the rest of the day, tomorrow, and then see my neuro 10am on Monday. I'll probably feel much better after seeing him
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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: | weegot5kiz (08-16-2008) |
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#14 | |||
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Magnate
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Oh yeah, so tonight the pain was horrible. I grabbed my cold pack from the freezer and put it on my head (kinda just covering the top half of my forehead and the scalp a bit). Upon putting the cold pack on my head, the pain started to go away immediately. The same is true if I put the cold pack on my cheekbones etc.
SO weird! At least I found something that provides a bit of relief. It's like the nerves are freaking spasming in my face. I can kinda feel em in my cheeks right now firing off like little firecrackers. Edit: Not so weird. I began reading about TGN or TN on the net after making this post, and one thing I saw mentioned was that cold relieves the pain with the condition. I wasn't too happy to see stuff like 'oxycodone' mentioned for long term treatment however.
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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 Last edited by dmplaura; 08-17-2008 at 04:51 AM. |
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"Thanks for this!" says: | weegot5kiz (08-17-2008) |
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#15 | |||
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Fabulous Belizean Member
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Laura, I have TN that hits both sides.
"bilateral" TN is not the usual manner, but it does occur. Trigeminal neuralgia (TN) occurred in 35 patients (1.9%) from a large multiple sclerosis (MS) clinic population (N = 1,882). TN began on average 11.8 years after the first MS symptom but in five patients was the first symptom of MS, preceding the next MS symptom by 1 to 11 years. The onset of MS was later in the patients who had TN, and bilateral TN occurred more frequently than expected (in 14% of TN patients). http://www.medscape.com/viewarticle/431442 Seven consecutive patients with multiple sclerosis and trigeminal neuralgia were investigated with MRI to determine the occurrence of a lesion which would account for the patients' pain. Two patients had bilateral symptoms. http://jnnp.bmj.com/cgi/content/abstract/59/3/253
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And the trouble is... if you don't risk anything, you risk even more. - Erica Jong |
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"Thanks for this!" says: | dmplaura (08-17-2008), weegot5kiz (08-17-2008) |
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#16 | |||
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Magnate
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Wow, thanks for the information!!
![]() This is certainly painful. Ouff.
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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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#17 | |||
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Fabulous Belizean Member
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Laura, I got it first time deep in my right ear, like an icepick stabbing.
thought it was Otitis Media (ear infection) but ENT-guy (ear/nose/throat) said nope, no inflamation. so, I thought maybe TMJ, but dentist said no, and no teeth problems either. so, finally went to neuro, and by then, zings and throbs had spread, intermittently to upper cheekbones, behind ear, temples, and sometimes even by my nose. neuro explained it was the Trigeminal Nerve, and showed me a diagram of the nerve and its branches, which matched up with the pain almost perfectly. he told me that getting pain on both sides wasn't common, but he'd seen it before. not usually on both sides at the same time, it seems to take turns, and he said it was due to a lesion in the "pons" area, I think. anyway, after 20 years of MS, I gotta say, it's my LEAST favorite symptom, because I never know when it's gonna REAR its UGLY head, and take my breath away with the sudden sharpness of agony. Butalbital (generic name for Fioricet) helps some, at least it dulls the pain. hugs, and hope you and your doc figure out what's going on with you.
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And the trouble is... if you don't risk anything, you risk even more. - Erica Jong |
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"Thanks for this!" says: | dmplaura (08-17-2008) |
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#18 | ||
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Member
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Oh boy, Laura. I hope you get some relief soon! Ouchy ouchy!!
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"Thanks for this!" says: | dmplaura (08-17-2008) |
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#19 | |||
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Magnate
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Well the good news is, I was able to get out and get some groceries before the pain began to return, but it's much reduced currently from what it was yesterday.
It's definitely an involvement of both sides, the left being more pronounced. I don't think it's gone yet, but the cold packs and then warm bath (yes, surprisingly I can tolerate this!) I think pushed the pain away. At least I got some relief, even for a brief period ![]()
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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: | CayoKay (08-17-2008) |
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#20 | |||
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Fabulous Belizean Member
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that's good to hear !!
__________________
And the trouble is... if you don't risk anything, you risk even more. - Erica Jong |
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"Thanks for this!" says: | dmplaura (08-17-2008) |
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