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#1 | |||
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Magnate
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As many of you know, I have BMS (burning mouth syndrome), believed to be associated with a brain stem lesion from my MS.
I've been battling this burning sensation since mid 2007. It's truly awful. I have to take Clonazepam (Klonopin) and chew peppermint gum to keep my mouth from being a raging fire of pain (like being scaled with hot coffee, worsening as the day progresses). Today, I noticed an odd taste (at first), then a really odd sensation along the side of my tongue on the right side (where the BMS really did start in my mouth). At first I didn't understand what was going on... it was while making supper that I remarked to hubby, "Oh my gosh, I don't feel burning anymore along my tongue!!!". It's more a numbness with a tiny bit of pin prickly feeling, versus the other side (left) that has the burning mouth thing going full force. Is this possibly my nerve(s) going into a "healing" process? Or re-wiring around the damaged area? Oh I so, so hope the BMS is going away. I haven't done anything special to help the BMS, just taking my medication regularly. NOW if the BMS goes, I can taper off Clonazepam (oh I so want off these prescription drugs). Hope everyone's been well. Been SO busy here. January and vacation can't come soon enough!
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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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Senior Member
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Oh, Laura! I hope it means healing. Nerves do rewire.
ANN |
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#3 | |||
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In Remembrance
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Wouldn't that be great, if He is giving you a break, Laura..
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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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#4 | |||
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Member
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Hi Laura
I have everything crossed for you that a healing process is beginning and you will get some reprieve from this nasty symptom. (((hugs)))
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Lyn . Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993. |
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#5 | |||
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Magnate
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Thank you all for your kind thoughts and comments.
![]() He is giving me a break I believe SallyC. When I was down and out, He was there for me. Each time I prayed with my neighbours for answers, more came in the next day or 2. He is watching his little firecracker of a girl. ![]() Right now I'm dealing with a mouth full of cancer sores. Worst outbreak in a long while. I even had them on my lips (visible a bit). Dreadful pain, but with cankers you can at least dowse them with a warm salt & water mix, swish, wipe the tears off your face, and you get relief for a while. Of course, you ultimately want them gone, and unlike the burning mouth, cankers go away fairly quickly (although there's not been a lengthy period of time during which I've gone completely canker-free since my childhood). Even though I have the cankers, the burning is still absent on the right side from what I can tell! Hope the cankers clear up soon so I can say for sure if my right side has been spared. Left side needs to catch up now. ![]()
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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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Elder
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You have my sympathy--I've been prone to cankers, off and on, most of my life. And worse since MS. But I can't imagine having the constant pain of BMS. I hope it continues to improve.
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* * * **My flesh and my heart may fail, but God is the strength of my heart and my portion forever. (Psalm 73:26) |
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#7 | |||
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Magnate
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Thank you
![]() Right side of mouth feels 'numbish', but importantly, it's not burning still (and I originally noted this December 5 and posted here that day). This is by far the longest I've gone with the burning sensation completely absent from a large area of my mouth. It's difficult to tell how the left side's doing, as I have my cankers there (more of them, argh... non stop!) and a lot of neuralgia pain/migraine/headache and generally messed up sensory on the left. I don't believe the burning is very intense at all - maybe overshadowed by my other aches and pains? I'm really curious if, in the New Year, I can try tapering off Clonazepam slowly. I want to wait still a little while to see if the burning comes back at all, or if it's absent. If it's not back, will have to try taking 2 instead of 3 on alternate days to see if the burning returns. This will be the best Christmas gift ever if the burning is gone for good!
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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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