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#1 | ||
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Yes, ATN can be really difficult to deal with - especially the part where the pain just stays and stays. Mine is V1/V2 (forehead and cheek), but otherwise similar. I haven't had anything like you had in the mouth, that kinda sounds like a blister of some sort. I take trileptal, cousin to tegretol, and also take gabapentin and nortriptyline to try to keep it at bay. Also opiates - but mine breaks through nonetheless, so I don't know what help I can offer. I went in to talk with my neurosurgoen again to talk about options (it's a bad sign when you know all of the people in the office!), and he offered to put in a neurostimulator. Officially it's called a Peripheral Nerve Stimulator, and the leads are strung under the skin in the face. It is really a Spinal Cord Stimulator, used "off label", to interrupt the nerve signals in the face. It will be put in on the 1st of September. It will be the first one that my NS has done. ![]() I hope that this helps explain these things, and who knows, maybe it will be one of the things that eventually gets tried on you. For me, ATN has been really hard to get control over, which hopefully is the exception rather than the norm. Do you have a neurosurgeon yet? Hopefully you won't ever need to get that far! Lily ![]() |
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"Thanks for this!" says: | Burntmarshmallow (08-10-2010) |
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#2 | |||
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Junior Member
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Hi Dllfo,
Yes, I also have the ATN diagnosis. Severe pain in the right ear and surrounding area only (so far). I sometimes go for 3 months without an episode, then may have one 3 days in a row lasting 4-8 hours at a time. Carbatrol (extended release tegretol) works better for me than the regular tegretol. I only take the meds when I am experiencing an episode. My heat bag placed on my ear works better than the meds. If you have time to go back and read some of my posts, you may find some more similarities. Good Luck, Rhonda |
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"Thanks for this!" says: | Burntmarshmallow (08-10-2010) |
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