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Trigeminal Neuralgia
I have multiple sclerosis and trigeminal neuralgia. My dilantin totally helps the pain, but I have a sensation of internal heat in my face, head and neck. I am wondering if anyone else deals with this.
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Trigeminal Neuralgia is a battle that I too have faced for a long time with my MS. It was my 'onset' symptom as far as I can tell. Do you believe the heat sensation is coming from the medication? I'm not familiar with that drug. I ask because while I have T.N., I also experience burning in my head (left side primarily - also where I have the T.N. attacks, except when I have 'atypical' T.N. attacks that are less severe and affect both sides of the head), and burning in my mouth. I have to take 2 medications, one to control the burning in the skull/head, the other to help control the burning in the mouth. |
Welcome Shaunna, nice to meet you.:)
I don't have TN, thank heavens, but some here do and I am so sorry for your pain..:( I hope you pull up a chair and join us. Feel better soon..:hug: |
Hello Shaunna ..... welcome to NeuroTalk. :hug:
I am very sorry that you are suffering from this symptom. I too have had it, once, and I thank the Lord that it's not recurred. I was treated with a different antiepileptic medication to Dilantin, but I ended up with a course of cortisone to rid myself of that terrible pain. Maybe that's something to think of if the symptoms continues much longer. May I suggest that you have a look at our Trigeminal Neuralgia Forum because the pain is the same, no matter what the cause. This is a really good thread for explanations: http://neurotalk.psychcentral.com/thread27175.html ... and there are more up in the stickies as well. Here's the link to that forum. Do go have a read, even if you don't post. http://neurotalk.psychcentral.com/forum26.html I hope it eases soon for you. :hug: |
hI!
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I'm so sorry that you're suffering Carlisa. Have a look at the reply above my post here, and your post above. Hopefully you will find some information there to suit you too.
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Welcome to NeuroTalk Carlisa, nice to meet you.:) I'm so sorry for both of your DX, especially TN, because that is so painful. I hope that you and your Doc find the right combo of meds to help you.
I'm glad you found us and I hope we can get to know and help each other..:hug: |
I have had trigeminal neuralgia since the early 90's. I suppose there are varying degrees of severity because I was easily controlled with Tegretol. When I was first put on it and with each increase in dose I was pretty drowsy but that would go away in about 2 weeks. I guess it would be considered an abuse of the drug but sometimes when I can't sleep I take an extra dose of it. Since it is more milligrams than I take every night it does help me sleep. I take 200 mg in the morning and 400 mg at night.
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Seems to be the medication that's provided me the most relief. Seeing a pain specialist was one of the best 'decisions' I've made in managing my MS and symptoms (including the T.N.). |
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