Clonazepam (Klonopin) indeed helped with the pain in my circumstance as well. It is sad that with larger doses, it is very hard to remain cognizant - not to loose or forget things.

1 mg appears to be fine, initial drowsiness and fatigue goes away with time.

Unfortunately, it is not the only medication that I am taking. It appears that my pain is progressing..

What else are you taking Edgaras? I will talk to my dr. about clonazepam. I am taking Ativan at bedtime so I get a good sleep and am able to function in the daytime with some Percocet as necessary. Headaches, face and ear pain are terrible right now as I try to adjust to the new mouthguard.

suboxone, used for neuropathic pain, see - http://www.anesthesia-analgesia.org/cgi/co ntent/full/100/3/781

also, Lyrica and Diclofenac at times.

Recently I am feeling very congested around the right area, my forehead (right side) and even sinuses feel congested even though my nose is not congested. Also I get constant itching and pain in my ear.

It's been tough for past month or so.

i have tried ativan and klonopin but like ativan better b/c i get breathing problems on klonopin and i do aerobic exercise daily and cannot tolerate the klonopin while running or it causes an excessive drop in blood pressure. Ativan is a water soluble benzo and have some different properties which is probably why i can tolerate it better. I have tried a low dose of neurontin before for nerve pain but that drug does nothing for me to really get to the root of the problem of pain which is mucle and nerves. Any gaba agonist should help which is condition but make sure u take a bunch of antioxidents a day to keep them effective as well as eat healthy.

baclofen, zanaflex, and of course painkillers have made a barely noticeable, completely ineffective difference in my TMD. I am completely disabled by it, unable to sleep more than an hour without causing worse-than-migraine pain attacks that include spasms down to my toes, spastic colon, and all the chronic diseases of disturbed sleep. I've just finished 3 whole vials in 3 months of Botox, each vial spread out correctly in 12 injections along the lengths of the masseters and can still chew shoe leather, except for the pain, of course! I find that when the inflammation of my jawbones, face, and facial nerves progresses to the trigeminal and meninges, Relpax helps a little. Also, the attacks are a lttle better after the Botox if I tape my nose shut, sleep on my face, and use the drugstore biteguard that has the springy wings adjustable to mouth size, although it's just noticably less bad, and still leaves me completely disabled. Also, you can't use the Botox for more than a few times or lose the masseters (I had to prove I don't have antibodies to Botox, too). I've gotten every surgery and treathment there is, am broke, and suspect that when I can no longer repair my teeth I'll be cured when they fall out! Any other options appreciated!

heres a shot in the dark...why not try cayenne pepper internally and externally if u have neuralgic pain. I just recently started doing that and the pain has gone down to a more tolerable level. It dramatically increases blood flow and reduces P-factor in nerves to reduce pain. Its worth a shot. It thins the blood only a bit so be careful although i dont think its as dangerous as aspirins blood thinning effects and is way more potent on pain than any herb i ever took...btw i had botox done too and it was useless. I was told to do it again but im debating not to now. For now its ativan for nerves and muscles and cayenne pepper fish oil and msm for this crap. You can try glucosimine chondroitin if ur trying to regenerate the joint. Also ice every day here and there. For sleep you could try melotonin or low dose neurontin. Goodluck on your healing as well.