http://www.mayoclinic.com/health/trigeminal-neuralgia/DS00446/DSECTION=1
I hope this helps, and I hope the pain never comes back.
Good day and regards...
I think one of the main issues some people have with Mayo is its conservative approach to treatment. Mayo claims that in early MS with mild symptoms, no treatment is necessary. This flies in the face of what is generally agreed to by other MS facilities, that treating MS early provides patients with the best chance of slowing down the disease process, minimizing the number of releases in RRMS, and mitigating permanent neurological damage.
In 2004 was diagnosised wit TN after many meds that year and losing 40 lbs since I could not eat had a MVD on the left side at the University of Chicago which help alot but pain did not go away altogether and I am still on meds in Oct of this year was diagnosised with Medullary Thyroid cancer at the Mayo clinic and had surgery right away but they did a genetic test since this type of thyroid cancer is heraditery and hard to treat.
4 months ago my stomach lining disappeared and I had all these burns then most recently 2 months ago I was told in an ER I had trigeminal neuralgia which is a very painful nerve disorder in your face. I am only 31 years old. I have been to every hospital and did almost every knee jerk reaction test by most of the neurologists in my area, took a Lyme test and been too mayo clinic. Too me it as if my body is attacking its self.
I was diagnosed a few months ago with trigeminal neuralgia and am wondering if anyone else has experienced symptoms like lazy eye and high heart rate? Am worried because I haven't seen anyone mention these symptoms on any other site.
I may have trigeminal neuralgia in the mandibular branch. Severe pain in the lower gum area but it is on both sides which has my PC doctor, my neurolgist, my pain management dr, my neurosurgeon and my accupuncturist all baffled. Meanwhile, I am on Lyrica, which is becoming ineffective, Vicodin, which does not help much, and Ambien to knock me out at night to get some sleep. Is anyone out there who has experienced such a problem that can head me in the right direction? I am losing hope.
t say for certainty what was the issue is the neurologist says trigeminal neuralgia and the ENT says TMJ. The pain is horrible and is daily. Where my mouth hurts there isn't even a tooth there! So far I have been on tegretol, Neurontin, 800mg ib profufen, Tylenol, vicodin, Tylenol 3, and Norco's and acyclovir (in case it was shingles) not all at the same time. NOTHING works. Well, the ib proufen works but it only lasts maybe 2 hours and I can only take it every 12 hours.
Already she had two pain blocks, neither worked at all and now they want to do a Radio Frequency abrasion - I am concerned about her diagnosis, atypical trigeminal neuralgia -- being treated like the regular Trigeminal Neuralgia, the pain symptoms do not match -- did yours start this was and progress into the trigeminal neuralgia
They have all her dental recorrds, even an MRI plus another ct from emergency room earlier this year, and all the records from the pain clinics -- yet pain symtoms
Traumatic trigeminal neuropathy is generally not associated with trigeminal neuralgia. However, both entities may be responsive to pharmacologic intervention. Seeing a neurologist or orofacial pain specialist misadvised.
Your symptoms do not exactly match the clinical picture of trigeminal neuralgia but you should continue with the treatment and do notgo in for complicated details.The treatment consists of medicines, surgery, and complementary approaches.
For more information refer http://www.ninds.nih.gov/disorders/trigeminal_neuralgia/detail_trigeminal_neuralgia.
Do you think this can still be Trigeminal Neuralgia? Is a neurologist the best type of Doctor to seek treatment from?
Thank you again.
i have a reaserch on mangment of trigeminal neuralgia , but i cann't know until now which the best medical or surgical treatment and i couldn't found which have high rate of recurrance.
Does Trigeminal Neuralgia worsen with age. I've tried Tegretol but the pain has some back agaiin after about a year and is very, very intense. It is like a needle made of glass penetrating the right side of my nose and going into my head. What is the best treatment for this and can it be cured completely.
This discussion is related to <a href='/posts/show/894401'>Trigeminal neuralgia more help</a>.
Hello,
In your case, I think that it can be trigeminal neuralgia. Trigeminal neuralgia is very painful swelling (inflammation) of the nerve (trigeminal nerve) that delivers feeling to the face and "surface" of the eye. Trigeminal neuralgia causes severe, short-lasting (only a few seconds) facial pain on the side of the affected nerve even by slight touch. Mostly affects elderly females. May be caused in multiple sclerosis also.
,
She flew on a plane a few days later and thought her tooth would explode
Pain continued in the tooth with the root canal, was sensitive to heat and cold, and I put ambsol on that tooth only with a q-tip, she felt the liquid on the tooth with the root canal and it was painful, a few weeks later and another root canal, then a crown and two bite gurards in 2 months and still the pain continued -- pain is located on left side of face lower jaw (where the root canals were) later after trips t
Does anyone know an Acupuncturist who specializes on the relief of pain from Trigeminal Neuralgia in the UK/ France/Germany?Brussels?
Any feedback on this appreciated.
Hello,
From your symptoms the possibilities of trigeminal neuralgia and temporal arteritis need to be ruled out. Trigeminal neuralgia is painful swelling (inflammation) of the nerve (trigeminal nerve) that delivers feeling to the face and "surface" of the eye. Trigeminal neuralgia causes severe, short-lasting (only a few seconds) facial pain on the side of the affected nerve even by slight touch. Mostly affects elderly females. May be caused in multiple sclerosis also.
Trigeminal neuralgia can come and go but your statement suggests that you probably had some type of nasal surgery or what is called percutaneous stereotactic radiofrequency rhizotomy, an effective treatment for trigeminal neuralgia and one with lasting benefit. Thus the pain that you are now experiencing is unlikely to be related to the trigeminal neuralgia, as you yourself suggest.
org/posts/Multiple-Sclerosis/Attack-of-trigeminal-neuralgia--OMG/show/2646953#post_12856616) I moaned about it, but I have to say it was excruciating. Fine now, at least from that standpoint.
The standard treatment is Tegretol (carbamazepine). It turns out I can't tolerate that, as a reasonably effective dose wiped out my balance and had me staggering all over the place. It also almost destroyed my platelet count, which was down to 23.
i have been treated for tmj for 5 years with no relief and then i had an arthrocentesis done and still no relief. now my doc tells me i have trigeminal neuralgia and is going to give me an injection into that nerve. what i want to know is there side effects of this injection? and can trigeminal neuralgia cause pain in the back of the head where the skull meets the spine. i have had continuous pain there worse then ever. i am now on neurontin and baclofen and it helps extremely.
Symptomatic trigeminal neuralgia is usually caused by multiple sclerosis or by tumours arising near the trigeminal nerve root.
Differential diagnosis of trigeminal neuralgia:
Cluster headache - Longer-lasting pain; orbital or supraorbital; may cause patient to wake from sleep; autonomic symptoms
Dental pain (e.g.
Recommended
