A forum to discuss and exchange information on the different symptoms of Type I and Type II Trigeminal Neuralgia.
Location: subject-specific group
Members: 47
Latest Activity: Apr 14
Started by Stef. Last reply by Mary Apr 4. 17 Replies 0 Likes
Hello all, I am an Atypical Type II Trigeminal Neuralgia sufferer. Sometimes, I have bad flair-ups without a trigger. However, whenever it is triggered, it is typically chewing, talking, or…Continue
Started by Victoria Swan. Last reply by Victoria Swan Feb 29. 4 Replies 0 Likes
hi as with many of you my triggers are.. when i eat,, i have found stress a big trigger,, laying on my righ sde at night or day if im on the sofa,, closing my teeth together,, on tooth seems to be a…Continue
Started by Phoebe. Last reply by Johanna Smith Jan 14. 4 Replies 0 Likes
Good Morning.Well, not really good for me. I went to bed last night having attacks and upon awakening they started again. I am taking all the meds the doctor prescribed, actually doing a very bad…Continue
Started by aliscott. Last reply by aliscott Jul 26, 2011. 7 Replies 0 Likes
Sorry bout sending this twice - I messed up. I am reading Striking Back and have come across the paragraph about spenopalatine neuralgia, which fits me perfectly except the eye tear and…Continue
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Comment by Pamela K on September 16, 2011 at 10:05pm
Comment by Don Vandenack on July 4, 2011 at 5:31pm
Comment by Stef on May 26, 2011 at 10:52pm Judy,
I have always found Valium a useful medication in my pain control regimen. I am not certain as to why, perhaps it is the muscle relaxant property of the drug. I am not particularly prone to anxiety, more than most people. They often prescribe it for such things. However, it is often prescribed to chronic pain patients.
How is it working for you?
Hugs,
Stef
Comment by Judy D'Arcy-Evans on March 30, 2011 at 9:40pm
Comment by Stef on March 30, 2011 at 9:19pm Hi, Judy.
It is strange. The subject of hormones affecting one's pain was just addressed in another forum. YES! I have ATN, or Type II and my the teeth throbbing, jaw crushing, temple squashing, cheek/palate/tongue burning searing old flair ups I have are MONSTER around that "hormonal" time of the month, for me.
I spent a lot of money on Cortizone injections, when they thought I had TMJ.
A lot of times Atypical TN patients are mistaken for TMJ patients. I see that a lot. That would fall under the "oral specialty".
It would seem that you would be able to call your "shrink" or the pharmacy and see if your prescriptions are safe to take together, or you could wait.
I have found my psychologist has been a most inspirational resource in helping me deal with my chronic pain. I began seeing her after my husband passed away. She encourages me.
I am going back to your page to read your symptoms. I am no doctor. Of course, but Type I, or classic Trigeminal Neuralgia patients usually attacks that are shocking in nature, with triggers like cold, or sometimes even slight touch.
I am Type II, or ATN, Atypical Trigeminal Neuralgia. I am so thankful that I have FINALLY found a doctor who understands exactly what THAT IS! I just wish he were a Neurosurgeon! He's a Pain Management Specialist.
Either way, I hope you find either the medications or procedure which gives you relief as soon as possible.
Wishing you informed and compassionate care!
Your friend,
Stef
Comment by Judy D'Arcy-Evans on March 30, 2011 at 9:03pm My doctor did not say what type I have, as I did not know what I have after being sent on the run around. It seems to get severe around that time of the month and when my usual hormonal migraines happen. Wasted so much time and money going to dentists and oral specialists as they tend to pass me back and forth and then back to the shrink... at least the neurologist who treats my migraines seems to understand but I think he is just going to experiment to see when I take the drugs to see what happens.
I am not going to start them till I see my shrink to make sure it is ok to combine so many sorts.
Comment by Stef on March 6, 2011 at 10:31pm If anyone feels that they fall into the group of Type II, or Atypical Trigeminal Neuralgia, there is a group for this. E-mail me for a formal an invitation, or simply look for the famous painting "the scream" icon and join us.
You never know who you may help with your input.
Comment by Stef on March 6, 2011 at 10:29pm Hello,
Wikipedia provides the most apt description I have read anywhere, thus far, in my online research, on the two types of Trigeminal Neuralgia. Here are the links to the pages which give an in-depth description of Trigeminal and Atypical Trigeminal Neuralgia in that order:
http://en.wikipedia.org/wiki/Trigeminal_neuralgia
http://en.wikipedia.org/wiki/Atypical_trigeminal_neuralgia
Note: My symptoms entirely parallel the description of Type II, or Atypical Trigeminal Neuralgia symtoms.
Reading these pages finally provided clarity to me. I do not use the internet to self-diagnose. My diagnosis of Trigeminal Neuralgia was validated by two physicians so far, the first of which I did not even provide my suspicions to.
However, a third physician I saw after initial diagnosis, called my condition "Atypical Facial Pain" on the order for my MRI. This is a catch-all phrase used to describe many pain conditions in the facial area, I believe, and is not specific to my condition which, in which the pain directly follows the pathway of the the 5th cranial, or Trigeminal Nerve.
I created this page to serve so many facial pain sufferers who join "Living With TN", who do not know what type of Trigeminal Neuralgia they have.
Symptoms of the two types overlap.
Recently, I have been experiencing pain of an intermittent "shock type" quality, which is the hallmark of Type I, Trigeminal Neuralgia. However, I am thankful, that they are not as severe as some suffers experience.
I hope these links are helpful.
If any other members have input, a helpful link to share, or would like to share the stories of their symptoms, please feel free to post a comment or discussion.
As always, wishing informed and compassionate care to all.
Stef
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