International Trigeminal Neuralgia Awareness Day October 7th!

Our daughter has had TN for 8 years she is 51 now! It has taken her life away!! Pain is with her daily so she can never make plans to meet friends cause she never knows how she will be functioning. Applied for disability but turned down twice. A very mean disease!! Find a cure!!

Please invest research in this. I feel so alone and so many unanswered questions!

I've suffered with this disease for many years.... Please find a cure!!!!!!!

This campaign needs everyone's support.

We Need Research and a cure. Thank you,

Diagnosed March 4, 2016 I am very fortunate to have a well-informed Primary Care Physician. She knew exactly what to do. Took us a minute, but we found my balance between Carbamazepine and Gabapentin. Still need to FIND A CURE!

Please help us!!

I am 64yrs. old and am entering my 6th year with trigeminal and occipital neuralgia.Keep on fighting

My beautiful daughter-in-law suffers from this illness, please lets find a cure.

[email protected] would love to hear from you if you would like to talk about your pain

Please help make facial pain a thing of the past.

I have been battling TN for nearly 10 years. 3 surgeries & I still have pain. It is just so awful.

I too suffer from this horrible, terrible disease. I am 27 years of age I have had trigeminal neural for 7 years.

I had my lingual nerve crushed and severed after a 3rd molar extraction on April 17, 2015. Initial symptoms included complete numbness of right side of tongue, gums and chin and lip on the right side, front bottom teeth throbbing/sensitive, burning, tingling, stinging, over sensitive, achy. August 2015, I had the neuroma removed and the nerve repaired. April 2016, some feeling has returned to the center of the tongue, however, I still have constant burning, tingling, stinging pain around edges and tip of the tongue (which intensifies after talking/eating). I am pursuing other courses of treatment, a possible 2nd surgery, and a possible lawsuit.

Please find a cure...

Help us, please.

I have suffered from TN for 5 years now, even had a MVD. Give us a chance to live a pain free life, we need more options. WE NEED PEOPLE FIGHTING THE FIGHT WITH US AND MORE DOCTORS KNOWLEDGEABLE OF THIS HORRIBLE DISEASE. GIVE US A CHANCE GIVE US HOPE.

Please add Trigeminal Neuralgia and Atypical Facial Pain to the list of the conditions discussed now!!

Please help us...

people need to know about this terrible disease and the terrible pain people suffer