International Trigeminal Neuralgia Awareness Day October 7th!

I hope we can find a cure soon!

As a TN warrior, we need a cure!!

This is a debilatating cruel and painful disease. Please help sufferes

Recognize and research ! Don't leave us in the dark.

My daughter, 38, has just been diagnosed with the Atypical Trigeminal Neuralgia. It is by activity of patients and families that rare diseases are given needed attention.

We need cure, my daughter who is currently 16 years old was diagnosed with bi-lateral TN1 at the age of 11 years old. She has currently had 3 failed MVD surgeries and a Gamma Knife procedure. Please WHO bring this to your attention. And helpall these children suffering from this horrible condition.

Signing in honor of my sister Kaleigh.!

For my daughter who is suffering from this horrible pain.

I have Tn since 3.5 years . doctors are not taught enough on it to help. Iam shoved between doctors

Suffer everyday People need to know about TN

13 years and getting worse!

I have Bilater TN, diagnosed in 2014. We need awareness DESPERATELY.

Hoping for a cure!

fellow sufferer

I just found out I have Tn two months ago but I've been in pain for over 2 years

Recently diagnosed and feeling a little uncertain about my future living with TN.

I had over 3 years with Trigemimal Neuralgia. Life hung between blinding lighting bolts of pain and mental fogginess from the search for the right anti-seizure medications. I was fortunate that cranial surgery was able to eliminate the condition.

Stop the pain!!!

This would be great. We need a lot more awareness and a cure

I have been suffering from TN face pain for 20 years