International Trigeminal Neuralgia Awareness Day October 7th!

Had the MVD procedure back in March of 1999, my facial pain returned in Jan 20177! Prayers to all of those people fighting the fight!

This is a terrible disease! I have it and it has taken over my life.

I have experienced this after a MVA and Fx jaw. After my jaw surgery (the 2nd time) the pain let up. At times I still experience numbness along the nerve that goes from the ear to the mid cheek area, neck pain, and atypical horrible head pain on the affected side. Hurts bad.

Diagnosed 1996. MVD with Jannetta 4/99. Pain free until 6/14. Now on tegretol.

This condition is hell day in and day out. And hardly anyone knows or understands. It needs awareness.

Please help stop the suffering for us. It's excruciating pain. We need help. We need funding.

I know the real pain of TN, and would wish it on no one.

Trying to spread awareness to all. So my family, loved ones and friends know what me and others go through daily.

Help us!!!

Trigeminal Neuralgia is the most painful thing I have to endure!!! No one should have to suffer like this! NO ONE!!!!

TN since 1988

Sufferer myself

I suffer with this. Is agonising.

Signing for all those still suffering as I did.

Words are not adequate. This is so important.

This is my world. For all of us who suffer from this, we need help.

Hello. I was recently diagnosed with Trigeminal Neuralgia On July 6, 2017. This condition has put me in an emotional state of sadness. Sometimes I feel like I will lose everything. I am petitioning to fight for a day for those who are suffering from the condition; help those who need a cure and those with medical needs for this condition.

This disease is too wide spread into painful to be dumbed down is no question that should be on the Health list talk topic

Free us from this pain