International Trigeminal Neuralgia Awareness Day October 7th!

Find a cure please please please.... My beautiful girl is suffering so much

I suffer from tn and in desperate need of a cure

I have had TN for 16 years and so little is known about it by even medical professionals. We need to ensure people understand the horrible painful condition for what it is.

Please help.

I have trigeminal neuralgia. We need more awareness to find a cure.

As a sufferer of TN I believe there needs to be more awareness of this disease. People need to know and be educated about TN. So many, even doctors, have no idea what it is and the magnitude of pain that it causes. Please help spread awareness and help find better treatments for all that suffer from this horrible disease.

I was dx with TN in 2010

This affliction needs more attention paid to its sufferers.

My friend suffers from this and I don't know what to do to help her. Please help.

For my Gina Turner, who suffers from Trigeminal Neuralgia.

My 3 yr old son has TN. Please recognize this disease and help us find a cure. No child should ever have to endure this torture! Would you allow someone to strike your baby with a cattle prod on his face? How about shooting them with a taser? That's how my baby boy feels. And he gets not one but up to 100 strikes a day and night and for up up to 22 hours. Not able to eat, drink, sleep or talk. Please don't turn a blind eye anymore!

I am a Trigeminal Neuralgia sufferer who works hard as an administrator of Facebook group devoted to others who suffer from Trigeminal Neuralgia. Their posts would break your heart! While it is considered a "rare" disease, as more proper diagnoses are made, it's obvious that it isn't that rare. We need the recognition in order to find a cure!

Before making a decision please, please do some research on this so you can understand how horrible it is.Please. Thank you.

My niece suffers from this. It is a painful, horrible thing.

Please let there be a cure my friend wants her life back! Prayers for everyone who is sick with this disease!!!

Please add Trigeminal Neuralgia to the WHO's list of diseases. This is a horrible disease and it's victims need help with better medications and treatments. Doctors need to be better educated on it. There needs to be more research.

Please add tn,we need so much more research.people are killing themselves because they can't live with this disease.

Please recognize this devastating illness. I have trigeminal neuralgia and it's very real and deserving on international attention. I had an MVD to alleviate my pain 7/1/15 and it has worked.

Seeing your sister falling to the ground screaming in horrible pain that she would rather be dead than live with this is something that no one deserves to live with, especially with all the technology we have today. Please put TN on the WHO list and save my sisters ( and countless others) life. Give them some hope to so she can make it thru yet another day of pain and suffering. Please Please

My sister suffers from type one. The pain she is in is horrifying to witness much less live with.