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International Trigeminal Neuralgia Awareness Day October 7th!

5,071 Comments

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Donna Pritchett
9 years ago

We need more research for nerve pain, especially from the trigeminal nerve.

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Eden Kecskes
9 years ago

We need to find a cure now!!

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Kimberley Lewis
9 years ago

Have suffered from this for 18 years and need to know that there is being research being done to develop new and better treatments for those who have it and for the young people who don't need to live with it as a live sentence. Please help stop the pain.

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Diane Gorman
9 years ago

This is an awful, hideous and slow death caused by pain. It is living torture. It is abuse and like being imprisoned in an invisible cage because essentially you have lost the ability to be a functioning human being. 24/7 pain wears you down and destroys your body.

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Margie Chodorow
9 years ago

Please do more research. I started with condition over 27 years ago.Would love to see more advancement in treatment in the natural developments.

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Andrea Gentry
9 years ago

I have Bi-lateral TN, symptoms for 13 years before my diagnosis 3 years ago, had MVD (brain surgery ) on left side 11/16/16. Shout it from the rooftops, WE NEED AWARENESS and a CURE!

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Ruth Gale
9 years ago

Please fund research!

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Colleen Newman
9 years ago

I have been suffering from Trigeminal Nuerolgial for over 7 years now. I have had 3 surgeries, and am still in daily pain, while trying to raise a family. Please make TN a priority!

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Jaida Green
9 years ago

I've had TN since 2010.

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Kathy Childers
9 years ago

I have TN. Please add TN to your Health Topics List. Thank you.

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Michele A Freeman
9 years ago

Greensboro, NC, USA

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Chedes O'Neill Sarrionandia
9 years ago

Please also add trigeminal autonomic cephalalgias if it is not already on the list.

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Terri dean
9 years ago

Trying to help

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angel carter
9 years ago

I have TN1&TN2 bilateral, i ave no life, i barely have an existence..... WE NEED RECOGNITION, WE NEED A CURE.

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Nikki Green
9 years ago

❤️

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Deborah Rowell-Sanders
9 years ago

TN warrior here dignosed in 2014

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Margaret Harrill
9 years ago

This is a disabling condition that needs all the force of the attention of the WHO

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Alycia Straughn
9 years ago

Hope you feel better soon, Jeremy Taft!!

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Susan
9 years ago

As rare as this disorder is, this has hit home to me, torturing my son and I recently found out it is also attacking my cousin and a friend of mine. I know the suffering my son experiences and pray for him, my cousin, friend and all who are suffering for answers and most of all, relief

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Kathy Lauer
9 years ago

I am a TN warrior in Ohio. So glad to see so much more awareness since my first attack in 2004.