Trigeminal Neuralgia Awareness Day - October 7, 2013

208 Letters Sent So Far

We need access to treatment and resources for everyone no matter where we live.

We will have ongoing research by Facial Pain Research Foundation and Facial Pain Associations

We need new medications to target the Trigeminal Nerve.

We need donations to go to Facial Pain Research Foundation for a cure.

We need awareness for proper diagnosis.

We need understanding of such illness to obtain benefits for disability.

We need more Neurosurgeons specializing in the treatment of Trigeminal Neuralgia Disorders and Facial Pain Disorders and information about the treatment of these diseases.

This will benefit and save the lives of those that suffer with Trigeminal Neuralgia and Facial Pain Disorders.

Thank you for your support.


Brad Proctor Jr

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If there was ever a cause that needed support it is this one!
My Mom was diagnosed on 1/1/14, underwent Gamma Knife, and is now going for the Key Hole on 10/6. There needs to be A LOT more done, it is a terrible disease.
I Have Neuropathic head pain from a TBI.
Similar to Gabby Gifford's, surgery but in my case, both sides of my skull had to be removed.
A Special day is ok but no more pain is what I seek.
God Bless
My family has lost me to this. A 40year old wife and mother. This disease has not only caused me pain beyond comprehension, It's caused emotional and mental pain... Please HELP US!
I've had this dreaded disease for 9 years on both sides of my face. I fear the day I'm immune to the medicine that keeps me functioning, and I'm one of the young one's that can't afford to have that happen. All of us TN people need more help.