This is a community that supports one another, so I hope you give them a follow and they follow back. We are rare and only those of us with Trigeminal Neuralgia truly understands what each other goes through.
We might be a small community, but our voices are loud. With continued awareness, hopefully that will lead to better treatments and eventually a cure.
If you would like to be added to the Faces of Trigeminal Neuralgia Warrior project, please email me your photo, the year you were diagnosed, and anything else you'd like to share.