Welcome

Please follow TheFacesOfTrigeminalNeuralgia to get to know the Trigeminal Neuralgia Warriors and the year they were diagnosed. 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. 

-Michele