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Ah. this article about TG is a concise primer for a anyone that suffers from it. It is estimated that 4–6% of people with MS experience trigeminal neuralgia. Hullo if u’re one of us,
It first hit me in July 2017 ‘The Mouth that Roared’. Then if really hit me ‘The Mouth That Roared and Roared’ July 1920 = oh, just realized on our third anniversary too. How unpleasant!
As the myelin continued to strip the neuron/s on trigeminal nerve this happened just before last Xmas ‘Well, This Could Be the Last Time, I Don’t Know!’
For now I’ve manage to control it but that’s very much for now.
Please, if u suffer from it, ask questions. Give advice. Have a moan etc.
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