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My latest opus deals with the biggest trigeminal neuralgia [TG] attack I’ve ever had!
‘Recent research suggests that between four and six in every 100 people with MS experience trigeminal neuralgia which is about 400 times more often than the general population. Trigeminal neuralgia is sometimes an early symptom in MS, but it also becomes more likely the longer you have had MS’. MS Trust UK.
The pain is so bad that the Gestapo would just have loved to inflict it!
Anyone been thrown sideways by a sudden [& obvs wrong] abrupt change in medication?
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