Are you a CPH sufferer like myself? I have posted a forum note on the a hello section. Not much of an IT buff I am afraid. Found out about OUCH recently and think it will be helpful to meet and share experiences with fellow sufferers. Despite CPH a being a rare condition, anyone reading this site will be in the same boat as myself and that I am sure will be reassuring. CPH a sufferer for 3 years. Also have neuralgia on same side of face.
Hope this touches base with fellow sufferer.
Nero
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