mrs d had two severe attacks of stabbing pain in her brain last night, so I’ve been reading up on PHN. Most of the descriptions of PHN seem to be of completely different symptoms, with only passing reference to occurrences of severe sharp pain. Treatment options seem also to be limited, with Zostavax and tricyclic anti-depressants appearing to be the most successful approaches. The first, as poikilotherm indicated recently, won’t even be back on the market until late next year. The other – I wonder how well it really works?
What I also discovered in my reading is that occasional bouts of extreme but transient tenderness of patches of skin that I have suffered for years do fit the descriptions of PHN symptoms. Weird, ‘cos I have never had chickenpox nor have I ever had shingles.
poiky, OCDC, any ideas on how to ease mrs d’s suffering? It’s bruddy scary to be woken by a loud scream in your ear in the middle of the night.