Hello,
I was wondering if there are any sufferers and partners of POIS who live in California? It would be nice to meet face to face to support each other.
It also would be a good time to combine our brains on the many forums, doctors, groups, articles and videos (which Im so thankful for because 10 years ago there was nothing!). Maybe a one day power meeting to organized everything we have each learned to help ourselves and others. Interested?