I'm sorry to hear about this -- although I don't know anyone with it, from what I've read, this can be completely devastating.
It doesn't sound like you've gotten hooked up with some of the national groups, though, but are getting your info from "cure promise" sites on the
internet. A lot of them, frankly, are scams that put money in the site owner's pocket while giving you nothing.
I do have friends with severe health problems, and the BEST information comes from national associations for these conditions.
National Psoriasis foundation (if you haven't tried them) has the latest news... I see that they have educational podcasts and have just announced a
new drug regime for certain types of psoriasis.
Check it out: www.psoriasis.org...
And here's a list of many different support groups (in the US) by region:
support.psoriasis.org...
Here's a group you can join where people are discussing treatments and who's done what. This can be pretty useful for you:
dailystrength.org...
Sadly, it's a condition that only 2% of the population has, so it's not one of the "sexy diseases" that gets a lot of money and attention.
Anyway... start with those resources and get involved with an email or discussion board for people with the condition. You'll get far better advice
than from the ol' "google for help."





