Almost there

[bassman]

Indeed Psorinovo is not available in the NHS system. If you want it you will have to pay for it yourself.

I don't know how Joana in Poland has fixed it, but she is ordering it in the Netherlands. Maybe she pays is by herself of maybe the polish health system is a bit more flexible.

Heavy decisions for you as the MTX route is perhaps closed because of your liver.

Still the biologicals like stelara are there.

Definately cannot pay for my medicines Caroline, so NHS is my only option. And yes i agree, MTX is a heavy decision. I know it works, but i also know that i'm one of those who's liver will suffer, but having said that, the blood tests will pick up any problems before i notice its a problem myself

I've already been refused Biologicals, due to cost. I'm not in that percentage of people that have severe P, and Biologicals are reserved those who so much worse off than me, and i'm ok with that. Mine is so minimal, ( couple of small pink patches on upper left leg , its not raised and isn't that raw looking P, rather its just pink) that i shouldn't even be complaining.