"I am just going to say: this is such a crappy site. While I signed up for the supposed PsA foundation, there is more information on other diseases available than PsA. In less than 5 years, I have lost so much mobility, have seen a number of specialist, and have been on a ridiculous amount of medication. I am now on infusion, I rejected Remicade, I have what I think is nerve damage in one foot and leg due to breakthrough while on Enbrel. I just would like to talk with others dealing with PsA, but it is hard to find anything that is specific to this disease. "