I was diagnosed with systemic lupus in 1988 and have developed many other diseases and complications subsequently. Several years ago I was diagnosed with PAH. To my knowledge there is no support or advocacy group in my city. I need to talk to others who have PAH; I need to understand how to live with this disease. I have the appropriate doctors—a rheumatologist and a lung specialist—but there is no PAH specialist here. I am currently on Tracleer with no improvement after six months. Can you connect me with others who have PAH? Thanks.