Anyone knows of any FREE resources for someone who has lupus but no insurance?

[otilika]

Hi, I am in Nursing school and recently we learned about lupus. I have a friend who has lupus but only now I know how serious this condition is. She hasn't seen a doctor in almost two years because she has no insurance. She is a permanent resident of the US, works at Olive Garden and is paid by the hour, and therefore doesn't get insurance from her job. She makes around $350-$400/ week, and lives by herself, in a rented room in someone's house, for which she pays $500 + utilities (yes, for $500 in Connecticut you can only get a room). Although she has been stable these two years, I know that it's vital for her to go to doctor's appointments regularly and stay on medications, for which she doesn't have money. I wish I could help her, but have no idea where to start. Does anyone know where someone like her could get treatment an very low or no cost, or any sort of cheap insurance, based on her income? If this was your friend, what would you do?

Thank you very much for any suggestions!