Errr... neither. The pain is right smack in my hip joints. That would make it cartilage, I think. And it feels like what I IMAGINE rheumatoid arthritis would feel like if I had an active case of it in my hips (which I indeed MAY have). I believe I'm looking to see if it's possible that Mirapex can CAUSE RA to start it one's predisposed to having it, or is in remission - like me - at the time they began taking the Mirapex. Barb Mallut [log in to unmask] ---------- From: Parkinson's Information Exchange on behalf of Linda Carlton Sent: Monday, October 27, 1997 9:36 PM To: Multiple recipients of list PARKINSN Subject: Re: Possible Mirapex Problem? Kathie, Barb, and Marty, My father has reported the same problems, except I cannot get him to describe the pain to me. So I will ask you the same question. Does the pain feel like it is in the bones or muscle? Thanks Linda Forrest's mom PS My father began the mirapex a few months ago. Kathie Tollifson wrote: > > Barb asks: > > >Amongst our Mirapex users, has anyone found that shortly after starting the > >drug they developed continuous pain in their hip joints (or any other joints?) > > > > > > Barb, > > I didn't have hip problems, but I did experience fairly serious pain in my > arms (wrists, forearms, hands). Also a lot of pain in my neck (okay, I know > this is a set-up, but I'm serious). I stopped Mirapex about 3 weeks ago > after reaching a 2.25 mgs/day dose, and I'm very glad I did. It just didn't > work out for me. > > I believe the problem for me was that I couldn't take enough sinemet to > correct rigidity in my hands,forearms, and neck without launching into > totally off-the-planet dyskinesia. Also it affected my mood in ways I didn't > like, and was a SERIOUS sleep-destroyer for me. > > So I am returned to a normally-abnormal condition. I have three friends here > in Tucson using it, one attributes a car-wreck to same untreated rigidity > condition. The other two say they are doing great. > > Kathie Tollifson > [log in to unmask]