just to be sure, you think what happened to me is possible? my MDS is quite skeptical and i cannot find a similar first person account anywhere and i'm reluctant to try pramipexole again just to prove it happened. since that episode my pd symptoms have gotten worse, new chest pains that strangely enough only occur when i'm off. and after 14 years, the off comes on very suddenly, along with rigidity in my feet, left shoulder, right hand, abdomen and newly in my right shoulder. i was approved for DBS but postponed it because i was worried about having insurance in 2017 based on the election results, i couldn't be certain if i would have insurance to pay for anything that might go wrong for 3 years after the operation or if the batteries had to be replaced sooner than expected. i'll be 65 in 3 years. now i'm taking 150mg C/L every 2 hrs alternating/combining with50/200 3-4 times which can give me 3hrs per dose if lucky but this regime is obviously going to wear me out. i guess i'll try the other agonists if i can't get reapproved for DBS.