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Hello List Friends, Just wanted to report that I had the DBS STN done on the second side two weeks ago. Had the first side done about two months ago. I did not want to get my hopes up too much before I went in, you know how it is, better to be surprised by something better than what you expect, than to be disappointed because you set your sites too high. Well anyway the procedure has already done more than I could have hoped for in my more pessimistic days. When I went in to have the stimulator turned on two weeks after the first surgery, I started having dyskenesia as soon as they turned it on . Well the doc said that was a real good sign because that meant the leads were all in a good location. But because of the fact that I still needed the same amount of meds for the one side that was not done yet, they did not leave the stim on then. It was decided to wait after the second side was done to turn them both on. Well that day came a week ago yesterday, they came into my room and turned on both sides of the stim to the minimum. Well I went through about six hours of the most awful dyskenias that I have ever had, because I still had the medicine in my system. But starting the next day, I reduced the meds drastically and each day since then there have been some good signs to report. I wish for all of you that you could have this done. I feel like a person again for the first time in a while. I came home from the hospital today. I was in the rehab unit for a week. I still have a long way to go., but my doc insists that I will be able to walk again someday when I have built the muscles back up in my legs. My medicine is reduced to 1/3 of what I was taking. For any of you that are curious, I am 53 years old, have had Parkinsons for about l4 years, although like so many of you, I had a hard time getting a diagnosis even though my dear brother had it ( also young onset) and I really knew what I had long before I could get the docs to say it. My brother died over a year ago after a long fight with the disease. He died of a massive heart attack. I am not sure how much of that was attributable to the Parkinsons.......but I learned from him to fight and finally I feel like I am back in the ring instead of sitting on the sidelines and watching life pass me by. If anyone would like any other information, please contact me. I will be happy to tell you whatever I can. Diane Leeds [log in to unmask] ---------------------------------------------------------------------- To sign-off Parkinsn send a message to: mailto:[log in to unmask] In the body of the message put: signoff parkinsn