Turning my Deep Brain Stimulation On and Off Two Years Later

It has been over two years now since I had my DBS fully set, and I wanted to see what my life would be like without my DBS. I had not turned it off since the last video I did of it two years ago . I was amazed to find out just how severe things were with it off! I am so thankful that DBS lets me live my life with Juvenile Onset Parkinson's. I also discuss my recent program setting change from a pulse width of 60 to 90, which has made a huge difference! progression happens, luckily there are things they can do with the DBS to combat that. The video two years ago found here:    • Turning my DBS off! [Juvenile Onset Parkin...