Does anyone experience akathisia due Parkinsons?
I was diagnosed last year with akathisia (diagnosed with PD in 2015, but had it since 2012. Other than fatigue, this has been the worst and most prominent of my symptoms. I recently read that B6 will help. I thought it was anxiety; it just causes it. I don't want to have to increase my C/L dosage. I did that already and that took awhile to get over the side effects. Does anyone else have akathisia?
Hi
- How have you been feeling recently? Have you noticed any changes in your akathisia? I can imagine how uncomfortable that is for you and am sending warm thoughts. Posy mentions in a few of their posts that they have experienced akathisia, I linked some below. Although it's not the main focus of the article, I hope it helps knowing others have experienced this too. <3 - Best, Lauren (ParkinsonsDisease.net Team) https://parkinsonsdisease.net/living/side-effect-experience
https://parkinsonsdisease.net/living/work-challenges
