Author: ceddammit

I was diagnosed with Parkinson's Disease (PD) in January of 2015, at the age of 42. Five years later, the progression of PD forced me into an early retirement. It was almost another two years before I finally made this blog happen.

Acting Out Dreams

I regularly complete surveys regarding my Parkinson’s Disease (PD) symptoms and treatments (mostly Fox Insight surveys). One question they always ask is whether I physically act out my dreams (a common PD symptom, it seems). Since I sleep alone, I’ve never known how to answer that one. Until recently, that is.

On one recent night, I fell asleep on my couch. Eventually, I started dreaming. I dreamed I was fighting the Arachnids from the movie Starship Troopers. But not with weapons – I was just punching them. I woke myself up when I punched a canister of snacks I had left on the coffee table. So, now I know the answer to that question. It may also be why Bear stopped sleeping in my room long ago.

Restless [insert body part] Syndrome

I’ve briefly mentioned Restless Leg Syndrome (RLS) in this blog, but haven’t addressed it head-on., so let’s do that, shall we? I have only had three nights of true RLS, which were a result of trying to quit Pramipexole cold turkey. Those three nights kicked off The Worst Two Weeks of My Life. For more on those two weeks, see The Disease. I’ll just say this much for now: thanks to RLS, I now understand the concept of “sleep deprivation torture”. Every single time I was JUST on the verge of falling asleep, my legs would tense up, and I would feel that I HAD to move them around. This happened probably a dozen times each of those three nights.

Since getting myself back on a stable dosage of “prami” I have not experienced true RLS. I say “true” here because I periodically experience what I describe as Restless Arm Syndrome. The sensation is exactly the same as RLS, except it occurs in my arms and/or pectoral muscles. It only happens about once a month, but when it does happen, I just get out of bed. I am not about to put myself through the aforementioned sleep deprivation torture. Sometimes I’ll take an impromptu dose of Carbidopa/Levodopa. That helps sometimes, but not always. Whether I take the extra dose or not, the Restless Leg/Arm Syndrome ceases with the sunrise. Therefore, I think RLS is a vampire.

Introduction (v 2.0)

Are you a new visitor to Voyages with Parkinson’s? Are you wondering what this site is about? Or are you a regular reader who’d like to know more about the origins/originator of the site?

If you answered anything other than “Shit, no!” to any of the above questions, then please see my new ABOUT page by clicking this link.

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