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Vivid dreamsPM

A MyParkinsonsTeam Member asked a question 💭
Rocky Mountain west

Quite often People with PD (edited just for E & A) report thrashing or fighting in their dreams and acting this out while sleeping, so their partner must sleep elsewhere.
But sometimes those vivid dreams are powerful and life-confirming.
Tell me about your dreams -

October 14, 2022 (edited)
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Answer Summary

Members with Parkinson's connected over the topic of vivid dreams, with many sharing that they experience intense, active dreams that include... Read more

Members with Parkinson's connected over the topic of vivid dreams, with many sharing that they experience intense, active dreams that include yelling, thrashing, punching, and sweating through the night, often leading to sleeping in separate rooms from their partners. Several members offered helpful insights, including the possibility that REM Sleep Disorder (RBD) may be a factor, that medications like carbidopa-levodopa may play a role, and that daily napping and Rock Steady Boxing helped reduce dream intensity for some. A recurring theme was finding humor and community in these shared experiences, with members also noting that dreams sometimes offer a joyful escape where they can walk, run, dance, and move freely again.

A MyParkinsonsTeam Member

Yes for awhile I also had these, however they are far less wild today. A suggestion was given to me to nap during the day. The belief here is that stress build up during the day increased the issue. I now nap daily from 1400-1500 daily. This has not stopped them but calmed them down a lot.

May 8, 2023
A MyParkinsonsTeam Member

RSD (REM Sleep Disorder) Talk to your Neurologist there’s medication for it.

October 29, 2022
A MyParkinsonsTeam Member

@A MyParkinsonsTeam Member - I apologize for using the term "Parkies" if you really don't like it. I suppose the politically correct term is PWP (People With Parkinson's, or Person With Parkinson's). I like "Parkies" because to me it minimizes the disease, & anything I can do to minimize PD for myself & for others, I will do. To me PWP seems impersonal, but I will be happy to use it on MPT as long as you & I are both members, which hopefully will be a good, long time!

October 25, 2022
A MyParkinsonsTeam Member

DaleBurton every summer is like that in Ireland lol

June 27, 2023
A MyParkinsonsTeam Member

https://parkinsonsdisease.net/clinical/vivid-dr....

May 24, 2023

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