Has Anyone Experienced This? | MyParkinsonsTeam

Connect with others who understand.

sign up Log in
Resources
About MyParkinsonsTeam
Powered By
Real members of MyParkinsonsTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
Has Anyone Experienced This?
A MyParkinsonsTeam Member asked a question 💭

Hello. I recently had major surgery. Prior to surgery I was in extreme pain and discomfort. I no longer am. My pd meds do not seem to be effective now.

Did you increase/decrease your meds? What were you taking? Thank you

posted January 13, 2019
•
View reactions
A MyParkinsonsTeam Member

My husband reacts very poorly to sedation! It's like PD goes into hyper-drive and the meds don't work at all. On top of that he has vertigo. The vertigo will stick around for weeks! My husband went in for day surgery to get a Spinal Stimulator for pain control (these work wonderfully), but they had to keep him overnight and nearly a second night because he couldn't sit up, couldn't get to the restroom, couldn't get into the wheelchair to go home. Then for almost 3 weeks after, he have severe vertigo, that lessened over the 3 weeks until he was back to normal. Be careful when going under general or full anesthesia if you reacted poorly. Be sure the physicians are always informed you have PD and you react poorly.

posted January 22, 2019
A MyParkinsonsTeam Member

Hi there. My experience with drs is that they tend to overmedicate. I have chosen to tolerate a little more in exchange for less meds and less side effects. Someone living with this disease is more helpful to me than someone who just knows about it.

posted January 15, 2019

Related content

View All
Phila
A MyParkinsonsTeam Member asked a question 💭
Theracycle
A MyParkinsonsTeam Member asked a question 💭
Hello, Has Anyone Had Experience With Trihexyphenidyl As Part Of Their Daily Medications. What Side Effects Has Anyone Experienced?
A MyParkinsonsTeam Member asked a question 💭
Continue with Facebook
Continue with Google
Lock Icon Your privacy is our priority. By continuing, you accept our Terms of use, and our Health Data and Privacy policies.
Already a Member? Log in