Shoulder Replacement | 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.
Shoulder Replacement
A MyParkinsonsTeam Member asked a question 💭

Today I found out I need a shoulder replacement. Anyone have this done and what were the pros and cons.

posted June 24, 2021
•
View reactions
A MyParkinsonsTeam Member

I pray all goes well. When I had hip surgery, I wasnt given the PD meds until i recovered from the anesthesia and pain meds so if someone goes with you to the hospital, ask them to confirm that you are getting the right med, the right dose, and on time. Many health care providers don't know much about PD or the impact of missing doses. Be your own advocate or bring someone with you to advocate for you.
Please let us know how well your procedure goes. Hope you are back in the boxing ring in no time. LOL
Maria

posted July 10, 2021
A MyParkinsonsTeam Member

Continued-sometimes the doctors are unaware. Thanks Lukas

posted July 8, 2021
A MyParkinsonsTeam Member

Lukas Im so glad that you mentioned speaking to the anesthesiologist. Parkindons meds are difficult To work with because of so many drug interactions and dometime DD

posted July 8, 2021
A MyParkinsonsTeam Member

I'm sorry you have this need but I strongly suggest you make sure the doc treating your PD speaks to the surgeon or anesthesiologist about what anesthesia and pain meds a recommended for people with PD. There are limitations and not all docs are aware of the recommendations.
Maria

posted July 1, 2021
A MyParkinsonsTeam Member

Glad i could help! Believe me i know your pain!! I also had to wait when i finally decided because CoVid was stopping all elective surgery. Hang in there. Because my joint was so bad he had to do a replacement by putting the ball on my shoulder with the socket on my arm. Dont worry if you need this. It works fine!

posted June 27, 2021

Related content

View All
7 Yrs With PD And I'm 73. I Exercise Daily But It's Time To Pursue DBS. If You Have Experience With DBS, What Are You Thoughts?
A MyParkinsonsTeam Member asked a question 💭
Any Wisdom On Dyskinesia And Toe And Foot Spasms?
A MyParkinsonsTeam Member asked a question 💭
Are There Any Averse Reactions To DBS
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