Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign up Log in
What is This Site Help Center Crisis
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.

Excellent Article. Very Helpful!🍎

A MyParkinsonsTeam Member asked a question 💭
El Cerrito, CA

Does anyone know of any “continuing education “programs for caregivers whose spouses are in stage 4. Can be a podcast, zoom lecture, or even downloadable medical information. I’m the patient and my wife is the caregiver.🍎

November 11, 2023
•
View reactions
Parkinson’s Disease Caregiver Guide: 5 Ways To Support Your Loved One Read Article...
A MyParkinsonsTeam Member

The Davis Phinney Foundation has a book that she can access on the website that is the caregiver version of "Every Victory Counts". There are videos and articles on both the Davis Phinney and Michael J. Fox sites as well that are aimed at caregivers.

November 11, 2023
A MyParkinsonsTeam Member

Thanks Ginny! You are a lifesaver or maybe a marriage saver too? 🤣

November 11, 2023

Related content

View All

Why Do Parkinsons' Patients Have Frequent UTIs? What Can Be Done?

A MyParkinsonsTeam Member asked a question 💭
Fort Worth, TX
May 25, 2024

Has Anyone Else Been Diagnosed With Neuropathy Since They Are On Parkunson's Medication

A MyParkinsonsTeam Member asked a question 💭
Boynton Beach, FL
August 20, 2022

Great Article!

A MyParkinsonsTeam Subscriber asked a question 💭
September 3

Continue with Facebook
Continue with Google
By joining, you accept our Terms of Use, and acknowledge our collection, sharing, and use of your data in accordance with our Health Data and Privacy policies.
Already a Member? Log in