As we wind down the year with a final couple of episodes, this may be the most important topic. November is caregivers’ awareness month. The Caregiver Action Network (CAN) mission is to promote resourcefulness and respect for tens of millions of family caregivers across the country. This not-for-profit organization is responsible for caregivers’ awareness month. It is vital that we recognize this important person in our lives. They are the unsung heroes in our journey with Parkinson’s or any other chronic disease. They are often overworked, overlooked, and overwhelmed. These important people are part of the care team and should have access to the resources and assistance they deserve.
So, let’s get some insight into the care giving from a couple of real-life caregivers who care for their partners with Parkinson’s. Each has a different situation determined by the progression of the disease, current working status as well as other factors.
This episode is for everyone. You never know when you might become a caregiver for a loved one. 17 Branches and the Parkinson’s Experience recognizes and appreciates all of you who care for your partners and your family.
Happy Thanksgiving. I am grateful for all the people who listen to the Parkinson’s Experience podcast.
https://www.dbsandme.com/en.html
https://www.caregiveraction.org/
https://www.parkinson.org/library/fact-sheets/coping-care-partners
https://www.pingpongparkinson.org/
Thank you to my sponsor, Boston Scientific, the maker of Vercise Genus, a Deep Brain Stimulation or DBS system. To learn more about Parkinson’s treatment options, please visit DBSandMe.com.
Another useful hack is to gently tap your leg if your freeze while walking. (from the last blog)
From this blog:
Dave and Ingrid certainly have it under control. But what happens if you have a spouse (or don’t have a spouse) who can care for you. It might have been interesting to interview care partners who are not spouses (or soon to be spouses). Where does one find a care partner if there is no family member who can care for them? When is it time to start putting your long-term health insurance into play? What if you don’t have long term health insurance? (just some thoughts)