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July 31
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Answer Summary

Members rallied around the question of losing and misplacing things, with nearly everyone agreeing this is a very common and frustrating part... Read more

Members rallied around the question of losing and misplacing things, with nearly everyone agreeing this is a very common and frustrating part of living with Parkinson's. Several members shared practical strategies that have helped, including giving important items like keys, glasses, and phones a dedicated spot, using sticky notes and door reminders, decluttering the home, and using Bluetooth trackers for frequently lost items. A recurring theme was the importance of being gentle with yourself, leaning on humor and faith to cope, and knowing that this community truly understands the struggle.

A MyParkinsonsTeam Member

@A MyParkinsonsTeam Member, I know that @A MyParkinsonsTeam Member and my Heavenly Father cares about me and my Heavenly Father cares for you, too.
https://open.spotify.com/track/225BdvPD0SoBO7Cv...

Held
Held
August 2
A MyParkinsonsTeam Member

Yea, I have been misplacing all sorts of items for years. Now the tables turned. I have ADHD and for most of my life it has been a been a benefit. I could actually, multitask exceptionally on my past jobs. Now I loose a couple of items at the same time!
To compensate:
* I am Catholic by faith. I have prayed many times over the years for help to find an important items.
* I have reduced many items from my home, I never used.
* If anyone comes in my home and moves anything, I ask that if they pick anything up, for any reason, put it back in the exact place they found it.
* I have reduced misplacing items by teaching myself to put items in the same place, all time. For example, I know where my car keys and my wallet is located all the time. When I use something, I always put it back in the same place I found it.
* By removing many things in my home, I still fall sometimes, but not as much. This is silly but one time I sat down in a side chair and just marveled at all the space I had and still have everything I need. 😊
* I do not cook anymore. I was lucky the two times I did find food that I was cooking, just burnt up, because I forgot about it.
* For my most important items in my house can be located written down on my list, on my refrigerator.
* Loosing items has gotten worse for me, as time goes by during this progressive disease. My Neurological doctor has adjusted my medication to help.
Hope this information helps someone….Gordon

August 1
A MyParkinsonsTeam Member

@A MyParkinsonsTeam Member and @A MyParkinsonsTeam Member, My brain is sharp enough to keep up with 15 to 20 Scrabble Go boards, each playing with one person. Using a stylus pen helps me with a variety of games on my phone, but it seems that every time I adjust my position, my stylus pen disappears. I try to put it somewhere specific, but some way or another, it's gone until I get another stylus pen. ; then @A MyParkinsonsTeam Member will find the first one, or I'll find it looking for the second... or third stylus pen. Oh, well! What can I do?

August 1 (edited)
A MyParkinsonsTeam Member

I would lose my brain if it wasn't inside my head

August 2
A MyParkinsonsTeam Member

Whenever I get ready to go out >I put my phone and my medication together. Several times I can't find them only to find that my husband has put them in his pocket.

August 1

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