Sharing between friends- things you might ask or want answers to episode artwork

EPISODE · Dec 16, 2020 · 39 MIN

Sharing between friends- things you might ask or want answers to

from Lewy Body Roller Coaster

On this episode and the next episode 17, its just Linda and Curry sharing some questions from support groups and responses from the many who continue to share ideas that will help us all through this journey with Lewy Body Dementia.The first two questions are geared more towards caregivers.We discuss how to respond  to people who visit and then say that your loved one looks great or doesn't look like he has dementia.Do you ever get used to the diagnosis or used to what Lewy is doing to your loved one?Finally, we discuss the questions of whether you should wake your loved one for meals and if they are really having hallucinations or seeing ghosts.We share comments from many with helpful suggestions and comments.Shall you wish to bless us with your support you can go to: https://patreon.com/lewybodyrollercoasterpodcastor the GoFundMe page athttps://gofund.me/c416ecb6Patron Shout OutSilver Patrons                                         Bonnie Ziegler-Weber                                  Mark Youlden                                                      Lisa DeRosa                                                                         Gold PatronsNancy GuerroPhyllis BanksCindy      Marcia TreffmanJay MacLeanSheila FureyChris OaksLenny AsuncionPlatinum PatronDarlene Passmore-Armstrong Thomas ConnellyGo Fund Me Shout Outs toLisa DeRoaLaketta MitchellLori CragHeather and Lewis GrossetPam HunlockThank you for listening each week. Join our Lewy Body Roller Coaster Podcast Facebook page.If you have a topic you would like us to discuss or wish to share your thoughts on any episode, please email us at:    [email protected] next week...Disclaimer: We are not medical personnel nor are we  offering medical advice. We are sharing our thoughts  and experiences with others to let everyone on this journey know they are not alone. Support the show

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On this episode and the next episode 17, its just Linda and Curry sharing some questions from support groups and responses from the many who continue to share ideas that will help us all through this journey with Lewy Body Dementia. The first two questions are geared more towards caregivers. We discuss how to respond to people who visit and then say that your loved one looks great or doesn't look like he has dementia. Do you ever get used to the diagnosis or used to what Lewy is doing t...

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Sharing between friends- things you might ask or want answers to

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This episode was published on December 16, 2020.

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