This week I was pondering what would come next for the post. I had no idea. It seemed as though I hadn't enough time to settle my thoughts. And then I noticed something that was staring at me all along - technology!
I'm still reading the books, but I wanted to give my readers (Thank you, by the way! I'm incredibly humbled by the number of views this blog has had!) something that wasn't just words on a page; I needed something that spoke to them - and VOILA! I went looking for anything that could illuminate and stimulate us all - YouTube!
The following video(s) (I couldn't get them all in one launch - they didn't come that way and I'm not nearly talented enough to figure out how to glue them together - so your forgiveness, please) explain a goodly amount, and the speaker isn't dull.
I learnt a goodly amount from this, and pieces of the puzzle of Mom began to fall into place. Yes, I still have questions, and next week, when we see her doctor, I will be able to ask some; but I'm hoping that the referral for a neurologist (someone who deals with LBD patients and isn't trying to put something together last minute) pans out to answer more.
So, please, at your leisure, view the following. I hope this helps you understand and ask questions which will help guide this blog and us all to a better understanding.
I also need to give credit to the Lewy Body Dementia Association for their production (LBDAtv) of these videos. I may use more in the future for edification of us all!
Part One - Difficulties in Diagnosing Lewy Body Dementia
Part Two - Difficultines
Part Three
Part Four
Part Five
This has solidified many questions I had - Mom wants more salt - now I understand the need. There are other portions of this video (in its entirety) that help make sense out of this entire situation.
Until next time, Have a Wonderful Week!
Mom goes to the dentist tomorrow! Perhaps that will trigger something new!
I'm still reading the books, but I wanted to give my readers (Thank you, by the way! I'm incredibly humbled by the number of views this blog has had!) something that wasn't just words on a page; I needed something that spoke to them - and VOILA! I went looking for anything that could illuminate and stimulate us all - YouTube!
The following video(s) (I couldn't get them all in one launch - they didn't come that way and I'm not nearly talented enough to figure out how to glue them together - so your forgiveness, please) explain a goodly amount, and the speaker isn't dull.
I learnt a goodly amount from this, and pieces of the puzzle of Mom began to fall into place. Yes, I still have questions, and next week, when we see her doctor, I will be able to ask some; but I'm hoping that the referral for a neurologist (someone who deals with LBD patients and isn't trying to put something together last minute) pans out to answer more.
So, please, at your leisure, view the following. I hope this helps you understand and ask questions which will help guide this blog and us all to a better understanding.
I also need to give credit to the Lewy Body Dementia Association for their production (LBDAtv) of these videos. I may use more in the future for edification of us all!
Part One - Difficulties in Diagnosing Lewy Body Dementia
Part Two - Difficultines
This has solidified many questions I had - Mom wants more salt - now I understand the need. There are other portions of this video (in its entirety) that help make sense out of this entire situation.
Until next time, Have a Wonderful Week!
Mom goes to the dentist tomorrow! Perhaps that will trigger something new!
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