Harry’s Lantern on the Dementia Road
Tru here. Harry was leading the way as a Dementia Mentor when I arrived on this road.
Harry Urban February 1, 2015 at 7:14am
I want to go home, where I belong. I seem to be drifting away into this world of nothingness. I don’t belong here and can’t understand why I am here. These are …the thoughts that go through your mind when you suffer from some form of dementia.
You seem to suddenly realize that your life is being forgotten. You look around and don’t recognize anybody or where you are. It doesn’t seem right and you just want to go home. The problem is, I don’t remember where home is.
I may be at the point of no return. I can’t retrace my steps to that other life I once lived and I certainly can’t hide. I scream, I want to go home, but no one can reach into my mind to help me. I am alone and wandering down this road that I believe is going to lead me to a better life.

Harry Urban February 9, 2015 at 6:14am: Have you ever had the feeling that you helped someone you never met? There is nothing like it. I wish it would be a mandatory feeling that everyone had to feel at least once in their life. To me it is a very emotional feeling that is hard to explain. I never cry but I shed tears when I am able to help someone that has no one else to turn to. I call it my work but it is a gift given to me by this horrible disease I have called Alzheimer’s. Alzheimer’s has taken me to the darkest of places and I had to learn how to crawl out or be stuck there for as long as I live. It is not a social commitment or a part time endiver, it is what I am suppose to do with my life. I take it very serious and get upset when someone considers it nothing more then a place to talk. Unless you walk the path, you have no idea.
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Thank you Harry and Tru for shining the light from your lanterns for us all!
You are both in my thoughts and prayers.
Martha
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Thank you Martha 😀
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I only just found this when someone tweeted it to me. I’m so glad I did as it touches on some things I’ve been thinking about a lot recently, especially ‘Ttey want to remember us the way we used to be’. My dad died in December and I have lost count of the times people have told me to remember how he was before he got dementia. Why? He was still my dad. He may have behaved differently, may not have been able to do things as before, lost words and memories but the essence of my dad was always there at the core. I’m still thinking this through, may not be expressing it very well, but I feel if we pretend this disease has nto taken a hold we someone negate the person who has it. I’ll keep thinking until I know what I want to say but thank you for this post which has nudged me along a bit.
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😀 The same was true with my grandmother. Hope folks say the same about me. 😀 — Tru
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Thinking about this more, I very much appreciate how both my great grandmother then my grandmother handled their dementia symptoms. Their actions AFTER dementia are almost appreciated MORE than prior, because it showed their fortitude, creativity, love (despite confusion over not getting what they wanted, & even when not remembering WHO they were speaking with) and the growth of their unseen, spiritual relationships. They were why I created this poster for Dementia Mentors https://truthfulkindness.com/2014/08/13/new-poster-for-dementia-mentors/
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