Wandering Lite with Lewy Body Dementia
Getting to Acceptance

Stage 1 – Knowledge about LBD


It is important to do it together with loved ones so they learn too

Prior to receiving my diagnosis, my doctor had identified that there were three types of dementia that he suspected with my condition.  After considerable testing the diagnosis from my doctor that I had Lewy body dementia.  I have course wanted to know more about it, the doctor disgusted with me, and of course I had many questions so he asked me to put them down and he would be more than happy to respond to with either answers or resources.

This started me on my journey of understanding Lewy body dementia last February 2020.  The more I read, the sadder I got. Lewy body dementia is one of the most aggressive types of dementia. Because it is so progressive that a timeframe is predictable.

What’s not predictable is how long you retain mental capacities. The brain has a magnificent ability to repair itself, but it would appear so much damage. The kind of good news is that people with higher mental capacity seem to hold out a bit longer. I learned in the year, as the Robin William’s story came out that battling with this disease takes its toll.

Because I gave myself time to understand the disease, and Dr. McDonald at Cleveland clinic was kind enough to help me with honest answers from the start. I was able to come to grips with a good knowledge base.


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