Lewy Body Dementia Awareness
Posted on : 16-08-2010 | By : Cathy | In : Uncategorized
5
I can trace back about eight years, the signs my dad has been showing of Lewy Body Dementia. It seems to that for a long time, they did not know exactly what his diagnosis was, and although they may have mentioned the words Lewy Body, perhaps, I was not ready to hear them. Either way, I feel like I came late to the party with understanding what was happening to my father. Although, I’m not sure that treatment for him would have resulted in anything other than what we’ve done so far, I feel that “treatment” for me and for the family would have been different. (Maybe)
For the last few years, there’s been a coming to terms with wanting things to be different than they are. There’s been a coming to terms with “he must” or “I must” be doing something wrong – otherwise why would he be this way? There’s been a coming to terms (for me) with how each member of our family has responded to my father’s illness.
And the place where I’ve been able to find peace is in asking these questions:
- What beauty and lesson does this moment hold?
- What are the gifts that are available to me through this moment?
- What am I to learn from all of this?
As I ask myself these questions, I begin to allow myself to see the gift that my father is to me and I smile knowing that he has never stopped teaching me and offering wisdom, while patiently waiting for me to be able to see…
Please click on the logo for more information about Lewy Body Dementia and help spread the word!
Knowing the signs and symptoms offered me a chance to see beyond the behaviors and interact with the person behind the label of Lewy Body Dementia, creating a relationship based on love and compassion, rather than a relationship based on the personality with these symptoms.
.



Log-In For Coaching Resources
Lewy Body Dementia Awareness…
I found your entry interesting do I’ve added a Trackback to it on my weblog
…
My Dad is in the early stages of LBD but was already misdiagnosed with Parkinsons. I have been researching like crazy, crying lots and trying to determine how best to support my Mom. Your three questions are perfect and I will laser them into my brain so as to get the most out whatever time is left with my Dad. Thank you.
Hi Heather,
I’m glad you found the questions helpful. I spent a long time focused on what I was losing until I decided to look at what was available for me to receive. Knowing the symptoms made it much easier for me to live within that framework, rather than desperately trying to have my father be something other than what he was. I was able to enjoy our time together more.
Cathy
My dad is in the final stages of his LBD. His initial dx was Parkinsons, when the family mentioned LBD it was dismissed. The Parkinsons medications gave him severe hallucinations, the doctors then said dementia. It has been so frustrating.
We had never even heard of LBD and I feel like we were led to believe, that there was nothing wrong, just a cute old man being a bit eccentric. I’m sorry to hear about the medication, it can be confusing and so frustrating not knowing what do to or how to help.