I am still working on my theme How to Face Fear with Knowledge. It requires research. It has to do with the professional community surrounding Alzheimer's World trying to categorize the class they assign to it in a workable definition to aid research in finding the cure. The more they can define what Alzheimer's Disease is not the more quickly they can refine the disease for research making it have less triggers that start or exacerbate it. This is helpful in finding the cure but does not do a damn thing for the person who has Dementia that does not fit in.
If the shoe doesn't fit you are screwed. Only Cinderella need apply!
Can You See ME?
I am sitting here with
my eyes open, though you speak as if I am not here.
I am here! Can't you
see me?
I AM still in here!
Touch me with your
hand, Please, my skin still feels. Rub my arm and pat my hand. I CAN feel you.
I long for human contact.
I AM in here.
Talk to me. I am alone
and isolated in this chair. I am lonely but I cannot tell you. I feel helpless,
I can't move by myself.
I sit here all day
with no stimulation, only the sound of alarms and intercoms.
I am bored! PLEASE
TALK TO ME!
This poem was written by Anne Marie a woman suffering from dementia. The poem was sent to us by Judy Berry, Lakeview Ranch.
Can You See ME
Read the poem “Can
You See ME?” then tell me why! Why is Alzheimer’s Disease (AD) treated like
leprosy and those of us with it shunned like lepers? This poem tells it like
it is.
Is there an answer for this? Is there any reason why?
We have allowed sensationalism to be made of our disease, trusted
others to make it's shock value such as to get response. That response is
contribution of money to find the cure. The shock value is intended to create
fear; afraid you might get AD if it you do not contribute and make it go away.
In this way we are used and abused for no good coming to us. Only
the ones getting a financial return from raising money are getting a return on
this characterization.
We are the losers in the poem. We are the losers because there is
no hope. We get the disease; we are placed on the shelf where there is no
notice of us, no programs to help us maintain our functionality in the Early
Stage. When it is time for the “Home” nothing is done to keep the institutional
cost within reason.
Why? There is nothing that can be done but to keep us safe and
then be committed to the institution when this is no longer possible. This is
what Dr Alois Alzheimer said in 1902. This is what too many professionals think
and sat today.
Because of the fear of it as it is increases in number then
melodramatically characterized as even worse no one wants to be in the same
room with an untouchable.



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