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    Posted May 15, 2014 by
    kmrdr
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    First Person: Your essays

    It Never Rained on My Parade

     

    The Alzheimer’s Association (alz.org) has named June “Alzheimer’s and Brain Awareness Month” to spread awareness of Alzheimer’s disease and dementia.

     

    My mother is only 64 and in the late stages of frontotemporal dementia (“FTD”), a rare disorder distinguished by its early onset and its impact on the behavior of those who are affected. The Association for Frontotemporal Degeneration describes the difficulties that FTD can present for family members:

     

    Behavioral changes are typically seen as changes in personality, emotional blunting or loss of empathy that result in increasingly inappropriate social behavior . . . . [T]he patient displays little insight into how inappropriate his or her behavior is, and little or no concern for its effect on other people, including family and friends.

     

    It is always hard to lose a parent, but certainly there are no pulled punches with FTD. Emotional blunting. Loss of empathy. Little or no concern for the impact of their behavior on other people, including family and friends. These aren’t descriptors that are pleasant to think of in conjunction with our parents.

     

    Sometimes it is hard to imagine that the person who currently inhabits my mother’s body is my mother. My mother wore beautiful scarves from second-hand stores. My mother, truth be told, completed most of my fourth grade science fair project. My mother canned thousands of jars of tomatoes. She loved her children. She was crazy about her grandchildren.

     

    This person changes the words of songs to include obscene words and sings them loudly on my brother’s front porch. When she lived with me for three months in 2013, her pet name for me was “slave” and we had many conversations about why she couldn’t hit me. This person called my daughter a “stupid loser.” She can be crude and mean and is largely unfazed by whether her actions hurt others.

     

    She can’t live with my brother. She can’t live with me. We tried both options and it was emotionally overwhelming, financially draining and harmful to our children. Our decision to move her to this facility was a good one; the right thing to do; the only reasonable step. But, still I sobbed when she asked me, “You aren’t going to leave me there, are you?” I just kept saying, “Mommy, we tried. We tried so hard. No one could have tried harder. We just don’t have any other choice.”

     

    And, yes, we were at the end of the line insofar as choices. But, even while my heart is torn in half, I am angry.

     

    I am angry because she always had a hard life.

     

    She got married when she was sixteen and endured many years of a physically abusive relationship. More than once before she took me to Girl Scouts or some other event, I helped her camouflage a black eye with make-up. I recently learned that head injury and trauma are associated with an increased risk of dementia. It is impossible to know if there is a specific link between her dementia and the years of abuse that she endured. Really, I don’t think I want to know.

     

    Regardless, she deserved more than this. She deserved to have the final chapter of her life filled with comfort and rainbows. But, as Clint Eastwood tells Gene Hackman in the movie Unforgiven “Deserve’s got nothin’ to do with it.” Clearly, Clint was right.

     

    I am angry because she had so much to give.

     

    She was a social worker in eastern Kentucky for many years. Then, she was the director of a domestic violence shelter in my hometown. Later, she worked with veterans in West Virginia and eastern Kentucky. She cared so much about “her veterans.” She would move mountains to help them receive benefits they were entitled to receive. I remember visiting her around Christmas and seeing the scores of gifts that they had brought to her: apple butter, homemade whiskey, woodcrafts. These gifts demonstrated the affection they felt for her because of her kindness and advocacy skills.

     

    I am angry because I didn’t figure out the extent of the problem sooner.

     

    I should have known something was wrong when, at 60, she was fired for poor performance from her job working with veterans. I should have known something was wrong when I saw emails with abusive language that she had sent to a friend.

     

    We knew something was wrong when she was in a car accident in December 2012. Thankfully, no one was hurt, but because she acted confused and combative, she was arrested for DUI (she rarely consumed alcohol and a urine test confirmed that she had not been drinking), resisting arrest and menacing. She couldn’t remember my brother’s phone number so she spent the night in jail. Because ignorance about dementia is prevalent in the criminal justice system, it will end up taking over a year and a half to establish that she is not competent to be tried on these charges. A year and a half. A year and a half to dismiss these charges when another Kentucky court found her completely incompetent in a guardianship proceeding.

     

    I am just angry. And I’m so very sad. And I wish I had my mother to comfort me.

     

    When we walked to my car to drive to the memory-care facility, it was raining. In addition to the other symptoms, my mother’s language is often childlike. She commented on the rain by saying, “You had better run to the car or it is going to rain on your parade.” I responded, “I think it already has rained on my parade.” She thought for a minute and then said, “I don’t think it ever rained on my parade.”

     

    I disagree. I think her parade was in the path of a tornado. But, it isn’t my opinion that matters. I hope she feels safe in her new home. I hope she finds a way to be happy. I hope she knows that we won’t forget about her. I hope she knows that we tried.

     

    (This essay originally appeared on the blog A Life Revised (www.aliferevised.com) and was also included on the Shriver Report's website.)

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