Page 29 - Keralite Magazine _2020
P. 29

KERALITE      APRIL 20 20    35
          At her follow up appointment with the neurologist,    The worst thing about neuro-disorders, such as
          my mother was asked how she was doing.  She said,     dementia,  is  isolation.  Due  to  the  stigma,  families
          “My family, they are my eyes and my memory. As        su er in silence. Dementia is viewed as a family
          long as they are with me, I am neither blind nor      secret. One that must be kept hidden from the
          forgetful.”                                           community. This is especially true in the Indian
                                                                community, where illnesses like these are perceived
          That was an “ah-ha” moment for me.  Her positivity
          in the face of this dreadful disorder blew my mind.    as a source of shame. There is more concern about
          I shifted my focus from curing to caring.             what people might think or say, than about the
                                                                people who are su ering. This leads to social
          My mom has the most beautiful eyes. I had to be her   isolation and decreased quality of life. This
          eyes. I needed to do what I could to fulfill my        avoidance of talking about it does not help anyone.
          mother’s dreams.                                      There is still a person behind that mask of dementia
                                                                who needs love and support. Falling sick is nothing
          My mom wanted to travel, so I travel.
                                                                to be ashamed of.
          My mom dreamt of doing community service, so I
          serve.                                                We  can  help  each  other  by  responding  with
                                                                a ection and reassurance; o er an outing, call the
          My mom loved to dance, so I dance                     caregiver, bring food over, drop by to say, “hello.”

          I have the privilege of being her eyes.               The  humble  advice  I  can give as  a doctor  and a

          Too often, dementia cripples families and friends.    daughter to those impacted by dementia is to focus
          We  don’t  know  what  to  do,  so  we  do  nothing.    on joy.  Spend time with the person you love; visit,
          Rather than trying to understand life with dementia,   hug,  laugh, tell  stories.  It is  an emotional journey,
          we fear it.  We forget that while caregivers su er, so   but everything doesn’t have to be so serious. So my
          do the loved ones with the disease. Each day is a     mom forgets, repeats herself, talks out of turn, and
          battle;  fraught with a manic-like depression going   that’s OK. She is still with us and we will continue to
          from highs to lows.                                   be her beautiful big brown eyes.


                                                                To learn how you can help, go to caregiver.org or
                                                                listen to the Beaumont Housecall Podcast: Caring
                                                                for Aging Parents episode.
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