Dementia. Saying it out loud. Writing it on pretty
paper, typing it on a keyboard doesn’t make it any easier to deal with – my Mom
has it. Her Mother, my Grandmother, showed signs of it before she passed away
at 84. My Mom – turning 86 this year – is ‘neck-deep’ in the horrible disease.
I’ve known she had it for a couple of years – but convincing anyone in my
family was another story. Everyone just called it, ‘old age’. She
fell out of the bed, hit her head and it escalated everything.
My dad is still her caregiver – yet in a complete state of
denial. He’s of the philosophy if you don’t talk about it – don’t say it
out loud it really isn’t so.
I always had compassion and
sympathy for people that had parents with this disease – but until you walk the
path, until your own loved one has this – you have no idea what it is like.
My Mom’s lifestyle has greatly shifted. It’s at this
point – and I’m 55 years old—that I had the revelation that it was my Mom that
raised me. Took me to dance classes, took care of me when I was
sick. Made sure I had everything I needed on top of her holding down a
full time job. My dad ‘brought home the bacon’. And sat in a lazy boy- and
watched television. It was my mom that cleaned the house, planned and
prepared all meals, laundry, even planned what everyone wore. Now that
she is debilitated – you can’t even begin to imagine how things have dwindled.
I tried talking my father into getting help: Housekeeping help a
couple of days a week, food service to come in with meals, or even a sitter to
give him free time and my mother some company. I was vetoed on all
counts. Labelled bossy and controlling after I tried to persuade an
alliance with my brother, I threw in the towel and have had to sit back and let
things play out.
I used to talk with my Mom daily,
now I settle for once a week. I still write letters weekly, trying to put
photos in each and write of what my daughter calls ‘anchors’ or memories that
we shared to try and jar my mom into some facet of remembering who I am.
My Mom had always been so
healthy – she still has her tonsils, for God’s sake.
The hard part is knowing it
won’t get any better and there is nothing you can do and time only makes it
worse.
Her physician stepped in and mandated home health and housekeeping
come in and for that I’m truly thankful. Mom is not happy about it.
Dad doesn’t talk about it. But she’s barely getting the care she needs.
I have a plane ticket to go home to see her in a couple of weeks…
All I do is remember what it won’t be like when I get there. I recite
over and over again – ‘It’s not about you--- it’s not about you--- it’s not
about you’…. But I’m going to see someone who doesn’t know me, and a father and
brother who don’t want me there…. I kind of feel like it is all about me….
6 comments:
All so cruel....hugs...
Just leaving a (HUG).
wabbit4412@aol.com
I am so sorry...I see this a lot in the hospital, which seems to be a catalyst for it all. Many older people just don't want the intrusion of help, even though it is so sorely needed. My heart goes out to you...hugs!! It is so hard!
Much sympathy coming from me. My stepdad has Alzheimer's and my mom is his caregiver. I have told my sister how bad it is and to hopefully band together to encourage mom to either get more help, or place him in a nursing home. She came home last October and informed me I was exaggerating about how bad Jim is and that mom is doing fine. OY! So like you I am just letting things play out and it won't be pretty.
Sharon in Colorado
Please put on your mental armor. It's time to be the strong and bossy one. Don't give in and don't give up, she needs you. If need be, raise your voice and raise a fuss, she needs you. Make an appointment with the physicians ahead of time and confer with the doctor in person. Assemble any team members to be on your side. It sounds as if she needs a 24-hour care facility. We'll be praying for you and her. Do let us know how it goes.
It's so hard. My father suffered under Alzheimer's disease for 8 years.
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