The Continuing Education of the “New Normal”

The two hour drive from D.C. to Berkeley Springs gives me time to build my courage on the way there. I give myself a pep talks. Visits are difficult. They are incredibly emotional. Mom’s disease has stolen her, and I struggle with it at times.

Every mom visit is something new. She is talking less. She is less steady on her feet. She engages in eye contact in shorter intervals and keeps her head down. I consider this the continuing education of dementia.

Dementia is a horribly cruel disease. An easy fact to comprehend, and an excruciating fact to live.

Part of this education is physical and mental and learning the ever-changing capabilities of my mother. They seem to ebb and flow, continually decreasing little by little. These new levels of decline are what we call the new normal.

Part of this education is emotional and learning to accept watching your mother slowly disappear before your eyes. She lost her ability to engage in conversation, to feed herself, etc…. I remind myself of this to and from Berkeley Springs every visit. I am rational. I know this will never get better. I accept that. Doesn’t make it any less difficult.

Sunday’s visit was a new normal. Sitting down in the chair beside her wheelchair I smile and offer my ceremonial “Hi Mom!”

She stared at me for a little bit. It felt like a long stare. Silence feels heavy in those moments.

“Hi Mom.” Her response came out muffled and slightly slurred.

“I’m not Mom. What’s my name?” I am trying to keep smiling and sound upbeat.

She stared at me for a while. Her eyes are beautifully expressive. She stared and said nothing. She genuinely didn’t know who I was.

This didn’t feel like a temporary slip of the memory. She has confused me with someone before. I was Billy for a while.

There was a chunk of time after I came home from Liberia that she called me Billy. It lasted a few months. She had a brother named Billy. We’re both tall. Had beards. Handsome with charming smiles. I was Billy for a while but that passed and I became Joey again.

“I’m not Mom. What’s my name?” My second, third, fourth, and fifth attempt over the next hour come out flat, and like a whisper.

She’ll stare at me for about 30 seconds to a few minutes, then eventually lose interest and look away.

Over the next 45 minutes we periodically look at pictures of Matt and me, playing the game of pointing and asking “Who’s this?”

Matt is identified each time. With me there is silence. She stares at me, deeply, then looks away as if the question times out.

She has struggled to remember my name for about a two months. After a while she rattles it off. No harm no foul, and I think nothing of it. This, however, is different. She has no idea who I am.

The two hour drive from Berkeley Springs to DC gives the time to continue my emotional education on the way home. There is a new normal. I’m not her Joey DeMarco anymore. I’m not even Billy. I have become the polite stranger that comes to visit. I wasn’t ready for this part yet.

Matt is now the last man standing.

Happy Halloween

A few pics with mom and the most adorable little pumpkin around!

I’ve taken a hiatus from the blog since summer to pack up and move. (More on that in a future post.) Happy to be back.

Thanks for keeping the good vibes coming our way! Happy Halloween.

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Boob Job

My friend Mike complimented me a couple of years ago saying I was able to follow two or three conversations happening around me at the same time. I credit it to being a trainer and having to pay attention to a room full of people working at different speeds. And I’m sure that’s part of it. Sometimes when I’m with mom I wonder if it’s partly
the way I’m wired biologically.

Even though my mom doesn’t initiate or really have many conversations anymore, it doesn’t mean she’s not constantly listening to everything that’s going on around her. She’ll turn her head when she hears something down the hall. She’ll repeat a word or phrase that’s said on TV. She’ll even pick up and repeat the pages over the loudspeaker.

Though we don’t have conversations, mom is still listening when we talk. She’s still paying attention. A nursing home is a busy and loud place, with lots of simultaneous conversations, equipment beeping, TVs playing, and visitors in and out. She’s takes it all in.

Yesterday when Joey was telling me a story that involves a getting a “boob job,” mom picked right up on it and wouldn’t stop repeating the phase…

Undeniable likeness of Helen

My coworker asked me this morning if I had any new pictures of baby Eliza.  While I thumbed through photos on the iPad my coworker asked, “Do you have any baby pictures of your mother?  I mean, I see you in Eliza, but does she look like your mother or father too?” 

 I’d never thought of that question.

When Eliza was weeks old Katie and I held up her photo beside my baby photo from around that age.  The resemblance was uncanny…and a little flattering to me, not so much to Katie. 

Looking at my Mom’s childhood picture I can see her in Eliza.  They have the same eyes, and nose.  They share similar smiles.  Looking at Eliza, you can see that the “Power of Helen is strong with this one.” 

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It is moments and discoveries like this I know my Mom would love to consciously be part of.  She would have a fun laugh comparing pictures like this.  The sad reality is in the near future these two women will not remember each other.  Eliza Helen met Helen Katherine too early, and Helen Katherine met Eliza Helen too late.  As Eliza gets older my mother will be a memory, a spirit haunting picture frames, existing as lore told in stories by Matt, Katie and me.  However, it is comforting to know they will share more than their name.  

Eliza, I believe, will grow up to be headstrong, kind, stubborn, able, compassionate, patient, determined, and have an unwavering sense of family.  Some of these traits she will get from Katie and me.  If you ever wonder where she gets the rest of her character just look her in the eyes, and remember she is a Helen.    

Lights, Baskets, and Sunshine

Music and singing were always a part of mom’s life. And they continue to be a way we track the progression of the disease. It’s been a while since I posted some singing clips. Here are two short ones…plus a bonus reprise from the toilet! (Oh yeah, we sing there too!)

This little light of mine…

You are my sunshine…

A reprise from the toilet…