Death Can Be A Process




“Remembering that I’ll be dead soon is the most important tool I’ve ever encountered to help me make the big choices in life. Because almost everything – all external expectations, all pride, all fear of embarrassment or failure – these things just fall away in the face of death, leaving only what is truly important.”

– Steve Jobs 

 


 

We all know that life is a process. 


I’m learning, yet again, that death can be a process as well.


I’ve been my father’s primary caregiver for the last ten years of my life. And in those ten years, people have told me that I’ve wiped enough of the buttock region and answered the same question over and over with the love and patience of a bloody saint to get me some sort of front-of-the-line pass. I definitely don’t disagree with them, although I’d prefer a front-row ticket to a rockin' concert instead.


Four of those ten years were full-time, full-on, full-everything.

Pops has dementia and let me tell ya, if you’re one of the lucky ones to not know or experience dementia, consider yourself—hashtag blessed—because that disease is a real dick.



Now, I could easily go on about how sad and scathing dementia is, but I won’t and one of the biggest reasons why I won’t do that is because we’ve actually had it pretty “easy” in terms of dementia, with dad.


He’s been happily living with this for ten years and when I say happy, I mean happy. The dude laughs his ass off constantly, rarely gets angry or agitated and is so easy to redirect.



It’s been almost six months since we transitioned dad into his new “home” (a State Veteran’s Home we absolutely love).


A “home” I judged others for placing their loved ones in until I hit my caregiving rock bottom and harshly realized I was slowly (and some days not so slowly), killing myself with exhaustion, adrenal fatigue and I could smell a wave of depression coming closer to my shore.


Not to mention the countless times I placed my marriage, husband and daughter on the back burner. Actually, I’m not sure I had any burners left because I blew those babies out a long time ago.



(Public Gratitude: Thank you, Husband—for sticking with me, our marriage and our family—I know I didn’t make it easy most of the time. Thank you for playing the long game when I could barely get up to bat at times. You forever have a free pass to make out with Scar Jo if that opportunity ever presents itself.)



Dad’s adjusted well to his new digs. Every time I visit him we laugh, tell dirty jokes as he flips people off and busts a gut and at the end of our time together I squeeze him hardcore, kiss him and tell him how much I love him and then leave him with a “Ciao for now!”.


Walking away and out of that building has gotten easier.

At first, I could barely walk out without feeling like I was broken inside, but I kept walking and waiving.

One step at a time and waiving to the nurses, knowing he’s in good hands.

 



We’re All Dying

Recently, The Vic’s health took a rapid decline, which took us all by surprise, because his health has been so stellar.


His heart is weak and his Alzheimer’s has progressed. In the last few months, more than once—as a large, Italian family—we’ve found ourselves next to The Vic’s bedside saying “goodbye” to him, clutching his hand while we listen to Luciano Pavarotti and Andrea Bocelli on blast and yes, laughing. Laughing because dad still hasn’t lost his sense of humor. Thank God.


And just when we think he won’t make it to next week, or even the next morning, he makes a comeback.

And my heart fucking stops.

I keep telling him that if his heart doesn’t give out, mine will in this perpetual I’m-Dying-I’m-Not-Dying process.


For reasons we sure as hell don’t know—but are no doubt grateful for—The Vic keeps making these comebacks from death’s door. Call it a surge, or hell, maybe he just wanted to rest, who the hell knows—he keeps rallying and living (sometimes better than he was before) to live another day.


We never know how long it will last, or if this is dad’s new normal, but we will take it.



All of this death stuff brought me right back to when I lost my mom to cancer at twenty-four years old.

Her death taught me to live and this up-and-down deathbed journey with my dad is turning out to be no different


Yes, life, we know is a journey. But, death—sometimes it’s not sudden, or overnight. Often, death can be a process as well.


Just like I watched cancer ravage my mom over a two-month period, death is having its own special way with my dad as well—like it does for all of us.



Because we’re all dying.

Maybe not right now, or tomorrow or in the next ten years.

But, we definitely know that we will die and with that thought, that knowing (as I’ve come to know too clearly)—can teach us how to live.



You see, I gave up a lot the last ten years to take care of The Vic.

I could say that I’m ten years behind in my career, or that my marriage was on the brink one too many times.


But, being on the other side of this caregiving expedition and holding vigil twice next to my father in the last two months, I can say with every cell of my body that I have not one regret and rode that part of my life hard and it was everything I needed to experience and then some.


And for that, my gratitude spills over.



Regret is a bitch if allowed to be. 


Death is a teacher if allowed to be. 


So, drop the bitch and pick up the teacher. 





Love + Deathbed Confessions, 

Keli


By Keli Conci 11 Jan, 2023
When Gracie Comes A Knockin' I'm not a great patient. I'm really not. So when my Hubs nervously says to me, "I think you have a brain tumor," I laugh. Hysterically busting a gut in his gorgeous, blue-eyed face. "A what?!" I shockingly remarked as I lay in bed for the 3rd week straight from what I thought was an ongoing "pressure" headache. A very long "pressure" headache that happened to a woman who rarely ever had so much as a "regular" headache in her entire life. I thought my Hubs was talking gibberish. Brain tumor. Hilarious. How could a healthy 39-year-old woman such as myself have a brain tumor? Preposterous, I say! Do you have a brain tumor, sir? Looking back, however, I can kind of understand where he was coming from. Ever since Christmas (which I didn't attend because of this "pressure" headache), I wasn't myself. For the next week or two I was self/or friend diagnosed with either vertigo, sinus congestion, and some other oddities I won't even mention. I thought I could "tough" my way through it; I'll get better. This is ridiculous, I thought, to still be suffering from some crazy-ass head thing. It wasn't until I was going into week 3 that I got concerned: I wasn't better; I was fucking worse. Like way worse. So much more worse. I couldn't sleep at night and I recall telling my Hubs, "My head hurts so bad I think I'd feel better if I blew my brains out." That's how in pain I was. The pain got so gnarly I notified my Hubs that we have to go to an Urgent Care pronto. I could barely sleep, all the OTC medicine I was taking wasn't working anymore, the holistic concoctions and potions weren't even touching my pain and any light felt like my eyeballs were being stabbed by tiny daggers. As I lay on the Urgent Care table, with my eyes closed due to the piercing brightness, I spewed my symptoms to the nurse and doctor. Eventually, the doctor told me my labs showed I had a UTI. "A UTI!" I screamed in my head. You've got to be kidding me. I know my body and this isn't a UTI. Apparently, I wore that same expression on my face because she quickly responded. Doc said I'd be shocked at what a UTI can do to the body. I laughed her off and wanted to believe her, but knew something deeper was going on and a UTI wasn't the answer. We were sent home with a sympathetic look, a prescription for antibiotics, and a "check-up with your doctor, sweetie" send-off. The days that followed only got more painful; more dreadful. Four days later—by Thursday afternoon—I began puking. And that is the last thing I recall. Let's name this the fade-to-black scene, mmmmkkkay? The puking scared me, but it also scared the shit out of my Hubs. He had been wanting me to go to the hospital and I stubbornly refused (like I said I'm not a great patient)...over and over and over again. I was incoherent and unable to make any decisions at that time. The Hubs tried his best to get me hydrated and ready to take me to the ER. At that point, I was no longer able to tell him, "no". When he called our neighbor to help him heave-hoe me in the car for the ER (I was like a sack of 120-pound potatoes), I began having a seizure. Our neighbor was there at that moment and told Hubs this just turned into a 911 emergency as he called for help. The paramedics arrived; I was assessed, stabilized, and then taken to the ER via ambulance. At the local hospital, they found a brain anomaly. I was then sent via flight-for-life to another hospital and underwent a 5-and-1/2-hour brain surgery to remove all of (what we came to know) a 6-centimeter (think egg-size) Grade IV Glioblastoma brain cancer tumor (whom I affectionately call "Gracie"). Yep, when I do things, I do them big. That whoppin' glioblastoma was in my left frontal lobe and had amassed such a large field in my brain that when it shifted to the midline of my brain (or something along those lines), that's when I had a seizure (and also when a part of my right peripheral visual field was cut off). The tumor was a honker and clearly explained everything I had been experiencing physically—up to that moment. Turns out, this almost 39-year-old "healthy" chick, indeed, had a brain tumor. The Hubs was absolutely right, damn it. Medical Turban *Photo heads up! There are two pictures coming up that show my incision from my surgery. If that doesn't float well with you—please skip this part.* If my last memory was puking, when did I wake up from my own abyss? 27+ hours later to be exact. At that moment, I felt my eyeballs squinting as I noticed I was in an ICU bed and feeling what I like to call a "medical turban" wrapped around my gourd as medical professionals walk by in shock that I'm awake. My head feels like a soft pillow. Is this some kind of weird heaven, I ponder? God sure is hilarious if he has a hospital up in the sky. Turns out, it was Earth. And my head felt so much better. Hence the medical turban.
By Keli Conci 07 Jan, 2020
Grief⏤The Ultimate Permission Giver I thought I was losing my mind after my Pop’s died . No joke. I began to think the dementia that finally ravaged his brain, was about to do the same to mine. I couldn’t think straight, literally. My short-term memory was shot. Which sent me down the Google rabbit hole where I found helpful articles that explain how grief is not just processed emotionally and spiritually; it’s processed physically as well . Lightbulb moment; that makes total fucking sense, I thought! I didn’t question my sanity after that. Instead, I got really intentional about taking care of myself and my grief. Post-Physical Grief Revelation What unfolded after that has been interesting because grief became the ultimate permission-giver to say “no”. Because grief left me feeling depleted of almost everything⏤mentally, emotionally, spiritually and physically⏤I gave zero f*cks in life. With not much left in my tank⏤if you’re not my husband, daughter, or client⏤I rarely have anything left over to give. Protecting my energy has become a full-time job. It’s made me say “no” to just about everything outside of my family, house and work. It’s made me say “yes” to everything that helps my world feel, well, soft and not so dreary. And, damn, it feels so good. Which makes me question... Why did grief have to give me the permission to say “no” to whatever I wanted to say “no” to? Why couldn’t I have those boundaries without having to lose my favorite person in the whole world? Grief⏤The Ultimate Permission Giver So, what does that actually look like? You know, saying “no” when you want to and saying “yes” when you want to. Being all congruent and aligned in life. If it’s hard for you to place boundaries or say “no” when all you do is say “yes”⏤here are some examples of how I laid the grief/boundary smackdown. Listen to your body. Bloody hell, if you’re tired, be tired. Your grief body needs all the help it can get. Reschedule, cancel, leave the party, get in bed while the sun’s still up to tend to your tired. I went to Scottsdale, AZ for a business trip and stayed in this magnificent, swanky-ass resort. After the conference, I passed out at 6:30pm and never really took in the beautiful place we were in. That’s more than okay. I woke up refreshed and my body and brain were happy I did just that. Be brutally honest with yourself and others. Now that I know tending to my grief-self is #1 priority for me, I have very uncomfortable conversations with family, friends and even strangers. I decline gatherings and invitations constantly (including holidays, birthdays and celebrations), or give the caveat I may not stay too long and tell people up front: In my grief process, currently, I get overwhelmed super easily, so if I do come to your shindig, don’t be surprised if I leave early. I’ve ordered the wrong milk in a café and told the barista, “Sorry, my dad died recently and I’m completely out of it.” When my family or close friends ask how I’m doing, my usual response is, “I’m here. You know, just feeling like my left arm is cut off and I don’t know where it is.” The pre-grief Keli was a jovial little bitch and her remarks would have been, “Great!! How are you?” Grief and death are subjects people can get squirrely with. My honest response is to honor my journey…whether that makes you comfortable or not. And of course, I think these topics should be discussed more in life because they can be lonely and isolating if you don’t talk about them. I fumble constantly but give myself GRACE. Here’s where I fumble⏤when I think I can say “yes” to something (in the moment) but when the time comes, I actually don’t have it in me to do the thing I said “yes” to. I’ve had to say “no” at the last minute to my very best friend more times in the last couple of months than I ever have in our lifelong friendship. I forget to tell people the stipulation: “This sounds like a 'yes' to me right now, but let’s revisit this when the time gets closer.” In December alone⏤the month of my Pop’s and Hub’s birthday, along with the holidays⏤we ate out constantly. Not something we do consistently, but I gave myself grace to not cook and get through this hectic month as sane as possible. So, perhaps, if you blow at boundaries, or want to get more aligned with how you show up in the world and where you place your energy⏤ don’t wait for grief to give you permission⏤do it now, yo! And get to flexin’ those boundary muscles. Love + Big-Ass Boundary Grief Lessons, Keli Psst…Grief-life is a giant mirror for your friendships and relationships in life. It’s a brutal process to watch someone grieve. It’s also a beautiful process to be in the thick of it with them. Also, if you don’t have a robe (it’s like you’re constantly wearing a warm hug), get yo’ass to a Target ASAP. I basically live in this wardrobe now.
By Keli Conci 05 Sep, 2019
It's Never Goodbye, It's Only So Long  My pops… The guy I talk (write) about all the time. The dude who I said has the number one spot in my heart (even my hubs knew his ranking). The man whose humor surpasses any comedian I’ve ever watched. And who rocked a raging case of CRS/Alzheimer’s like no other… Went tits up recently (Vic’s words for anyone who died was “tits up!”). I had the privilege of honoring who he was in life and writing his obituary, which I knew could have absolutely NO pretense in or around it! Here’s to The Vic, my pops, for showing me how to live a life with just enough grace, heaping compassion and a fuck-ton of laughter.
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