Blood From A Stone

When Philip first died I thought, what could ever bother me again? What could ever be so bad that I would care that much, as long it wasn’t about Natalie? I saw his death as the second worst thing that could ever happen to me, as the first would be to lose both my children. 

Ten years on and things do bother me. Writing is my attempt to keep them in perspective, writing today is just to vent because the post I’ve been working on is so difficult to unravel I am starting to lose my shit. How to examine life with my family, something I’ve not taken a good, close look at? Not just my growing-up-with family, or my married-with-kids family, but my large, extended family, too. I’ve kept a distance from them since I was old enough to move out on my own at 22. I’d see them at family occasions but was never one to reach out. On my mom’s side were six brothers, most of whom married, some of whom had kids. On my dad’s side were two sisters, but they wound up moving to different states and since my mom didn’t much like his family and she ruled the roost, my focus has always been on her side.

I didn’t even much keep in touch with Maria, my sister-cousin. I never made a conscious decision about my family one way or another. I was absorbed in my own life and my family was on the periphery. I didn’t like my parents, loved my aunts, uncles and cousins but felt different from all of them. Plus – and this is something I don’t yet understand about myself – I don’t maintain bonds with people. I have no friends from childhood, was unable to stay married. I make friends here and there, invariably let them fall away. I shy away from people in general, I spend a lot of time alone. My children are the exception. 

I come from a loud, funny, boisterous Italian family who got together every Sunday for dinner. Might sound like a minor point, but since my mom is the only female out of seven children, once she married her last name changed which meant my last name was different from the rest of the family and when I was old enough to realize that I added it to my list of resentments as well as the list of Why I Am Different From Them. I put myself in a double bind – I resented my immediate family for what they couldn’t give me and was desperate but unable to feel part of my extended family. I didn’t blame them. It was my fault. They were uninhibited, I was self-conscious. I wasn’t funny the way they were. I was withdrawn and uncomfortable and had a book with me wherever I went. I once heard an aunt remark, “Look at her. She forgot her book so she’s reading the TV Guide.” I don’t know how she meant it, but I took as some kind of slur against me.

I did not come from a family of readers – the only one who read was my dad and I looked down my nose at him as he read what I considered cheap, easy-read paperbacks. Were they? I don’t know. What I do know is I was a sensitive, precocious kid, possessed an intelligence neither of my parents had, was exceptionally bright in school. I clung to that intelligence because it was all I had, at the same time feeling ashamed of it as it was something that yet again kept me apart from my family. No one in my family went to college and that was the track I was on. My dad’s reading was inconvenient for me because I wanted to be nothing like him so I had to write it off as inconsequential. I might have felt sorry for myself for feeling like an outsider, but I also cherished it. 

And I started drinking when I was 11 because it was just too much to deal with.

I do not want to get into politics in this blog. It’s too painful. I used to follow the news avidly until Philip died. I felt flayed by his death and anything contentious was like sticking burning brands into my already tattered flesh. It was all beside the point. I am bringing it up now to make starkly clear the differences between me and my family. They are all rabid Trump fans. As in Michael-Savage-believing, Alex-Jones-listening, January 6th was no-big-deal-excusing, Trump-can-do-no-wrong affirming, MAGA-flag-flying Republicans. I am not. 

That screams volumes about the differences in the ways my family and I approach life. Inherent in that is a wound that won’t heal. I’ve never asked myself what it is I want from my family. Love, of course. But I can’t say that they don’t love me…I want to be seen. There. That’s what it is. I am not seen by them and having said that, it is way past time to let it go. Blood from a stone and all.

 I have felt guilty for not keeping in touch with them, particularly aunts and uncles. But that guilt was born from realizing Maria does keep in touch them, always did. At this point in our lives we are down to two aunts and two uncles, but she invites them to her home, makes plans to go out for lunch or dinner with them, calls them regularly, has group texts going that even include my brother. I don’t even know what I would say to them if I called, and to be fair, I know those group texts are Trump-related so why would I be included in them anyway?

Recent interactions with my two uncles (my mother’s two remaining brothers) regarding my mother’s Alzheimer’s and her financial state have shown me who these men are as well as helped me understand why I do not and cannot consider them the kind of family I can turn to. I’ll be going into greater detail about this as I write more about my mom and Alzheimer’s . But since I started working for Maria’s husband two years ago (he’s a doctor, I’m the office manager), since I’ve been coming down to the shore and spending more time with her these last three years, and since my mom developed Alzheimer’s, I’ve been forced into family dynamics in a way I have never been. I am seeing real, adult reasons why I can’t have the intimacy I imagine other families have, not childish projections of being not only unloved but disliked by them because I am just not enough. And as usual, while I am very good at seeing the why’s of the thing being unattainable, I am not well-versed in the how’s of getting what I want. I’d do well to first consider what that is.

© 2022 Denise Smyth

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What it Takes?

I started this blog a year after Philip died. I was as raw as I’d ever been – no, more raw then I’d ever been. I spent years trying to put words on what I felt like. There was no other way to survive. I wrote that there weren’t words to describe what I was feeling because the usual words – grief, despair, agony, etc. – were words I’d used before and what I was feeling was beyond any of that. So I strung words together best I could and made whatever sense I could.

Over the years, grief’s hold on me lessened, old habits of depression felt normal, life felt hard and unmanageable. Writing no longer interested me, quilting did. That’s where my creativity took me for a few years until I lost interest in that, too. I’d write posts here and there but not much else. I started watching a lot of TV and just didn’t care too much about anything except Natalie. A couple years ago, as I mentioned in my last, I started reading about the Tudors. Kings and queens fascinate me, Game of Thrones had ended, reading finally gripped me the way it did when I was younger and would not go anywhere without a book. I still watch TV here and there but it’s reading that I’m mostly caught up in.

Still, not much creative output. It just seemed easier to let it all go and wait. For what? I’ll leave it there for now.

I am at the Jersey Shore at my cousin Maria’s house and will be here until Labor Day. So much to say about this, but not now. When I’m here I usually go for a walk first thing in the morning, around 6:30 or so. When I’m back I make coffee and sit outside to drink it. Her house is on the bay, her backyard spa-like. There are multiple places to sit or lounge, a dock with her boat and jet-skis, a pool and a jacuzzi and her big, beautiful, long-haired German Shepard to keep me company. Last night he slept with me, the only male I’ve had in my bed for a decade.

When I sat taking it all in this morning my mind was going its un-merry way. I’m 64 now, and I can say that physically I’ve had a good 63 years but things have started going wrong and I hate it. How unfair, I was thinking, that we are born into bodies that take up way too much time distracting us from what really matters, yet distract us they do. Whether we’re young and insist on basing success upon physicality or older and doing the same but with the bitterness of our aches and pains, what’s the fucking point if we have to constantly deal with our bodies?

Somehow, I caught myself. Is this what I want to be thinking about? Am I even thinking, or is this just mind-meandering, an updated version of former, similar unhappiness? And I remembered earlier years of writing this blog, when I certainly had a lot to be unhappy about. But there was a quality there that stood in sharp contrast to what I’d just been doing. Of course I was inconsolably, desperately, unhappy. But I was somehow with it, open to it, and willing to put words on it. It was not work to do so. I was too devastated by Philip’s death to be anything else.

For years I have been unable to be in that place. It’d been suggested to me I was having a “dark night of the soul,” that I would come out of it. Just words, I thought, because it’s been years of it. A matter of will? How does one will oneself to care? I don’t know how to explain how I got there any more than I know how to explain why today I’m able to sit with this, why or how I’ve been able to write these last few posts. I coast along, not forcing a particular direction. That’s what I’ve been feeling like for years and not caring to do otherwise. I’m not saying I’ve made a big change, some willful decision, but – for this moment, at least – I am wanting to think about what is going on. With me and Maria, my mom and Alzheimer’s, my extended family, my addictions, my solitude and most of all, my children.

There’s one change I want to note. In my early 40s I decided to go on antidepressants. I’d been in therapy for 20 years at that point, sober for about 17 and still depressed. I’d had several therapists suggest medication but I’d wanted to get to the bottom of my misery without chemicals. Finally I thought, “what the hell” and started seeing a psychiatrist. That led to over 20 years of trying this med and that med and settling on Wellbutrin for about 14 years. At some point that wasn’t working, so my doctor tried adding this other med and that other med and when, in 2010, I had a meltdown, my mood-managers got together and decided an anti-anxiety medicine was in order. By then I was hooked on thinking some kind of drug has to help me and when I was prescribed Gabapentin I thought I hit the jackpot.

Gabapentin made me feel good about being alive. It was not subtle, like an anti-depressant. Its effects could be felt within a short time of taking it. But I am an addict. So if a bit of something shifts my mood enough that I feel good about being alive, then more of it must make me feel even better about being alive.  It was prescribed, so it was okay. I managed to get my initial dose raised about as high as it could be, then started taking none on one day so I could take extra another day. I talked about this to no one. Eventually Gabapentin worked against me. I was irritable, forgetful and nervous and fearful of everything. I was also trapped because I saw no way to stop taking it. 

Except I did. I’m not sure when except that it was months and months ago. Sometimes I wish I paid more attention – if you know anything about AA, anniversaries are a deal. People might say, “the person who woke up the earliest is the one with the most sobriety” but I believe few really feel that way. I was as caught up in year count as anyone else – had I not started drinking when Philip died, next year would’ve been 40 years, people would’ve admired me and I’d have eaten it up. But I also know the emptiness of that – needing that kind of recognition and approval does not fill the hole that demands it.

I still see no clear cut path as to how I was able to stop using something I swore I couldn’t live without. If I’d asked for help – as I did when I went to AA  – then the steps would be obvious. But this I did mostly by myself. I began to ask Philip to help me as – and again, I will not get into this now – he is very much with me and it is he who I turn to for help every day. Between the two of us I managed to stop by tapering off. I did not involve my psychiatrist. The only medical professional I turned to was S, the Physician’s Assistant who works in my office and who is my practitioner. When I was down to taking the bare minimum before actually, finally stopping it altogether, I was not feeling well. Not emotionally or mentally, but physically. Weak, tired, fatigued – not the kind of symptoms I could find while trolling the internet for “Gabapentin Withdrawal.” My PA suggested I might need to stay on one or two pills a day. I refused. The weeks went on, the symptoms went away. It was over.

Next went Abilify, which was supposed to enhance Wellbulltrin. That was easy, I did not feel any different. And finally, Wellbutrin. For both of these I spoke to my psychiatrist as to how best to taper off. I am well aware one does not just stop taking antidepressants on a whim. I received my instructions, bid her good-bye, told my PA what I was doing and that if I needed her, I’d let her know.

I am now off all of it, and have had no repercussions. I tapered off the Wellbutrin more quickly than advised because through each stage I had no adverse reactions and because sometimes I know my own body better than somebody else. Again – I wish I kept track of when I did it, again I can say it was sometime this year. So I’ll leave it that 2022 was the year I stopped taking prescription medication designed to make me emotionally and mentally “better.”

I’ve written all this because I assume it is an aspect of why I have the ability I’d believed I’d lost to sit and think about the life I experience. And for all the decades of trying to deal with my life through alcohol and drugs, both legal and illegal, the only organic way I have of doing that, of attempting to take myself seriously and at least try to find meaning, is writing. And that requires removing whatever blocks my process.

NB – This is my story, my experience of working with a psychiatrist and the medications I was prescribed. It is no one else’s and I am certainly not recommending anyone flush their medications down the toilet. I am not a doctor, I have not even done any amateur research into this topic. I do know there are levels of depression and psychosis and when someone needs help, my only suggestion would be to find a doctor you trust to help. I consider myself fortunate that I was able to leave behind Wellbutrin so easily. And whatever I’m going through now is not something medication, prescribed or otherwise, can “cure.”

© 2022 Denise Smyth

Surface Dive

Self-centeredness, self-pity. Traits, I’m told, of the alcoholic. Traits, I say, of humans. But in the context of addiction, the work is to learn to live sober and these are two of the things to pay honest attention to on the road to recovery.

Note – it might be prudent to explain my mother’s current condition. She is fairly healthy for 90, on two medications for her memory and one for high blood pressure. She can, with difficulty, get up and down the stairs on her own, can bathe and use the bathroom on her own. She dresses herself. She is no longer allowed to drive, which is causing her great angst. She remembers things from long ago but forgets what happened two minutes ago. I have called her within a few minutes of someone else calling her and she does not remember talking to that other person. She will often call me after I’ve spoken to her to ask if I just called and what we talked about. She repeats the same questions over and over during conversations and repeats the same sentences no matter how many times you call or how often you speak to her. She is irritable. She is at a point in this disease where it is not clear what she needs, but it is clear she should have even a few hours of daily company which is why we’ve hired someone.

I am going to start by indulging in self-centeredness. My mom’s Alzheimer’s might not be about me but that’s how I come at it. My behavior does not reflect this. My rage does. I call my mom regularly, stay on top of her caregiver, am working to get her Medicaid, helping to manage her finances. All this I do with my brother R. and sister-in-law M. and I try to focus not only on the fact that I am doing for this for them, but that being in this situation has brought me close to them in ways that previously did not exist. So mom, thank you .

Overriding all is rage. “Radical Compassion” by Tara Brach has been suggested reading for me. Once in a while I’ll actually purchase something suggested, most of the time I’ll read a couple pages before it finds its place, in alphabetical order, on the “Definitely Later” Shelf. The fact that I’ve purchased a title in book form instead of as a virtual download doesn’t give it much chance of being read. I read mostly fiction on my iPad as it is easier on my aging eyes and for the last two years it’s been difficult to get me to read anything beyond historical fiction dedicated to The Tudors and the centuries prior to their reign.

But I have begun to read “Radical Compassion,” which discusses meditation by the RAIN method. If you’re as disenchanted with meditation as I am, I’d suggest you give this book a shot. RAIN stands for Recognize – Allow – Investigate – Nurture. Since I’ve only read about 50 pages of the book, if you like what I say go ahead and get it for yourself to see what the whole thing is about because I sure don’t know. I plan on reading more, but I’ve begun to work with the first few steps which are much more interesting – as well as more painful – than my usual way of meditation which involves sitting quietly and focusing on my breath. Then when I notice I’m thinking, I label my thoughts, “thinking,” and bring my attention back to my breath, and so on. I admit to never having given that enough of a chance – I’ve done it for weeks at a time, then lost interest.

As for RAIN, I’ve gone through the first few steps, using my mom’s Alzheimer’s as a starting point. Recognizing, which means simply recognizing what I’m feeling. Allowing, letting my feelings be. No judging, ignoring, wishing them away. Investigate – this is the interesting part. Brach writes specific questions regarding this stage in case you’re having trouble. I left out the Nurture part for now. But I came up with a couple realizations and lots of self-centeredness.

It’s not just that I’m enraged that my mom has Alzheimer’s and that I am powerless over this. It’s realizing what’s expected of me and I want none of it. I am trapped in this. My mom needs help and Alzheimer’s does not get better. It’s progressive and unpredictable. It can take months or years to reach full progression. It is costly and having taken a look at her finances, she doesn’t have what she needs which is yet more angst as I find myself wanting to screech My dad did not deal with this and I certainly am not going to! She needs daily attention and we do not know when this will turn into hourly attention. To that end, my brother and I are working with a Senior Advisor to get additional insurance in place for her to be able to get her the help she needs. The goal is to keep her in her house. Which, I might add, does not have a bathroom on the main floor nor space to add one. She can get up and down the stairs for now, but for how long?

R and M have been going the extra mile. They live closer and will pick her up to take her places. My brother works in Brooklyn and will at times stop by after work to see how she’s doing. I’m in New Jersey. Not so far, but travel there is through the Highways of Hell (for any who gets it: Garden State, Route 280, NJ Turnpike, Staten Island Expressway, plus two bridges thrown in) and the early morning 50 minute drive invariably turns into at least 2-1/2 hours to get home.

Sitting quietly and “investigating” brought up only the tip of what I’m experiencing. I’ve already known I want no part of this, that when I sit and think about it, I feel the anxiety. I am ashamed that these feelings will be seen by my brother and M and they will hate me for it. I am afraid this is going to go on for a long time and I will not be able to keep this pretense up. I am angry about what’s to come – the act of going to her house and dealing the decades-old accumulation of boxes and paper and what looks to me like junk that’s held on to for the sake of holding on. It is hard to breathe in that house, the house I grew up in since third grade, the house I flew out of at 22 as soon as I was able. Still I feel whatever I am saying here is at surface level. Still I must do a deeper dive if I’m to come to a real understanding of what’s driving me. But the closest I’ve come to something new is the fact that I have depended upon my mother to be the one to the blame and without her, without that, who am I?

© 2022 Denise Smyth

Prelude

I am angry, I wrote in my last. Once I had someone sigh and say, “That again?” Yes, that again. Like what, it has a term period? A date of ending, when I can check it off the calendar as done and over?

Truth is, what I have needed to do is slow down and pull apart the tentacles of my anger, to look at what it is these tentacles are clinging to. I’ve pushed aside, for later, what seems too unwieldy in order to peer more closely at those things I feel ready to contemplate. And there is nothing I am angry at that is not born from a lack of control. Nothing.

I am angry at the weather, the heat and lack of rain. I am angry that Trump is. I am angry that I – literally – do not know what to do when it’s my choice. Work and obligations aside, most of what I want to do is read, with maybe some TV on the weekends. That doesn’t much hold my interest, either, although I’m pretty happy with Succession. I don’t want to go out and meet people, there’s nowhere in particular I want to go, and I’m frustrated and angry that I am not someone who can say, “Hey, I’d like to ____ and then go find someone to do this mysterious activity with me.

I could go on. But I’m going to get to the one thing that angers me the most – my mom has Alzheimer’s and where to start with that? I will thank you all for your sympathy in advance. Direct it at her. While my part in this story can’t be unique, I don’t think it follows the usual trajectory in terms of feelings. But what do I know? Maybe posting this will show me different.

No matter what we’re suffering, our personalities, experiences, and habitual ways of dealing with things will surface and color our reactions, if not our actual actions. Sometimes we have the forethought to understand we might feel like saying, “fuck this” and then walking away, but something more rational takes over, sees the implications of such action, and maybe tries to do better.

Like me.

I don’t think I’ve ever really sat here and took a good, deep look at the relationship I have with my mother, who I see her as and who I see myself as in this context. In fact, a few years ago I decided I wanted to turn my blog into a memoir. During the writing it hit me how much a part of my story my mother is. There was an incident that occurred a few days after Philip died that I wanted to write and I went dumb. There I was, writing the most excruciating account, day by day, of what I felt like losing Philip, but I could not figure out how to describe an incident that concerned my mother. It was after that that I gave up the memoir, started writing much less in my blog. That is not the whole and complete reason for my withdrawal from writing. It is, perhaps, a tentacle.

Mom and I are oil and water, which I can pretty much say about my whole family. Yes, I am that one. I’d always felt on the outside but refused to think too deeply about why. I come from a large Italian family where every Sunday was spent at Grandma’s. My mom was the only girl out of seven siblings, which placed a unique burden on her when time came to helping with chores or taking care of the little ones. Two of her brothers were younger than she and she was often responsible for them. My mom’s 90, and there is one of them she still feels responsible for. In fact, in younger days when my dad was alive, the family joke was that if my dad was lying in the road and Uncle M was across the street, my mom would walk over my dad to get to my Uncle. Wasn’t any funnier then than it is now.

I used to think that maybe I felt odd because I was the only daughter of the only daughter. When Sunday dinners came around, My family would have to get to my grandparents’ extra early because my mom had to help my grandma get dinner ready. Soon as I was able, I had to do my part, whether it was putting glasses on the table or running downstairs to the club – where the men would gather and play cards while the women cooked – to get the men to come upstairs for dinner. 

Another reason I may have felt odd was because I wanted to drink. When I was 7 or 8 I asked my mom if I could have one of the cordials in that glass that just so cute. My mom said yes but my dad overheard and forbade it. I hated him then, but by 3 or so years later I figured out how to get some myself.  My grandparents made wine in the cellar, and while everyone (except the kids) drank, it was obvious that my grandfather was alcoholic. 25 Years in this county and he did not speak one word of English – only his native Italian. Many a time he’d be escorted into bed or another room, happily singing drunken tunes. Once, during dinner, there was a commotion during desert as my grandmother began hitting my grandfather over the head. Turns out he’d poured wine into his coffee cup and was blowing on it as if it was coffee because my grandmother had given him stern orders not to have wine at the table.

My grandmother lived in a two story house in Brooklyn on the top floor. The bottom, as I mentioned, was the club where my dad, my uncles and their friends hung out. On the second floor lived my Aunt J., Uncle G., Cousin R. and Cousin Maria, who is exactly two years older than I am and the sister of my heart.

I have lived very much outside the lives of the family I grew up with. Most of my uncles stayed in Brooklyn, cousins scattered to NJ, Long Island, Staten Island. My brother and sister-in-law moved to Staten Island, and I wound up in NJ with my immediate family when Philip was 7 and Natalie 5. I kept in touch with my cousin Maria on and off throughout the years – and if you’re a follower you might remember Maria was the first person I called when I found out Philip died. For the last two years I’ve worked for her and her husband, and they have graciously allowed me to escape to their shore home when I need to.

This has been a short but necessary background – next, Alzheimer’s

© 2022 Denise Smyth

Time

They must’ve told you – someone, somewhere, many someones in multiple some-wheres, how, “Time heals all wounds.” And you probably had to find out for yourself that it doesn’t. I wrote about this once, somewhere in this blog. The priest at Philip’s wake told us so and I was grateful. There is no comfort, particularly at the nadir of one’s grief, to think, in time this will go away or one day I won’t feel so bad, I will be able to manage this. When Philip died I existed in a dimension called Grief and the idea that time would heal it meant…what? That it would be okay, that I would be okay? That there was somehow going to be something called Life as Usual?

The naiveté. The shallowness. Even if said from a loving heart with all the kindness, concern and worry that comes from the helpless onlooker who truly cares for you. This month it is ten and a half years since Philip died. Since my son died. I had a therapist ask me why I called him “my son.” He is, after all, his own person, not my possession. He has a life apart from me. Except he no longer has a life – at least on this earth – apart from me. I have two children. And calling them “my child” is an acknowledgment of the bond that can be between me and them and no other. I need that. I need to know that what was and is between us is special, real, everlasting. If calling Philip “my son” soothes me that way I’ll skip the analysis of where he ends and I begin because I dare anyone with a dead child to try to figure that one out.

Then there was Phil, seeing my grief-hysteria weeks after Philip died. “Denise,” he said, “You gotta stop. Philip wouldn’t want this – he wants you to be happy.”

I turned on him. “How do you know?” I demanded. “How do you know what he wants? Maybe he’s missing me. Maybe he’s lonely. Maybe he wishes I could go keep him company!”

Phil blinked slowly. “You are really sick,” he said softly. Which fits in pretty much with the way I view myself. If thoughts wear grooves in our brains based on usage, then, “There is something wrong with me” is my Grand Canyon.

But how did he know what Philip “wanted?” We know nothing about the dead. But when it suits us we make proclamations?

I did, though, have an experience to counter this. Driving one night, not long after this exchange, I was thinking that I was going to kill myself. I once tried – and obviously failed – when I was 21. This, too, is for another post, but throughout my life I thought the only way out of the prison of my brain and the repetitive negative thinking was death. So it was natural for me to be thinking in the face of Philip’s death, “I’m done. I don’t know how yet, but I am done.”

That’s when I heard Philip. He’s behind my right shoulder, he speaks into my right ear. “Mom,” he said, “It doesn’t work that way. You have to find the joy.” And in that instant, it occurred to me that I took the responsibility of having two children, one who died, but one who was very much alive and needed me. And I saw myself standing next to Philip looking toward Natalie, but now unable to reach her. The grief was just as intense. That’s when I knew things were as they were and I must deal with them in that way. Natalie needed me. That was all there was to know.

I also understood at that moment that suicide was not a solution. It was a continuation of what I was trying to escape. If I believed death was like going to sleep and never waking up, then suicide made sense. Philip was teaching me something different. He was telling me the way out is to find the joy. I can tell you that ten years on, I have not found the joy. I still circle back to “There is something wrong with me.” I watch people, I watch the things they do and what they enjoy and what keeps them going and I still feel the odd one. My greatest pleasure is reading, which I do for hours on end daily. Today I started to write – something I have not been able to do for years even though it is one of the things I have loved to do and it was certainly what kept me going during the earlier years when Philip died. 

I have been, I am, so angry.

But back to where I started this post. Time does have a part to play. Its passage changes things. I no longer cry for hours on end every day. The constant knot in my stomach is gone. Philip is not on my mind 24/7. I can laugh. I can hold a job. I can eat. No more drinking, no more bulimia. Outwardly, no one would be able to tell I suffered such a tragic loss, that my world is upended, that I will never be the same in ways I can only accept. And that maybe I shouldn’t accept, but I do.

I have a picture of Philip from when he was maybe 5 or 6. If I can figure out how to post it under photos I’ll put it there. He’s wearing an orange pullover with a collar. His right arm is leaning on a table, bent at the elbow, his face is leaning into his hand. He’s not looking at the camera but a bit to the right, a smile on his closed mouth, his far away thoughts giving him secret pleasure. If I look, I can just make out his left hand resting on the table, clutching a small dinosaur. He is angelic. Months ago I made that picture the background on my phone and it still unsettles me to see the beauty of that innocence. It still brings me to tears, still makes me stop what I’m doing and give pause. And I would like to say I smile to see my little boy so happy and so at peace, but mostly my heart twists into something unnatural because of what I have lost and my inability to find adequate words to share this with so that maybe someone can…help? Understand? What do I want? There isn’t any help, and from those who can understand – unfortunately, there are far too many who do – I cannot take comfort. 

© 2022 Denise Smyth