
Do you want to live forever?



We named a Spotify playlist “Butterfly.” We did so because one of our last meetings before I fell ill was at the Peggy Notebaert Nature Museum in Chicago. There we watched the butterflies as they fluttered about. The children giggled as they landed on their heads and arms. We all became child-like in that place – even the adults tittered and held out their index fingers, eager for one to take respite there. It was pure glee, but I can’t help but wonder if the butterflies knew what was in store, what epic migration, one of the most significant natural events, awaited them come fall.
One of the first songs I put on the playlist was Raign’s rendition of “Knocking on Heaven’s Door,” mind you, not “Knockin’ on Heaven’s Door,” as the original version by the great Bob Dylan goes. In my mind, I cannot separate that song and the butterflies; their graceful movement, which I had seen just a few weeks before returning home for treatment, is synonymous with this track. Even now, when sitting with my coffee and gazing at our butterfly bush in our backyard garden, I watch them and mentally hear that synthy-laden, electronic drum version. Her potent, albeit angelic voice is layered and drenched in thick reverb. I initially heard it, as mentioned, just weeks after my return to commence my very 1st round of chemo (2016). So, there is an extra layer of chemo-drug-induced and emotionally consumed intensity.
The mind is extraordinary. I woke up today (August 5th) and wished my sisters a happy “Cinco de Mayo.” I was jarred awake by a landscaping crew, and in my mind, the rhythm of their compactor sounded like an MRI machine. In this hazy mental place, it wasn’t August 5th, 2021; it was May 5th, 2017, the date I was supposed to enter Mass General to begin 1 of 2 my stem cell transplant. (This was the original date, but that was pushed back by a month because of my brain surgery.) In texting them with good wishes for Cinco de Mayo, I wanted them to feel a sense of normalcy that I didn’t have on this particular date. (It is my nature to try to protect and cacoon people, especially regarding my health saga.)
It took a strong cup of coffee to pull me into the now. First, I began thinking about my strange wake-up and where I was in mind and heart. Then, as it has been a while since I have listened to it, I put on Raign and sipped more coffee.
Little did I know then that the Peggy Notebaert Nature Museum was this sacred little bubble. Not only for me, though for obvious reasons it was, but it seemed that way for everyone there. The laughing children, the adults who regressed to a child-like place, all stepped away from the world. Then, as my mind does, at least when it’s fully awake and has a bit of coffee, I thought about the people in that blissful bubble and the butterflies fluttering about. Who was giving whom a respite from life; was it the humans gazing in awe at these gorgeous little beings, taken away from their worries and stresses, even if just for a minute. Or was it the butterflies developing a divine connection with a human by landing on their index finger or soaking in the gleeful laughter of children before embarking on a migration of epic proportions?
I will undoubtedly wake up again in a place and time far from here within the next few days. This isn’t solely for the benefit of others, to grace them with a feeling of normalcy, but also for me. I have routine bloodwork in a week (August 11th) and an oncologist appointment two days after.
Maybe I will wake up thinking I’m a butterfly.
“Once upon a time, I dreamt I was a butterfly, fluttering hither and thither, to all intents and purposes a butterfly. I was conscious only of my happiness as a butterfly, unaware I was myself. Soon, I awaked, and there I was, veritably myself again. Now I do not know whether I was then a man dreaming I was a butterfly or whether I am now a butterfly, dreaming I am a man.”
Chuang Tzu (c. 369 BC – c. 286 BC)

I fancy myself a bit of a writer, a wordsmith. I never had the confidence I do now to write. I was always worried about my grammar and punctuation. More than anything, I was worried about opening up and spilling it all out, letting the floodgates open and setting for a deluge of emotions, feelings, and thoughts that would potentially leave me exposed to criticism or judgment. After diagnosis, I stopped caring. The last thing I would concern myself with was grammar. Next in line, or perhaps going hand in hand with grammar, were the thoughts of others. I was already emotionally raw on so many other levels; I might as well leave it all wide open.
Today I met with my oncologist, and, as I expected, it was decided to “keep an eye” on things. The recent MRI showed hemosiderin deposition in the brain, which isn’t as bad as it sounds. These deposits transpire after bleeding has happened, which can occur after any traumatic injury to the brain. The bleeding leaves behind stains and, in time, is broken down by the body and left behind as iron deposits. This is my basic understanding. There is some question as to whether or not this could be residual neoplasm, leftover cancer cells. This raised the question in my mind as to whether or not this is why my tumor markers are rising ever so slightly. But, as stated, we’re just going to keep an eye on it.
keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it. keep an eye on it.
This is when the longing to be a wordsmith falls away.
The old and young. Young and old. What a madhouse here. No rhyme or reason at the cancer clinic. I sometimes want to ask, in a clandestine whisper, ‘Hey you, ya you! whatcha in for?’ ’cause that’s what it’s like. I’ve never been in jail, but I can imagine what it is. I’ve been in a different kind of prison for four years, or has it been longer? I can’t remember. That’s the problem with these days that blend into months and then merge into years; they all look and feel the same. It’s worse in treatment. It’s always worse in treatment. Even today, a beautiful day, and I swear it was May, yet I wrote March 24 on my intake paperwork. “So, doc, ain’t I done good?” I ask as he studies my file and randomly looks up at me. “I’ve been good, I swear! I’m free to go, right?” I want something. I am seeking something; everyone is seeking something in treatment or after treatment. Craving the words, “You’re good!” Oh yes, they call us survivors; what a strange name. I’ll know what this something is, what it’ll be once I get my claws sunk into it. “Well, why don’t we keep an eye on it.”
I schedule a follow-up, bloodwork and scans for a later date. But it wasn’t me. I planned them for my body to be aware of my physical being and its course. But emotionally and psychologically, cancer is no longer.
To be clear, emotionally and psychologically, cancer no longer has me.
Follow-up scheduled: COMPLY (Y/N) Y
Current objective: to be and enjoy being? COMPLY (Y/N) Y
Worrying Overridden: COMPLY (Y/N) Y
Outer Stability Seeking: COMPLY (Y/N) N
Inner Stability Seeking: COMPLY (Y/N) Y
(Physical) Cancer Status: Tracking/Monitoring
(Emotional/psychological) Cancer Status: NED (No Evidence of Disease)
My first brain MRI was in Chicago after being rushed to the ER. I woke from a seizure stuck inside a device that hummed and rattled with a disembodied voice telling me not to move. As I recall, it wasn’t a pleasant voice. However, in defense of the tech overseeing the procedure, I struggled to free myself. In my defense, however, who the fuck wouldn’t? I was reentering the world from a seizure; I didn’t know who I was or where or, for that matter, what I was. I was there, semi-conscious, with my head stuck inside an unknown object that seemed to be pulsating. “Jeremiah, don’t move! If you do, we’ll have to start the procedure again!” So, I stopped moving; instead, I just cried.

What I remember, even more than the terrifying sounds, the somewhat annoyed tech, and the tears, was my thirst. My god, the craving for water was so intense. My tongue was leather-like in my mouth. When thirst surpasses fear, a new level of a primordial being emerges. That is the creature that remained on that MRI/scan bed, the being who rested motionless and withdrew inward. I do not know any other word to describe the sensation better, but “withdraw” is most suitable. It was as though Jeremiah split into two halves, the person being tested/scanned and the one full of desperation. In between these was where I ended up and withdrew, holing up in a chasm. I remember resting my hands by my side as if I were a windup toy that had just ended its cycle. I’ve always wondered what the MRI tech thought. Did they see me slip into that place, that point between two worlds, the chasm I mentioned?
The “scanxiety” is everpresent; how could it not be? However, I understand that my genuine fear is detaching. I am concerned about stopping as I did before within that gap between the two halves amidst those two worlds. The horror of a potential recurrence is no longer as intense as it was, even with the tumor markers that are trending upwards ever-so-slightly. If it ever does return, I’ll deal with it. I dealt with it when initially diagnosed and again with the recurrence. After numerous hypnosis sessions, it is evident that my worry of withdrawing, psychologically and emotionally disengaging, far surpasses my concern of a recurrence.
As I have discovered, and most already know, cancer can be managed and treated in numerous ways. The withdrawing, the derealization I speak of, isn’t controlled or cured in such a targeted manner. I feel more detached with each MRI. Amid each procedure, the tech, be it for an MRI, CT, etc., needn’t tell me to “stop moving!” as I keep finding my way back to that middle ground, to the chasm.
I’m unsure when it started, but I have felt tenderness and a dull ache in my testicle for the last few days. Naturally, this has set off every alarm in my mind; every possible worry and concern has crept back into the light. After four years, I would have assumed that the fear of a recurrence would have lessened, but it has come raging back with this feeling.
The other night, I dreamt that I was back in the treatment chair, and the nurses were trying to fit in an IV. Each nurse attempted dozens of times to no avail. Finally, the nurse, who, in waking life, I see every time I go for labs, said, “Jeremiah, I’m sorry, but we can’t fit the IV. We’ll try again tomorrow.” Then, I shifted dreams, but I am unsure what followed.
In my unconscious mind, these worries are ever-present; they have always been. It isn’t just with this feeling and sensation. My dreams regularly reveal so much; every emotional state, good or bad, is magnified tenfold within my dreamscapes.
I dream journal. I try to do so every day. I have stopped writing out the dreams in a descriptive manner. I don’t set out to write short stories-like entries when I awake with one still fresh in my mind. Instead, I pull imagery from them. I snag tidbits of information, perhaps the color of an object or a particular look I receive. However, with the dreams that revolve around cancer, I am tangled up in internal sensations and feelings more than anything external. Something in the dream mentioned above, which has occurred in various iterations for years, prevents me from being treated. I want to hang on, stay within the dream, and ride it to the end. Would it make sense once I got there, wherever there is? What answers would I receive? Would it make sense – would any of this make sense?

I have dreamt dozens of times that cancer has returned. Not testicular cancer, not necessarily, just cancer in general.
The other night, I awoke, and, having fallen asleep on my arm, it was numb from the shoulder down. This, too, has happened numerous times, but I am always so shocked and horrified that I sit straight up in bed each time, flop my numb arm over my lap, and await as it comes back, as it awakes as well. I hold my breath. In the middle of the night, I sit in the dark, cradling my arm and waiting. When I feel the gentle tingling sensation return, the soft pins, and needles that signify it has awoken, I lie back, relieved. It is then, and only then, that I realize (the) cancer hasn’t returned. Another lesion hasn’t formed in my brain. I don’t need brain surgery.
Incidents such as this are not uncommon. This is but one example…
This fear lurks; I feel as though sometimes it is stalking me. Other times I know that, at this moment, I am cancer-free, it is out of my system and a thing of the past. I am torn between these two worlds of quaking fear and joyful bliss.
I recently had a conversation about this very feeling, about how I feel that I am often shadowed by cancer, that it is pursuing me. I was unaware of its presence upon initial diagnosis. When struck by the recurrence, I was completely oblivious as with the first time. So much so that when my oncologist told me it had returned, I was in denial. Naturally, anyone would be dismissed, as this is the last thing one wants to hear after being treated once. When I was informed, I felt 100%; my body felt so strong and healthy. I wouldn’t believe it – I couldn’t accept that it had returned. Regardless, it had, and both times it snuck up on me and pounced. I blinked, and it was upon me; claws sunk deep, and I was helpless.
I suppose this is just something that lingers. How long is uncertain. Perhaps it will always shadow me. I hope it will do so in such a way that it is not hunting me, or for that matter, haunting me, but a reminder of what has come to pass.
Patience! I need more patience with myself as I move along this path.

i cannot tell
which is more patient
the tree
like gnarled old fingers
sun-beached and
long since passed
or the days and nights
which move around it
we witness the blue sky
so rich and clear
and mistake our need
we forget tolerance
we say
“get out of the way
you old tree
I want to see the blue sky”
but the tree
is the gentle one
by day
it marks the earth
with the movement
of the sun
across the sky
not rushing it
letting it be
moment by moment
and at night
it stands
almost sentry-like
keeping watch
waiting
it never says
“you are gray today
bring back
your blue sky”
if it is unable
to mark the earth
as a sundial would
it just waits
gnarled and old
like it was yesterday
as it will be tomorrow
I arrived early at the Bourgeoise Pig Cafe, a small tea house in Chicago’s Lincoln Park. I was anxious, more so than usual. After the calm of coastal Maine, Chicago’s busyness was unnerving, and the news of my recurrence made every part of me tense.
I had to return! I postponed the treatment by a week so that I might see my then-girlfriend. My illness arrived when our relationship was in its infancy. As such, we clung to one another, even from afar, trying to come to terms with the storm that had just hit. But that’s a story for another time, perhaps only between her and me.
I ordered a panini and tea and then slipped off to the bathroom to gain my composure before Jose arrived. I always felt this deep connection to Jose. He was a mentor, an older brother, and a performance art partner. More than all that, he was just a dear friend whose very nature was comforting and gentle.
We met at the Bourgeoise Pig Cafe because I wasn’t ready to travel north to Edgewater. It was only a matter of several stops on the red line, but I couldn’t do it. It would mean passing by the L station where I had my initial seizure, where everything began, and my life changed. I hadn’t been there since the incident; I hadn’t even returned to Chicago.
That particular L stop has returned to me in different forms of daydreams or mental images. It came to me today, which is why I wrote this post.
I am not sure how it appeared or what stirred the memory. I suddenly found myself between my apartment and Thorndale, the station just a few stops from the redline’s northern terminus. I stop and take it all in when I find myself in these places of reflection. In my opinion, letting the mind drift away in these moments of reverie is healthy and natural. I think we have misunderstood this notion of mindfulness. With all our apps and smartphone reminders telling us to “be here now!” we are struggling and even feel guilty for letting ourselves drift and be open to allowing our minds to enjoy their natural ability. Being fully conscious of where one’s thoughts are and where they are going is very powerful. I became very aware of this while inpatient during my back-to-back stem cell transplants. My confinement within a sterile room for weeks and being all but bedridden would have proven far too significant an obstacle. Consequently, I allowed my mind to go — consciously permitting it to be like a balloon, one tethered to my hand but floating above, being pushed about by air currents, etc.
Today, those currents took me back to Chicago, and I found myself between my apartment and the Thorndale L stop.
I admit I feel lucky When I look back at one particular event from that day. I know how strange it is to say such a thing, and perhaps it isn’t even the right word in this context. Though, to say I feel blessed conjures up far too much. I am thankful for my childhood and having been raised catholic. Having a spiritual-based upbringing allowed me to explore religions as a whole – global religions, all of humankind’s beliefs. However, blessed, even with etymological roots that far transcend those I associate it with, still conjures up notions that are so intrinsically linked to my upbringing that I can’t put them aside.
My mind brings me back, and I return to that day. I watch myself. I see myself on the street full of children on their way to school and commuters heading to the L stop. I feel the late March sun on my face. I hear the traffic that stops and proceeds and stops and starts again as the lights rhythmically change. Where am I? I am across the street, waiting for the light to change so I can cross the road, but in no real rush as the sun is far too gorgeous to be concerned about much of anything. No, I am watching myself inside the cafe on the corner of Thorndale and Broadway. I enjoy mug after mug of comforting dinner coffee served in thick-walled cups. Wait, I am a boy passing by, laughing with his friends as they rush off to school. We have postponed going, bewitched by the March sun; we have lost all fear of the repercussions we might pay for being late. I am in the car, stopped at the red light. I’m sitting, engine idling, whistling slightly off-pitch to a pop song on the radio I’ve never heard before. No, I am the businessman, elegantly dressed, coffee in one hand, briefcase in the other, ready for the day.
I am watching myself. I have returned here a dozen times and taken on numerous roles. Each one is fully aware of what is happening or, instead, what will happen. Standing across the street, preparing to cross, the man has forsaken the glorious sun to watch me instead. The man in the cafe stands up to observe. Usually, he stops for nothing, especially on his morning commute; the businessman halts midstride. The boy, who has forsaken the bell and the consequences of his tardiness, stands still. The man in the car doesn’t care about the line of cars behind him; he follows my every step.
It’s horrible to watch; it sickens us and turns our stomachs. It never gets easier. We are witnessing ourselves in a place of such fear. We know now what is happening. It has happened so many times since. Then, however, it is the first time, and each embodiment feels it. We cringe as our body stiffens into such an unnatural and horrific form. As our physical self contorts and breaks and releases some ungodly howl. And when we fall, when our body cannot hold itself, we recoil at the sight as our beings’ weight hits the ground so hard we bruise our very bones. But even as each one of us wants to look away or even wretch at the site, we say, “Thank you.” It isn’t for the years of pain that will follow, of absolutely not! We now understand what could have been – what very well could have been – if we made it to the station, up the stairs, and to the platform.
The Thorndale red line stop is narrow; a few adults could link arms and span its width.
On that horrific day, I was roughly a hundred steps from this station: a hundred paces and a short flight of stairs stood between me and the platform. I can’t help but wonder. I cannot help it! Perhaps it was the crosswalk that impeded my journey? Did I have to wait that long for it? Maybe a rambunctious school child, delirious from the fresh air, bumped into me and slowed me down? Or that businessman, walking with beeline precision, forced me to sidestep. Or… or what?
But I didn’t make it to the station; I didn’t make it up the stairs or the platform. Had I, what then? Had I had a seizure on the platform, would the tracks have swallowed me up? Would I have fallen inwards towards the center of the narrow platform, towards safety? Or outward… outward and downwards; downwards into the train’s path or onto the tracks housing 600v of electricity?
But I didn’t; I didn’t make it to the station, up the stairs, or to the platform.
During the same trip, I did manage to go up to Edgewater. I prepared myself for the stop at Thorndale. I was white-knuckling the seat, only realizing how intense I must have looked when I met another passenger’s gaze. However, the L will often run trains express, bypassing several stations. The train I was riding ran express from Berwyn to Granville, one stop farther north than Thorndale, thus avoiding it altogether.
I took a Lyft back to Lincoln Park. I wasn’t ready. I intended to take the red line south but exited the Granville station.
Maybe I’ll never be prepared to return to this particular stop. Or, if I do, Jose and I will grab paninis and tea at the cafe and enjoy them on the platform. Maybe we’ll sit in silence. Or perhaps we’ll talk about the things we each feel blessed for.
Our situations were identical in almost every way.
He was diagnosed with testicular cancer. His staging was the same as mine. He, too, experienced a recurrence that presented as a brain lesion and opted for a stem cell transplant.
This is where our paths split apart. Shortly after his high-dose chemo treatment commenced, prepping his body for the transplant, he became increasingly confused and disoriented. After sets of scans were performed, it became evident that, though the heavy rounds of treatment were well underway, several more lesions had presented themselves in his brain. The decision was made to stop treatment and return home, enter hospice care, and be around loved ones. Shortly after he decision was made, he passed away.
Even in writing this, I don’t know where to begin opening up my emotional state regarding his journey and mine and where they veered off and split from one another. I shudder thinking about the fact that my lesions could have multiplied, too. Or, for that matter, the one that did present itself could have been in such an area that it was deemed inoperable, leaving me with more complications than just a stroke and a paralyzed arm. (“Just a stroke…”) What damage could my tumor have caused had it been slightly to the left, to the right, etc? Was I naive to postpone my 2nd round of salvage chemo and head out to visit Dr. Einhorn in Indianapolis to get a second opinion? Was this delay dangerous in such a way that… it’s too much to think about.
These questions haunt me. They wake me in the middle of the night. Even more so is one I can’t escape asking repeatedly: why am I here and he isn’t? Why am I alive and he … and he isn’t?
I never understood survivors’ guilt. I had heard about it but never truly understood it. Yes, on a larger scale, anyone who survives cancer thinks about all those who haven’t and, in one way or another, has that feeling. In most cases, guilt might be too harsh, but this particular scenario is apt.
I loop my posts back around. With my last sentences or so, I always seek to return to the overall idea. Is this good writing? I’m not sure. I do so to keep everyone along the way. My writing tends to drift a little far out, so bringing things full circle will hopefully lead people to say, “Oh, now I understand why he wrote…” However, with this post and the subject matter herein, I can’t. How do I bring this back around? What closing line or thought can I inject here? Nothing can sum this up or deliver on one’s need for coherency as none of this makes sense…
Perhaps this is survivor’s guilt. Maybe it isn’t so much about feeling remorse for those who have passed at the hand of this insidious disease, but rather the inability to make sense of it, to articulate it to ourselves and others. As with this post, I want to bring it back around so it feels wholly desperate and there is some understanding to accept the madness of this life and the injustices that rear their heads. But I can’t. Everything is left hanging, nothing but loose ends, dangling strands that I keep tugging at…
Be well on your journey, Alex
June 13, 1994 ~ June 30, 2020 (age 26)

This summer will mark the 3rd anniversary of my stem cell transplant! It is hard to believe that so much time has passed since that long and very trying span of time, from June to August of 2017. So much has come to pass; so much growth on a personal level, so much understanding and acceptance, so much physical and emotional healing.
Even if I look back to just half a year ago I am left scratching my head asking, ‘who was that?’ I suppose this is normal, but I am hyper-vigilant of the passage of time, as I’m sure every cancer survivor is. It isn’t so much that I’m counting every second and rejoicing at every tiny gulp of fresh air I am graced with. No, it isn’t like that. Naturally, I am very lucky. However, I feel graced with, if that’s still the most suitable term I want to use here, with the awareness and shifts within myself. Call it “soul” or “spirit”… whatever word you’d like, I won’t label it so as not to taint one’s vision of how I’m perceiving this “inner” part.
Several months ago, I was experiencing a nervous breakdown and was admitted to a hospital in France. Really, who was that? I needed that, of course. I needed to bottom out. My body was already working on slowly repairing itself, but I hadn’t yet allowed myself to crash on an emotional and psychological level. My inability to hold on slipped and I did… I crashed hard – very hard. As difficult as it might have been, this was when the shifts began to occur.
3 years ago, I was watching fireworks from Massachusetts General Hospital’s cancer ward. I tried to sweet-talk one of the nurses into getting me a beer so I could, like a lot of my fellow Americans, sit and sip a beer while watching the display, all the while exclaiming, “Ohh!” and “Wow!” She said no and gave me another anti-nausea med and an ice cream. The fireworks didn’t live up to their hype. I heard good things; a lovely display of colorful explosions seen from the 10th floor of a building overlooking the Charles River. It sounded amazing. Though various buildings obstructed our view, we couldn’t see The Charles. There were perhaps ½ a dozen patients and nurses. It was an interesting and also eerie sight, all of us in masks and gowns; the patients seemed quiet, in that middle ground of toxicity-induced psychedelia and being fully present. I shouldn’t generalize, but I often found myself in this state, always ready for what I am unsure. All of us were tethered to our IV poles, which pumped an alarming amount of chemo agents into each of our bodies or flooded us with other various fluids. The nurses talked amongst themselves, texting and doing things normal people do. I don’t remember the grand finale. The other patients and I left the room with the promised vista of fireworks overlooking the Charles, wheeling their IV poles alongside us. I heard the muffled explosions from my sealed-off room, just a gentle murmur that was barely audible underneath the continuous hum of the air filtration system.
Every 4th of July I remember this. I remember that room on the 10th floor of Mass General’s cancer ward and the patients wheeling about IV poles, hoping to see a clear view of fireworks but, in the end, not really caring. Or maybe I cared in that way cancer patients care about things that, though they would be nice, weren’t of the highest priority at the moment. Or perhaps, like me, we all wanted to enjoy the goddamn fireworks while drinking some shitty beers and be normal, feel normal… whatever that was at the time. But alas, we all returned to our rooms to resume our treatment or our sleepless nights of nausea and delirium, or the darkness-induced existential terrors, fears, and tears, to everything (everything!) else that takes precedence over fireworks.
I don’t look back on it now, every summer, every 4th of July, and feel a sort of unease or anger, etc. I feel this reaction with other things, naturally. Other dates are inescapable; those, too, have lost their bite. The day after Mother’s Day 2017, I had a stroke, which paralyzed my left arm, postponed my transplant, and sent me to the hospital for brain surgery. I watched the solstice sun (image attached) lazily creep across the sky from my room at Mass General.
These are there and solidified in my personal journey and my personal history. They’re not so much pitfalls anymore in the yearly cycle, so much as pitstops that allow me to recess my place within all this and the growth within myself.

Today is National Cancer Survivor Day.
I have been compiling some comparison photos. The ones of me during treatment, which were taken during my inpatient stay at Mass General, were so hard to look at for the longest time. It is still unnerving. When I upload and then delete photos from my phone these photos, as well as a few of my family, are the ones that always remain.
In the last several months, I have only been able to pause, look at them, and consider who that person was and what aspects of him still remain. The shift in this ability, that of being able to witness this previous Jeremiah, came after my psychological and emotional hardship experienced while abroad in the fall ‘19. Since then, things have started to dissolve, things that have been carried and dragged too far for too long. Perhaps this is why I can look at this photo with more compassion and kindness. Yes, there is still fear, of course there will always be fear.
During these years of survivorship, some people have drifted out of my life, as any path to any destination worth arriving at isn’t free of bramble and vexation. Others have grown increasingly closer to me, and in sticking with the path analogy, our comradery has strengthened, allowing us to work together through the dense underbrush that is life.