Paul's Heart

Life As A Dad, And A Survivor

Archive for the category “The Heart”

Surviving Guilt


We know when we have done something wrong.  We also know if what we did that was wrong, was intentional or by accident.  Sometimes, something wrong may happen and we have no idea why.  But whether we recognize what we did, or whether it has been pointed out to us, under normal circumstances, we know what happened was wrong.  We feel bad.  Our conscience reminds us that we did something wrong.  And then hopefully, we can correct what has happened, apologize, and move on.

There are jokes and memes all around about different types of guilt from “Jewish mother” guilt, Catholic guilt.  There are more serious forms of guilt, such as those who commit crimes or other harm to people.  Guilt can be either healthy or unhealthy, depending on how you let it impact your life, especially if you cannot, or will not let it go.

This was a picture that I never thought I would see.  Estranged from my father, both of us having our reasons, one tragic night reunited us together, in a direction of healing.

My father carried a lot of guilt with him through his years.  I was just one source.  Obviously, there was my childhood, which he missed most of.  And then there was his absence during my battle with Hodgkin’s Lymphoma.

But an accident on a cold Winter’s night in December, just days before Christmas, left my father’s “cup” of guilt, overflowing.  He could handle no more, and sadly, more was going to come.

My father and stepmother had gotten into a heated argument.  Being just before the holiday, there was still some last minute shopping to do.  Having to put the argument aside, my father left the house to start the car and warm it up.  As my stepmother followed shortly after him, crossing the poorly dusk covered street, my father watched in horror as she was hit by a car, who had not had their headlights on yet.

Though my father’s attentions clearly were focused on the immediate medical needs of my stepmother, clearly my father could not stop thinking about what happened earlier that night.  He felt that had they not had that argument, at the least, he would have been crossing the street with her, and perhaps he could have seen the car, or at least taken the brunt of the impact.  He felt responsible for that evening.  He felt… guilt.  And because he could bare no more, he needed to release at least what he could.  The damage that my stepmother suffered, was permanent, and that guilt he would never be able to release.

The apple has not fallen far from the tree.  Like my father, I would accumulate guilt, some that I have been able to release, and some, like my father, I will likely carry to my grave.  And to the average person, this makes no sense.  “Just get over it.  It is no big deal.  It has nothing to do with today and now.”  If only it were that easy.

One of my first memories of something I remember doing wrong (not me in the picture), was throwing a snowball through a window.  Sure, not the smartest idea, but it was a light snow, not slushy and hard, definitely did not expect it to do damage, but it did.  And my friend got blamed for it I would later find out.  As soon as I found out, I admitted my fault.  There are a few of these stupid moments in my life as a child.  In these cases, while the actions were bad, the guilt was actually healthy, because it taught me accountability.

Then there is the unhealthy guilt.

My grandmother was my world, my moral compass.  She was my first immediate contact with the world of cancer having been diagnosed with breast cancer in 1986.  In 1998, she was diagnosed with her second cancer, ovarian.  As she was about to begin her chemotherapy, I stopped by the Saturday before just to visit her, as I often did.

Keep in mind, I had already faced my Hodgkin’s Lympoma nearly ten years earlier.  As soon as I walked into her house, I could tell something was not right.  On the dining room table was all of the literature, pertaining to things that she would need to know about going through chemotherapy.  None of it had been touched.  I wanted to think my grandmother was just neat about it, but there were no “folds” in the booklets to even provide evidence of being opened.

As I sat across from her in the living room, I noticed that she had cut her hair real short, buzz cut length, something I had never seen before.  Clearly a sign that she was preparing for what lay ahead side effect from her chemo.  But something still did not feel right.  She was withdrawn.  Barely a word was said during the hour visit.  Her thoughts were clearly elsewhere.

As I prepared to leave, I told her that I would visit her the next day.  Of course I was hoping she might seem a bit more “up” in spite of what she was facing.  I cannot explain what happened next or why.  Typically, when I left my grandmother’s house, I gave her a hug and kiss goodbye, and told her I loved her.  This Saturday, I did not.

That next morning, I was at church, when my grandmother called me.  She informed me that she was going to the hospital, that she was not feeling well.  When I told her I would leave right away, she told me to stay where I was.  I ran a youth group, and she knew I had an activity later that morning into the afternoon.  She told me that she would see me later that evening as originally planned.

Later that afternoon, during my youth event, another phone call had come to the church.  This time, and I honestly do not remember who it was that called, but the message was, my grandmother had died.  I was devastated.  Not just for the loss, but the fact that the last time that I saw her, was the only time, I did not tell her that I loved her.  I would never get that chance again.

Like my father, a guilt that I can never release.

As a rule, from that day, I have dealt with any issues, right at that moment, or as soon as possible.  The expression, “do not go to bed angry”, an important lesson both my father and I learned the hard way.  You may never have the chance to make amends.  Fortunately, there are not many things that I have done that have left me with any burdens of remorse.  And for the most part, if there are any, they involve my daughters and any absences that I may have as they have grown, a result of a divorce.

Especially this year, Covid has wreaked the most havoc in being able to spend time with my daughters, especially during the early weeks of the pandemic.  With no plans or structure in place how to deal with the outbreak, and me having a compromised immune system from my Hodgkin’s days, the most difficult of decisions had to be made, to cancel visits.  We live a distance apart, and safe travel arrangements needed to be arranged, and at that point, no one knew what to do.

But unlike my younger days, and like that of my father, I deal with my actions right away, giving the opportunity to heal and move on.  My daughters understand my health issues and struggles.  It does not make the losses any less painful, but it matters that they understand.

The toughest guilt of all to get through, not just for me, but for so many others, is survivor guilt.  Typically associated with those who have survived wars, natural disasters, tragedies and other accidents, survivors of cancer often develop guilt.  And the response from the “non-cancer” world is always the same… “you have nothing to feel guilty for, surviving cancer” or “how can you feel bad for surviving cancer?”

It is not that simple.  For instance, in my case, while Hodgkin’s Lymphoma has a fairly high cure rate, its treatments have cost me greatly with my health and late developing side effects from the chemotherapy and radiation therapy.  But again, here come the chants, “but you are still here!”  Again, it is not that simple.

These are just some of the wonderful people I have gotten to meet over my survivorship of over thirty years.  But they are all gone.  Some from the cancer, some from immediate side effects, some from late side effect issues.  They all had Hodgkin’s Lymphoma like me.  And there are literally hundreds of more photos I could post.  Why them?  Why not me?  What is so special about my body, that I am still here and they are not?

Yes, I know.  What I am really saying is, “it is not fair.”  Obviously cancer is not fair.  It does not matter how old, if you have family, if you are riding a huge wave of success.  The fact of the matter is, and I realize I do not possess the power to make the sun rise, or the waters to flow in the rivers.  But these friends of mine, deserve to still be here.  I am.  So should they.

That is survivor’s guilt.

I have spent almost as long in my survivorship, in therapy dealing with my survivorship guilt.  I have written articles and other special publications about the topic.  And still, here I am, literally and figuratively.  Still dealing with it.

9 Lives


I have often said that I feel like I must have been a cat in my prior life.  And if I was indeed reincarnated from a feline, that I hope it was at least from either of the two mighty big cats pictured above.  That would certainly explain the “fight” I possess in my character.

One of the most difficult conversations to have with a child, as a parent, is when that parent faces a difficult crisis, especially one that involves health.  The only thing more painful for a child to experience than the loss of a parent, is to watch one suffer.

So, the conversation in my many circles of cancer patients and survivors is, “when do you tell them, and what do you tell them?”

To be honest, it is going to be an individual decision each time.  But it should always be age appropriate.  One story I recall my father telling me, was that he was told his mother went into the hospital for gall bladder surgery, only to die from gall bladder cancer.  He had been lied to.

This would come back to haunt him later in his life, when I would be diagnosed with cancer, Hodgkin’s Lymphoma.  The images that were permanently etched in his memory, were of his mother, suffering, in pain, and dead.  Years later after my battle, my father would have a conversation that haunted him for years, explaining to me, why he could not bring himself to visit me following my diagnosis and during my treatment.  I may not have understood originally, but over my decades of survivorship, I definitely get it.

I have two daughters, both teenagers currently.  They were not even of this planet when I dealt with my cancer, but halfway into my survivorship, they have been witness to the many issues that I face, resulting from late effects caused by my radiation and chemotherapy treatments.  Fortunately, for most of these events, they were too young to really remember what had been happening.

As they will soon be adults, too soon for my comfort, they will end up being my medical proxies as well as my legal representatives should something happen to me.  And in order for that to happen, and work, they will need to learn what I have gone through, understand the seriousness, and most importantly, know what I want.

Like I titled the post, 9 Lives, during a recent visit with my daughters I began the conversation referring to nine lives, the mythical belief that cats somehow get nine swings at life.  It was a lighthearted method to introduce the serious events in my life, but in a way that showed I have a lot of fight in me, and the will I have to get through those things.

Life #1

I have not gone into great detail about my experience with Hodgkin’s Lymphoma.  But they get the seriousness and odds of fighting cancer.  If there is one thing my daughters are not shy about, it is inspiring others who may face cancer, “our dad beat cancer 30 years ago.  You can do it too.”

Life #2

My daughters were not even in school yet, when I faced my fate for the second time in my life, this time with something referred to as a “widowmaker,” a blockage of the main artery to the heart.  I was dying.

They know I had heart surgery.  But to this day, they do not know how serious it was.

Life #3

Four years after that surgery, another event would happen, also courtesy of my late effects, and another potential silent killer.  This time, I would be taken out of my house, at 4am, on an ambulance stretcher (I will go into this detail in another post, it deserved its own).  One of the few memories I have of that evening, is seeing the faces of fear and confusion on the faces of my young daughters as I was wheeled passed them.  During their last visit with me, I asked them what they remembered of that night, again, fortunately not much, except one could not wait to get back to sleep, the other surprised by all of the police officers in the house to help.

I had something called “aspiration pneumonia,” and I was septic.  In fact, blood tests would reveal I was septic for 48 hours.  Unbelievably, I was unaware that this was happening when I went to bed that evening.  Simply put, sepsis kills.  Time is important.

Life #4

I would have a repeat of the aspiration pneumonia nine months later, this time in both of my lungs.

Lives #5 and #6

Not medical, but both events that could have turned out way differently.

I had been through several hurricanes in my life.  But Irma was the first one that I actually experienced going through the eye.  Unable to evacuate for many reasons, all I could do was stay sheltered as best as I could.

The other event, a major car accident.  One thing I take pride in, is my safe driving record, no accidents in over 40 plus years.  Until one night, someone went through a red light, coming straight at me, head on.  I made a last second maneuver to avoid the head-on impact, instead to get t-boned (crashed into the side of my car).  Fortunately, I was not hurt.  The car was a total loss.

Both times could have turned out way differently.

Life #7

Just passing mid-life a few years ago, clearly I have been using up these “lives” at too quick a pace, and another issue with my heart came up that I was not expecting.  Because I am being followed by a specialist with my late effects, I was already aware that I do have other heart issues.  We are all watching them.  This one I did not expect.

A test that had not been done in nearly a decade showed that I had another major blockage.

So, back when my original “widowmaker” was corrected, I was told I would have a triple bypass.  When I came to, I was told only two were done.  The RCA artery, was not considered bad enough to bypass, unlike the LAD.  Only one problem, the damage to the LAD, was just taking longer to develop in the RCA.  So, since they did not fix the RCA when they had the chance, guess what got fixed eleven years later, along with another lecture on letting things go.  You see, doctors assumed with the blockage, I should have been experiencing symptoms.  Truth is, I know what I felt like originally, I did not have those symptoms this time.

My older daughter has developed an interesting sense of humor and has not been shy about this fact that I have apparently used up, seven of my nine lives at this point.

Yep.  I need to somehow slow this process down.  But if there is one thing my daughters have learned about me, a past life as a cat or not, my younger daughter describes me as one of the strongest people she will ever know.  I wish I felt like she describes me, there is no doubt what I have gone through has been difficult.  But I have so much more to do, that involves both of them, a deal that my doctors have all agreed to do their part to make sure I get to see those days… graduations, weddings, grandchildren.  I want to be clear, while I am looking forward to those last two things especially… there is no rush to get there.

The Toughest Part Of My Heart Surgery


A post from a fellow Hodgkin’s Lymphoma survivor triggered an emotional flashback for me recently.  A young parent themselves, one of their main concerns, is for their young children, and this will be the first time that this friend will be apart from their children for any amount of time.  Even more relatable, are two main factors, this fellow survivor is having open heart surgery, and their children are the same ages as my daughters were back in 2008.

My daughters were three and five years old, and had never been apart from me.  I went from just telling them, I had to go stay overnight somewhere for something special, but would see them the next day, to the horror 24 hours later of thinking I would never see them again.

A blockage had been discovered that was believed correctable with a simple stent being placed.  I would be up and going in just a week, an overnight stay in the hospital.  No big deal.  I was still coming out of the anesthesia that day, when the doctor was informing my family, my situation was more grave than thought, and instead I would need to have open heart surgery the next morning.  You can read the story “CABG – Not Just A Green Leafy Vegetable” for that whole situation.

But as I came out of the fog from the anesthesia, and began to understand the severity of what I was facing, there was even a more daunting concern for me.  If anything bad happened to me during this surgery, I never got to see or hold my daughters again, especially before the surgery.

I am a firm believer in not discussing things with children that are not age appropriate, and this was something that was not going to be discussed with them in great detail.  But that did not make my heartbreak any less.  Even if the surgery was successful, I would be in the hospital, expected to be about a week in length.  I had never been apart from them at all, even until the day before for the stent process.  I got to talk to them on the telephone that night before, and that was going to have to be good enough.  In less than eight hours, I would be taken down to the operating room.

Three days following the surgery, out of the ICU and in a private room, I still had some tubes and wires, but not nearly as many as when I first came out of the surgery.  At that point, it was decided to bring my daughters to visit me, a surprise visit, because they were all I could think about.  My older daughter was curious about all the equipment that I was hooked up to.  And the joke, er… concern, was that she would not do to me what she did to her mechanical horse Butterscotch, when we were not looking and she started pulling the horse’s wiring apart.  My younger daughter on the other hand, sat on the foot of my bed.  This was the first either of them had seen me in this type of condition, and clearly she was scared.

The picture above, was taken a couple days after we got home, no worse for the wear.  In fact, my younger daughter had resumed her playfulness with me, forgetting the fragile area of my chest, starting from across the room, running full tilt at me, unsuspecting, planting her head into my chest like a battering ram.  That was when that “heart” pillow came in handy besides my coughs and sneezes.

My daughters would witness another event, just as severe, and probably more scary, because they watched it happen in real time.  After just celebrating my older daughter’s birthday  that day, an ambulance crew was rolling me out of our house on a stretcher, again facing a dire situation, septic shock, due to a specific type of bacterial pneumonia I was unaware that I had.  One of the only memories I have of that early 4am event, was the look on my daughters faces as I was rolled by.

As I talked to my fellow survivor, one of the things I wanted to do, as I do with others in our situation, is to share our experiences, as to offer some sort of comfort to the stressful event soon to take place.  I encouraged her to focus on the surgery.

I had spoken with both of my daughters this evening, to gather their perspective on what happened those two time periods, the second time period they were five and seven years older.  Neither really remembers anything from my heart surgery.  And all either of them really remember of the second episode, was all the policemen and paramedics in the house.  It was never a thought to them that I would not come back home, though it was unusual for me not to be home.

For the second time, I had been apart from my daughters.  And this would happen again several times.  It never got easier.  Just as my fellow survivor feels I am sure, our children mean everything to us.  Fortunately they were at an age, where they really did not need to know or understand how serious everything was.  All that mattered to me, was that they knew I would come home.  And with every time something happened, this was how I handled it.  Each time, they believed I would come home.

Late in their teenage years now, they are learning more about my health history, and the origin, my battle with Hodgkin’s Lymphoma and the treatments used to save my life.  They can handle the details as I have given them in small amounts, and not in vivid detail.  As adults, they will learn the seriousness of the things I face, because as they will be my medical proxies, it will be important that they know all the details.

My daughters do not recall anything from my heart surgery, and have very few memories of the second event.  And I am glad for that.  They have witnessed enough with me in the hospital.  They know my situation is serious.

More importantly, they know that they are the reason that I keep fighting when faced with these challenges.  My divorce has caused quite a bit of separation, and while I do miss every moment I wish I could have with them, it pales in comparison to the emotional pain I felt back in 2008 when I thought I would never see them again.

Yet, here I am.  Another year closer to seeing them graduate, hopefully go to college, and perhaps start a family of their own.  Something back in 2008, I never thought I would see.

Post Navigation