Paul's Heart

Life As A Dad, And A Survivor

Archive for the category “Education”

Starting Over


(photo of the Hindenburg disaster courtesy of Wikipedia)

This is probably the most confusing way for me to start a post, contrasting both the cover photo with the title. But I do not have permission to use the photo I would rather use. This photo does have some relevance though.

My first ever family doctor, was a kind and soft-spoken elderly gentleman. In fact, his office consisted of only he and his nurse. His office was in a cordoned area of his huge Victorian house. There was an exam room, which tripled in purpose as a lab, and pharmacy area. Outside the room was the waiting room, which was actually a hallway. At the end of the hallway, was the entrance to the house. I never saw any members of his family beyond that door, ever.

Sitting on the bench, waiting to be called in, looking straight ahead in front of me, on the wall, was a framed cancelled ticket, for that final and fatal flight of the Hindenburg. My doctor, an accomplished flyer himself, was supposed to be on that flight. I do not remember why he was not on it. But he would continue being my family doctor, practicing medicine fifty years. His obituary was filled with acomplishments, one after another, a major pillar in our small town.

Having to find another family doctor, I discovered that the term seemed to change to “family practice,” or general practitioner. I began to see a new doctor for a few years after which a new doctor had joined his practice. He would retire, turning the practice over to that other doctor, now only my third doctor, and who I thought would be my final family doctor, now referred to as a primary care doctor. She would be my only family doctor for the last four decades.

Now the title of this post may be starting to make sense, because here is the deal, she is retiring, and that means, that I will need to find a new doctor once again, something that I do not have a lot of experience in, and for good reason. But if I am being honest, I really did not expect to see this day, at least not on my end with the complicated health history that I have. But I digress.

For the first half of our patient-doctor relationship, I took it pretty easy on her. My Hodgkin’s Lymphoma treatments were over, and other than a seasonal allergy shot I received, I rarely if ever saw her. In fact, on one rare occasion, after tangling with some poison sumac, I showed up at her office, all in the office seemingly surprised to see me so unexpectedly, the comment was heard, “it has to be something bad if Paul is here like this.” I was covered in huge blisters, painful, due to the sumac exposure. And the doctor knew what needed to be done.

There was also another situation that came up in 2003, when I was injured on the job. As many employers are prone to do, though it was definitely a work-related injury, the insurance company handling my claim, denied my case. And it was during this process, the doctors I was forced to see, missed, or ignored the actual injury. But once I was denied my claim, I was allowed to seek medical attention outside of the workers compensation process, and guess what, my family doctor ordered whats workers comp would not, an MRI, and found out that I did indeed tear a cartilege in my wrist. And this was not just a regular tear. It was only the kind of tear that could come from a violent action, job related, such as jack-hammering, or playing hockey, a heavy torqueing of the wrist. My doctor knew me well enough, I did nothing in my personal life that could cause that severe an injury. Nine months later, I won my claim appeal. And it was because of my doctor’s persistence and knowledge.

The most consequencial diagnosis from my doctor would come in 2008, when I made just a random phone call to her, with an “annoying” complaint involving a chest tightness in the upper left part of my chest. It was a temporary thing, but it happened nearly all the time, and to my recollection had been happening for months, when I would begin to do anything physical. I was only forty-two years old, and though my insurance company objected to the test my doctor wanted performed, based on her assessment of my past cancer history she pushed forward ordering a nuclear stress test (admittedly I had no idea what was being sought), thirty-six hours after that test had been stopped (the technicians had seen something), I was on an operating table, having emergency heart surgery for what is nicknamed a “widow maker,” a major heart blockage which normally results in death, hence the nickname. The cardiologist even went as far as to say, “it wasn’t a question of if you were going to die, but when.” You want to talk about getting someone’s attention? I had this symptom for as long as four months that I could remember. And had it not been for my doctor, her knowledge of medicine and her patient, I would be dead. That is not an overstatement.

Over the next seventeen years, as it was determined that my heart issue was one of many compromised conditions related to late developing side effects from the treatments that put me in remission for Hodgkin’s Lymphoma thirty-five years ago, my doctor would play one of two key roles in my team of care providers for these issues and more. And it was her care, her refusal to give up if I complained of an issue, because she knew I did not reach out to her unless it was that uncomfortable, she and my long term cancer survivorship doctor (located at Memorial Sloan Kettering Cancer Center), made sure nothing was ignored.

She has been my family doctor for four decades, nearly forty years. I can honestly say I have had the best medical care, the best health advocate, a patient could ever hope for. And just as in the case of my first doctor, who adorned his office with personal effects such as the ticket for the Hindenburg, over the decades, my doctor kept her office and waiting rooms with that same family and personal feeling. I loved seeing photos and artwork from her children, watching them grow. And in one rare moment, I asked a question of her, a personal question, but important. I have never doubted her as a doctor, and never thought twice about why she became a doctor. But what was it that made her go the “extra” that it sometimes took with her patients, especially when it came to issues like I deal with, not covered in medical text books, or at least not until recently. Her answer brought me to tears, a personal impact that taught her to listen, truly listen to her patients, and most importantly, believe them. But it was definitely why she was the doctor that she is. Boy was I lucky to have her.

I am happy for her. She has definitely earned her retirement, though she is just a few years older than I am, I am not able to call that retirment age. But it brings me to an unfamiliar crossroad, one that I have not crossed in four decades, finding a new primary care doctor, my new health advocate. The bar has been set extremely high, combined with what I know and understand about my health, I will be expecting a lot from my next doctor.

So I am… starting over.

Among my fellow survivors, I have seen the struggle is real, finding even just one doctor who gets it, who understands “late side effects” from exposure to high doses or radiation and toxic chemotherapies not used in decades, not researched, and quite frankly, we were not expected to live long enough to even know what could develop. But we have lived long enough, and many of us have developed these issues.

I, we, need doctors that listen to their patients, taking the time for the “brick layer to explain to the engineer”, the patient to explain to the doctor, what the doctor may not know or be familiar with. And then we need that doctor to have the persistance to push for tests and answers, so that treatment, whether curative or maintainance, can be administered. And when pushback comes from the insurance companies or corporate, because our situations are not written in the books, we need to know that our doctor will fight back because without their voice, we will die.

Is there another doctor like my previous doctor out there? Perhaps. But if my fellow survivors are any indication, it will be more like searching for the proverbial “needle in a haystack,” than what should be an easy Google search locally.

I am happy for her. I am excited for her to be able to enjoy time with her family, a gift that she has given to me many times over.

A New Normal


There are common thoughts in the journey of cancer and survivorship. From diagnosis through treatment, I know that all that I wanted to know was long term survivorship possible, beyond the five years that I constantly kept hearing about? Strangely, once I completed my treatments, combined with achieving the status of remission, my thoughts quickly turned from long term survival, to when does my life get back to what it used to be, “normal.”

While the cancer experience is definitely physically demanding, enough attention does not get paid to the emotional and mental toll that is taken on the patient. Sure, there is fatigue, fear, doubt, stress, paranoia and more that swirl around in the mind of someone going through cancer. One thing that we do not realize happens during the time from diagnosis through treatments, unbeknownst to us, we lose something very important to us. And we do not recognize it until after we are done with treatments, yet it plays a very important role in us moving on in our lives, in our survivorship, control. We go from doing what we want, when we want, to, you have to be here at this time, we are going to do this at this time, and a patient has no control of that. Decisions are no longer made by the patient, but by those providing the care. And it is in our best interest to do as they are recommending if we want to reach remission.

When we lose things, such as our car keys, our wallet, material things, it produces an inconvenient anxiety. When a loved one is “lost” or passes away, we mourn or grieve. The loss of control then, I feel would fall in between those two extremes. Without any thought, once treatments are over, the “keys” are handed back over to us, and we are supposedly back in control. But why does it not feel that way then? If the treatments and the tests are done, when does it start to feel “normal” again?

Control and normal are two different things, yet combined create an interesting dynamic, an experience that must be dealt with, and accepted. Soon, we realize what that loss of control did, and what it took from us, normalcy. And once we realize what we considered “normal”, and that particular “normal” is gone forever, we soon come to terms, this permanent loss, is similar to the loss we experience when someone passes, and must be grieved. We need to give ourselves the chance mourn what we looked at as what was normal in our lives, before the cancer.

Unlike the passing of a loved one, we have a hope or even a second chance with remission at normalcy, but something we in the circle of survivors call “the new normal.” As a cancer survivor, we all get this new normal, and it is exactly that, new and whatever we want to consider as being typical in our lives going forward.

What exactly is normal? What do you consider normal? What makes things or life normal? If normalcy is based on never seeing doctors again once in remission and totally forgetting you had cancer, nope, not going to happen. That normal is gone. Over decades, medicine has finally recognized late developing side effects as a reality, not necessarily for all, but for some, and the problem is no one knows who will develop these late effects. Therefore, ALL cancer survivors should continue following up with their primary care doctors once they are released from their oncologist, with guidelines from the oncologist what issues to keep an eye out to potentially occur, not definitely, but possibly. That is a new “normal” especially if you are not one to have ever seen a doctor regularly (besides the oncologist).

Aside from the medical new “normal,” I have come to realize that each day brings a new “normal.” And because I am someone who has a variety of late developing side effects, the “normal” for that day depends on if any of those effects are gathering attention or not. What I have found, and actually accepted, is that this is okay. Another new “normal” I have been able to achieve, is how I deal with stress, much better.

Perhaps my most important “normal” however, are my daughters. Becoming a Dad, now decades ago (a surreal thing to say as a cancer survivor), has been the most normal part of my life. There are no quotes around the word normal this time, because you can quote me on this, for me, becoming a parent has been the best kind of normal I have gotten to experience. And each day, I look to build on that normal.

The truth is, normal is what you make it. And that is what makes it “new” after a battle with cancer. Because now, you, the individual are the one deciding what is normal.

Happy Father’s Day


Happy Father’s Day to all who are celebrating today, and my heart goes out to all of those who recognize this day, to remember their Fathers, no longer with them, and for those, who through no fault of their own are kept apart. At one point, I checked off all three of those boxes, so I understand all the emotions involved.

As a Dad of two amazing daughters, this is my day, bigger for me than Christmas, birthday, even my once favorite Halloween. But the biggest part of my life, my legacy if you will, is having made the decision, to be responsible for two children, to teach them values, morals, right from wrong, all the while making sure they learned in school, and became responsible adults. Of course, as you know reading “Paul’s Heart”, this has not been easy with the variety of health issues I have faced as a cancer survivor. But this I know, I do not take any day for granted, and I celebrate every new day that I get with my daughters.

But as I said, I checked off more than one box when it comes to today. I lost my Dad to lung cancer eleven years ago, he was just ten years older than I am now. He was not alive to see what I went through as a Dad dealing with the family courts in regard to the relationships with my daughters. Of all the things unresolved with my father (my parents divorced when I was three years old), my Dad was only aware of the beginning of my own divorce and custody fight, as that was when he was just diagnosed. I could not throw this issue on him, while I dealt with both simultaneously. I am hoping, that my Dad is looking down on me and his granddaughters, and seeing how well things turned out with the my daughters and I.

The link above is for a performance for a special piece that I wrote in tribute to my Dad.

However you are recognizing today, I hope it is a good day for you.

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