Paul's Heart

Life As A Dad, And A Survivor

Archive for the category “Education”

Chemo – Day One, Part 1


This post continues my journey towards 30 years in remission of Hodgkin’s Lymphoma.

The time had come.  After eleven months, several diagnostic procedures, and failed radiation treatments meant to avoid this day, it was finally here, my first day of chemotherapy.

I have always been a planner.  Prepare for the worst, hope for the best.  I had read up on all the drugs that I would be injected with, and the potential for side effects.  I knew the two side effects that I had seen so many times in movies and on television, nausea and hair loss.  All I had to do was get this thing started.

One of my biggest faults, is that I am always considerate of others before my own needs.  And this day was no different.  And I did my best to make sure of it for the next eight months.  My attendance at work was rarely impacted during my radiation treatments, to the first hour of each morning, allowing me to work the rest of the day.  For my chemo, I had to plan differently.

I would receive seven different drugs, four during one injection, then a week later, a second injection would be given with the other three drugs.  My appointment was the last one available on a Friday, meaning I would only miss an hour of work, twice a month.  Expecting to be violently ill following the treatment, I would have the weekend to recover, as the time period between the injections was meant to do just that.  And that would be the plan for eight months.

I woke up that Friday, made my breakfast and lunch.  And in spite of me not having any appetite for obvious reasons, I knew the poisons that my body would be taking in, and I needed to take in as much nourishment as I could to give me my best chance of getting through these treatments.  It was not until past noon, that I was no longer able to distract myself from my appointment in less than three hours.  At 2:30pm, I punched out of work, got into my car, and drove to my oncology office.

My routine at the oncology office was pretty much the same.  Go into the lab to have blood work drawn, then go into the exam room.  Today would be different.  From the lab, I would go into the chemotherapy room, where there were two chairs for patients.  I would never see anyone else in the other chair my entire time though I knew I was not the only patient being treated.  It was a very plain room.  You could see outside the windows to the hospital across the street.  Other than the supplies in the room, it was going to be just myself, and my oncology nurse, Brenda.

For those that have never seen what a typical chemotherapy suite looks like today, these pictures show that.  The room is bright and large, filled with other chairs for several patients, all being treated.  There is entertainment by visiting troubadors and televisions, and visits of the non-human variety meant to bring a little cheer into such a dismal environment.  There is even an aroma of food as patients actually eat while receiving their chemotherapy.

But I did not have that relaxing environment to get through my treatments.  Instead, I had been reading a book called “Positive Imaging” by Norman Vincent Peale.

The book emphasized that getting through difficult situations, we possess a power to help get us through our difficult times, by imagining not only the success, but how we get to that point.  And I was going to use that same thinking to get me through my treatments.  My goal was to not only imagine myself finished with treatments and in remission, but to even picture the chemotherapy drugs fighting each and every cancer cell.

To help with that process, I went to this appointment, and all the others after it, with my Walkman.  For all of you too young to know what this doohicky is, back before you had the Ipod and MP3 player, you had this box that played cassette tapes, and later CD’s, again, I know you may not know what I am talking about.  So let me make it simple.  It played music.  But not just any particular music.  I supposed I could have put soft and mellow meditating type music into it.  But after reading the book, I wanted fighting music playing.  If you could work out to it, fight to it, it was on there including “Eye Of The Tiger” and other Rocky soundtrack music.  And for good measure, I even put this song on there…

Why “Pacman Fever?”  Because every time the song came on, I imagined the chemotherapy eating up the cancer cells just Pacman gobbled up dots.

Yes, I would have had a much easier time getting through my treatments with chemo suites of today, but I did what I could, with what I had.

My oncology nurse, Brenda, came into the room, with her prepared syringes, saline bags, and IV line.  Her face was sullen which I was not used to seeing that way.  She was in her mid-40’s, I believe, short and frosted hair, glasses, and always had a pleasantness supported by her smile.  She put her tray down on the table top next to me, and pulled up her stool.  At this point is where she told me that she had a son my age.  And now I could understand her sullenness.  And just like I thought of my co-workers, my fiance, my family, I had another person that I could not let down.

The IV line had been inserted into my left arm.  It was time to begin.

Father/Daughter Moments


I am truly blessed.  And in spite of all the health issues I deal with, I have gotten to enjoy so many things with my daughters throughout their childhood.

From reading to both of them, learning to walk and ride bicycles, and helping with homework, I have so many memories us, and how they have grown.  Both enjoyed sitting on my lap, while I read to them.  Once they realized the world that awaited them, by standing on their feet, they quickly learned the importance of putting one foot in front of the other.  They learned balance from learning to ride a bicycle.  I am proud to say that both have now reached a part of their education, where it is not so easy anymore for me to help with their homework not only because of what they are learning, but how.  Both enjoy the challenge of their education and do not look for the easy A’s.

We are coming around the homestretch of their childhood now.  And there are two things that are coming to the front where my input as their father is going to play a vital role, boyfriends and continuing their education after college.

As much as I cringe when the thoughts of dating come up, I believe I have given them not only a good example of how they should be respected by someone interested in them, but I believe that they both have the firmness to stand up for how they want to be treated.  They have had a few other good role models in baby sitters when they were younger who demonstrated the importance of focusing on their education and their values.  I have heard the “boyfriend” word mentioned a couple times so far already, and I have taken it in stride.

But an even bigger decision is coming right at them, very quickly.  And that is what to do after high school.  Sure I am biased and will say that both have a bright future ahead of them.  It is one thing to say that I will support whatever they want to do after high school.  It is another to make sure that they have the opportunity and guidance to do that.

Making those decisions is not something that can be done last minute either.  But once an idea is thought of as far as future, then I have figure how to get there.  Both have pretty good ideas of what they want to do, and each will have their distinct way of getting there.  One’s talent may take her as far as she wants to go depending on the balance between natural ability and what is expected.  She is an artist after all, and does not like being told what to do with her talent.

But my other daughter is expected to take a different route.  And I remember as a teen myself, when it came to figuring what I wanted to do when I grew up, we either had the idea, or maybe our guidance counselor at school might get involved.

The other day, she showed me just how much thought is going to go into, to prepare her for what she wants to do, even as far as specializing.  And to help her with that, something we did not have way back, besides the internet, is a web site for the Bureau of Labor Statistics (www.bls.gov).  This by far is one of the best tools to help a parent and child figure out what is going to be required to achieve their future occupational goals.

The web page not only lists the type of job, but the average salary, the entry level of education, and as you go further into it, descriptions of the work environment, how to get hired, state and area requirements (some vary from state to state), education required, as well as other resources of who to contact for more information.  Also just as important, the job outlook for the particular field.

My daughters do not use me much for homework anymore, except when it comes to the occasional need for proof reading things.  And as I have stressed to them, paperwork completed from now on, needs to be the best they can submit.  They see the difference that their decisions and actions will make.

I wish I could keep them young, but that would only satisfy my selfish happiness.  I enjoy being their father.  I am proud to be their father.  And I cannot wait to see what lies ahead for them as I am counting on being there when it happens.

Preparation For Chemo – Part 4 – A “Coaching” Change


continuing on with the “30th Anniversary” of my remission from Hodgkin’s Lymphoma

To recap from the last post, I had tons of questions.  So many in fact, the doctor refused to answer any of them, which led to the nurse who would be administering my chemo, to be the one to answer them.  And there were a lot of questions.  And Brenda took the time to answer each and every one of them.  But it was not any particular question that prompted the next and unexpected issue.

I am getting really ahead of myself in this post, or series actually, but I must.  Because looking back, I now realized that Brenda was more than just my chemotherapy nurse.  And without going too far ahead, it was during my first chemotherapy treatment, she would reveal to me something very personal, she had a son my age.  No, I was not the son.  But, my being her patient, gave her an understanding, which I felt resulted in me receiving not just a nurse’s care, but a mother’s care as well.  You could see it in her, it could easily be her son in the chemo chair instead of me.

The combination of Brenda’s professional skills and her motherly instincts, left her with a concern following my interrogation.  She could tell that while I had all my concerns answered, my mind was still not at ease.  But this issue would be above what she was trained to handle, and it would take more than a “mother’s” support.

This is a current picture of the campus where I was treated.  The building in the lower right corner, served as my oncologist’s office.  Brenda had recommended that I travel across the street to the main building, to the 9th floor (I believe that I recall that correctly), which was referred to as the cancer floor.  I was to ask for a man named “John.”

The one aspect of treatment and survival that nearly every one of us underestimates and values, is emotional support, therapy, seeing a shrink.  The stigma of being unable to handle something emotionally, or worse, that we might be crazy, is what keeps many from getting the most important aspect of their care, emotional support.  And my first attempt at getting any support in my cancer journey, through my church minister had failed miserably.

I got to the ninth floor, clearly this was the cancer floor, or so I had assumed from all of the hairless heads I was seeing walk past me.  I approached the receptionist, and said that I was there to see John.  The receptionist asked me to have a seat, that he would be with me momentarily.

From the archway to the office areas, a large figure came towards me.  All I could tell was that he barely cleared the archway, from a height perspective.  I do not consider myself tall at all, at 5’7″.  He clearly stood over a half of a foot taller than me.  He reached out to shake my hand, only to engulf my hand, as if some sort of armor, but not armor for war, but to protect.

“My name is John.  You must be Paul.”

We walked back to his office.  John offered me anything to drink or did I need anything else to make me feel more comfortable.  I took that as the green light to just unload.  And I did.  For nearly an hour and a half, I spilled my guts to a complete stranger about my fears of what I was facing, from the treatments to the mortality.  I broke down several times, something that actually brought me some relief as opposed to the continuous bottling up I was accustomed to, protecting everyone else around me.  With John, I could release this crap.

The funny thing is, it was not all the things that I listed that I was afraid of, or concerned about dealing with, there was still one thing that I was struggling with, and it was John that helped me to realize it.

I was not happy with someone in my team.  And I, as a member of my treatment team, needed to deal with it.  But as a patient, what I was about to decide had never crossed my mind.  But John helped me to realize just how important my feelings were to my treatment.

I came to Dr. M. because he save my grandmother’s life from her battle with breast cancer.  At the time, that was the most important consideration, his obvious success.  But just as important as Dr. M’s record, was my comfort, which I felt was not being met.  John’s suggestion nearly knocked me on the floor.

“Would you like to switch doctors?”

I could not believe what I was hearing.  Would it even be possible?  What if it could not be done, would Dr. M. hold it against me, thereby possibly impacting my results?  Would the next doctor see me as just a pain in the ass and could I possibly be treated worse?  And then how much time would I have left?  Remember, Hodgkin’s is best treated as soon as possible.  Would I have to start all over with diagnosing and staging?  All these questions, and before I could ask John, he already had an answer for me.

“You could always switch to a different doctor.  Dr. V and Dr. P are available in the same practice and can take over your care without any interruption to the plan.  Would you like me to reach out and try to arrange this for you?”

I could not believe what I was hearing.  This was like a football owner firing the coach the day before the Super Bowl, exactly for just the reason I was changing doctors, just because I did not like him.  I had seen both of the other doctors during my staging process, and really, up until my pre-chemo appointment conflict, I liked all three doctors.  But both Dr. V and Dr. P were younger, and definitely more personable.  I sat there in disbelief as John lifted his phone and made the call over to my oncologist’s office.  And as simple as that, I had a different lead oncologist, and my chemotherapy treatments would commence as planned.

One final breakdown, of relief.  John came over and said, “it’s okay.  What you are feeling is totally normal.  You did the right thing by dealing with it.  You are as much a part of getting through this, as your doctors and your treatments.  Hopefully now, you can focus on getting through this.  And any time you need to talk or need help, about anything, come over and see me.

There was a huge relief that came over me.  I would not allow myself to feel bad, kicking one doctor to the curb, just because I had feelings.  This was important to me.  And as a team member, I made the right decision.

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