Paul's Heart

Life As A Dad, And A Survivor

Archive for the category “Family and Friends”

Save A Life – Share This Post!!!!


These are copies of a laminated card I carry in my wallet, and reflects the warning on my med-alert bracelet.  I am asplenic, in simple words, I have no spleen.  Like many others, and for any reason besides cancer, a person could be left without a spleen.  And if that is the case, that means that you are at an increased risk for infections and illnesses, including developing a fatal condition related to sepsis, which I have dealt with twice.  And were it not for this card, and the quick thinking of my doctors, I may not be here today.

I am a member on many pages related to Hodgkin’s Lymphoma, but as I stated, being asplenic is not just related to cancer.  Trauma such as a car accident, another illness, could result in the loss of your spleen.  And the chances are, that you know at least one person in your life, without a spleen.  And if you do, this information will help to save their life.

I received this information over ten years ago, when I met the doctor who is dealing with all the late side effects from my cancer treatments.  This information is given out by the survivorship clinic at Memorial Sloan Kettering Cancer Center, so this is information that is very important, and proven.

Please share this post, encourage the printing of this card, or even typing it yourself, but keep it.  If you end up with a fever over 101 degrees, get to the emergency room.  They need to check your lactic levels which will either confirm or deny sepsis.  With sepsis, it is a matter of hours of saving your life.  The more knowledge and tools you have, the better chance you have.

Over the last decade, I have known too many who have died from sepsis.  Patty Duke, former child TV star, died from sepsis.  The attention to sepsis lasted only days, yet every day, so many patients face sepsis, and unknowingly, pass away with the cause not determined, likely to have been sepsis.

Timing is important.  Share this post.  If you know someone without a spleen, give them this information.  They will be glad you did.

“Whose Life Is It Anyway?” Loss Of Control


I love the “Pirates Of The Caribbean” series of movies.  And there is not better picture to describe the way your life gets taken from your control, than when the two main ships were battling against each other, and dealing with the vortex.  This is exactly how it felt 30 years ago, staring down the diagnosis of Hodgkin’s Lymphoma, recovering from major surgery to “stage” my cancer, and the road that was going to lead ahead.

Under normal circumstances, we have our own control in the palm of our hands.  Sure, our employers and teachers can take some of that control away from us, because, well, it is an authority thing, and we have to do what they say in order to get paid or to achieve our diploma or degree.  But when we get sick, seriously ill, it is the realization that we lose all control, to our illness if it is serious enough.  Sure, we have a say in how we get treated, but ultimately, it is the doctor calling the shots.  Even the illness and treatments (along with side effects) control how we get through each day, if we have enough stamina to go for a nice afternoon walk, or barely enough to get a drink from the refrigerator.

The “staging laparotomy” for my Hodgkin’s did something to me that nothing had ever been able to make me do before, miss work.  Up until that point, I had never missed one full day of work.  Recovering from this surgery was going to mean I would miss an entire month.

That was not the only loss of control that I had felt.  At home, I was dealing with a new issue, being cared for, and being cared about.  I was not prepared for the “overboard” attention that I was receiving since my diagnosis.  It was overwhelming.  So much so, that instead of returning home from the hospital, I made the decision to “hide” away from everyone, staying at the home of my future in-laws.  I knew there that I would have quiet, able to regain my focus on what was ahead, able to get things back under my control.  Or so I thought.

This is an actual picture of my abdominal scar from the laparotomy.  Looks pretty neat and healed now.  But back in January of 1989, it did not look like this.  You see, one of the procedures during this laparotomy, unknown at the time, would leave me unable to fight infections as my spleen had been removed.  For a person with a normally functioning spleen, though the situation would be possible, it would be less likely, and less dangerous.  Only decades later did medicine realize how important the spleen actually was to the body to fight disease and infections.

In any case, a few days convalescing at my future in-laws, my scar, still fresh, had become infected.  Just when I thought I was getting my life back under control, my body decided otherwise.  But in my need for control, I took myself away from those responsible for my care, more than a half hour away.  The house was empty, as my fiance and her parents were at work.  I clearly could not drive.  I had no choice.  I had to call my aunt.

She was retired and in her early 70’s.  But she was the only one that was going to be able to get me to the doctor’s office, who wanted to see me right away.  I had not choice.  The infection was already bad enough, and could possibly go septic, something that would have the potential to kill me.

Unfortunately, it was not soon I realized, that the infection was not the only danger I was facing.  Now, I want to make perfectly clear, I am not making fun of any elderly drivers or making any commentary on if they should be driving or not.  But I will say without certainty, the infection was not the immediate danger to my health.  Oh, how I wish I could have just driven myself to the doctor’s office.

At some point, most all of us have had an experience driving along side, or in between concrete barriers while highway construction or repairs were being made.  Well, at the time, Rt. 309 was undergoing a major construction project, creating a new interstate.  What it meant was, while the first five mile ride was tolerable, as we approached the construction area, I now was afraid of something worse than cancer, my Aunt’s driving.

As the road shrank from three lanes to one, my Aunt brought her car to a complete stop.  This was to allow ALL other vehicles behind her, to enter the “cattle chute” before she did.  The reason why became obvious as she soon accelerated to 10 miles per hour, the pace she would keep for the remaining 10 miles on the highway, nervous of hitting either side of her car against the concrete barriers.

I eventually did make it to the doctor’s office, without any additional medical needs.  Though clearly I had developed a case of “white knuckles.”  The treatment of my incision did not take long enough to allow my nerves to settle from the journey there, before heading back.  I will spare the gory details of what was done, though even for someone squeamish like me, it was freakishly interesting to watch how he treated the wound.

On the way back to the house, it hit me.  I have no control of my life anymore.  I have a wedding in five months.  Nobody cares except for me and my fiance.  I have bills to be paid.  Nobody cares.  Be here on this day.  You need to do this.  Cancer was now completely controlling my life.  Even as I recovered from this surgery, doing nothing, no work, no driving, nothing, even the infection of my incision controlled me.  The following week I would meet with a radiation oncologist who would discuss with me, the prospects of radiation therapy.  And it would have to begin soon.  I had not control in any of my life anymore.

A Memory From 30 Years Ago I Will Not Forget


The last quarter of 1988 was one of the worst times of my life, though I really should not set the bar based on that.  30 years ago, I was facing cancer, Hodgkin’s Lymphoma.  I spent the last two months of the year, undergoing tests to determine just how bad my cancer was.  However starting 1989, was not going to be any better, because I was going to have to undergo one final diagnostic procedure, and it was going to be a big one, and recovery time was going to be an issue.  Up until this time, proudly, I missed very little time from work.  But this procedure was going to be much more extreme.  My memories of this time period are just as vivid today as they were back then.

30 years ago, actually a week ago, the Philadelphia Eagles visited the Chicago Bears in a playoff game, nicknamed “the Fog Bowl,” because of the strange weather phenomena that took over the stadium as fog engulfed and dropped into the stadium, making it nearly impossible for us to watch the game, let alone, the players to actually see what was happening on the field.  Today, 30 years later, the Philadelphia Eagles are again travelling to Chicago to play the Bears again in another playoff game, though no obscene weather is expected this afternoon.  But who knows?  No one expected that bizarre weather back then.

For the majority of my life, up until 1988, I was fairly healthy, only one minor surgery when I was six years old.  And already in 1988 I had received many new surgical scars, just to determine what stage of Hodgkin’s I was dealing with.  Now for those dealing with Hodgkin’s today, please, please appreciate the fact that you do not have to undergo this procedure, the laparotomy, to stage the cancer.  You get the PET scan.

What was especially frustrating for me, because I was more than aware of the concept of wanting to get this treated sooner than later, especially with my wedding coming up in five months, but if this was going to be the end all and determining factor of treatment options, why not just have skipped all of the other testing, and go right for this?  Of course, looking back, I can understand why now, but back then, it was just so frustrating.

For many of my readers who are long term survivors, this is deja vu for you, and for those who do not understand what exactly the laparotomy is, here you go:

There would be several biopsies performed through the 8″ incision on my abdomen.  My liver, some lymph nodes, and with Hodgkin’s being a cancer of the lymph system, the decision was made to remove my spleen.  Back then, the spleen was often deemed “unimportant”, able to live without, and to a degree, we can, I do, but it comes at a cost when it comes to fighting infections, and today, science knows this, and spleen removal is not done as often anymore because of those risks.

Up until this point, I had only one lymph node that tested positive for Hodgkin’s.  I was currently at stage 1.  Other biopsies and tests and blood work showed nothing.  Just as trying to play football in fog, getting the proper staging for me was just as difficult to do.  But just as there was a winner and a loser in that football game, my spleen was going to determine my outcome.

My spleen came back from pathology, fully involved with Hodgkin’s.  My staging changed from stage 1 to stage 3b (which meant there were symptoms with the staging.  The full diagnosis, staging, labeling, was “Hodgkin’s Disease, 3bNS”.  The NS stood for “nodular sclerosing” which is one of the types of Hodgkin’s classifying its aggressiveness, determining treatment options.

There was one thing I had to get through in the immediate moment however, THE PAIN!!!!!!  I had never had a major surgery like this before.  And now having been cut from my chest, just below my belly button, my insides torn apart to allow the biopsies, the pain was unimaginable.

As I continue through this anniversary journey, my memories are quite clear of what happened and how.

And though I am glad this scar is just that, a memory, it is still there to remind me of where I came from, and a reminder to all the new patients dealing with this diagnosis today of the progress that has been made.

And just as my body has healed from that surgery back 30 years ago, I am routing for the Eagles to be passed their memory of the Fog Bowl, and have my fingers crossed for a victory today to avenge that loss 30 years ago.

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