Paul's Heart

Life As A Dad, And A Survivor

Archive for the category “Side Effects”

Trade Places With Me


My health history is well documented on this blog (much to the chagrin of many).  I have always been open about things because I want to do what I can, to show others, a) they are not alone, b) their issues are real, and c) if possible, how to find help.  But my openness has also been about hopes, as unrealistic as they may be, of catching a break from those who felt it was their place to question my health, as if my health issues personally affected them.  This type of relationship caused much stress over my later years, as some did what they could to eliminate me from their lives by ruining mine.  And this resulted in a lot of stress.  So, I am going to try one more time, and undoubtedly I will “bang my head against a brick wall” again and again and again, because I really believe at some point, everyone will finally “get” it.

I read “double” local news, where I live, and where my children live with their mother (another state).  An all too common situation, which I have experienced as well, was reported on by the local newspaper, The Reporter.  An incident occurred at the King Of Prussia mall when a mother had taken her 7 year old son to see Santa Clause.  Yes, you guessed it, she parked in a handicap spot.

When the mother came back out to the car, a message had been written in lipstick on her window, “UR not handicap.”  Someone who had made it their business to monitor handicap spaces saw an apparently healthy woman and a child climb out of a vehicle parked in a handicap spot, and was not going to let this criminal get away with it.

Here are the facts, as reported by The Reporter, not that it was any of the intrusive and offensive bystander’s business.  The boy has a disease called Batten disease.  He is blind, and “slowly losing his motor skills.  Most children with the disease don’t live to their teen years.”  So there you have it parking lot vigilante.  Great job!  Your judgment made things right because you felt it was your business.

Chances are, nearly everyone has seen someone pull into a handicap spot and wondered, okay, what exactly is their  handicap.  First off, it is none of our business.  But it is the abuse by a few, that we feel compelled to enforce the use of the special parking spots.  We do not have that right.  And on top of that, our intrusiveness can often make a situation worse.  We do not have the authority, or the ability (skills to discover lack of an actual disability), to make someone using a handicap parking space, our business.

I know many people who go through life, “hiding” their disability as best as they can because they do not want to experience scorn, discrimination, or worse, ridicule.  Since my declaration of disability occurred back in 2010, I have experienced my share of the “dirty looks” and abusive comments.  I actually do possess a handicap placard, and it is a permanent one.  You see, my health, albeit gradual, is getting worse every day.  Here comes the argument.  “We all get older and our health goes down hill.”  An accurate statement.  But how many of you have a head start in this process?

As a long term survivor of Hodgkin’s Lymphoma, I was treated with radiation four times the life time maximum exposure of ionized radiation, and toxic chemotherapy that has caused progressive damage to many parts of my body.  Do not take my word for it.  This was the diagnosis by one of the top doctors at Memorial Sloan Kettering Cancer Center, where their survivorship clinic follows long term survivors like me.  The date on my birth certificate states that I will turn 52 soon.  In actuality, my body is more similar to that of a 75 year old.

I know, this picture does not look like a 75 year old.  And honestly, it was taken around two years ago.  But because over the years, after viewing people’s expressions when they hear even just some of the health issue I have to deal with, like even as little as one (I have 13 confirmed diagnosis of a major classification – the doctors are not dealing with the lesser issues), I developed an attitude that I need to “hide” my issues from many people, because they simply cannot handle it.

But I do have a permanent handicap placard for my car.  I do not use it often, perhaps maybe 5% of the time that I am out.  There are many factors that determine if I use it from weather, activity, and how I am feeling that day.  But you will never know, because I do not complain to anyone.  Anyone close to me has experienced moments around me, when my issues have been too much for me to handle at a particular moment.

I have learned not to react impulsively by someone ignorant enough to tell me I do not “deserve” to park in a handicap parking space.  First, I realize that the first thing that is driving the busybody is a jealousy that I might have gotten a closer space than they had to park.  I do not like using these spaces myself, but if I do use it, there is a reason.  And I will let you know very graphically if you decided to make it your business.  I am not proud of my method, but I will make sure that you think twice before confronting someone else by pure shock and guilt.

I will start by pulling open my shirt to expose the eight inch scar on my chest and tell you about the open heart surgery I had.  Follow that up with my restrictive lung disease that makes it difficult to breath in certain weather conditions.  That is just the start, because I will unleash every one of my health issues on you.  By the second issue, my lungs, I watch the person cower in shame.  I am not proud of what I have done.  But they started this.  But was it their fault?  They had no idea about my heart or my lungs?  But by the time I am done, they sure as hell know why I am parked in a particular spot, and it is because I have to, not because I want to.  Hey, anytime you want to trade positions with me so that you can park closer?  Let’s do it.

I have many friends with internal issues that qualify them as “disabled” or handicapped.  Those issues are internal!  That means you cannot see them.  Sure, there are people who will abuse the system, but those who actually need the assistance do not deserve or need the added stress from a false accusation.  It makes no difference if a person is climbing down from a monster truck, or off the ramp of a van in a wheel chair.  It is none of your business why someone is using the handicap spot.  And having experienced it first hand, you do not want to know why I have used one.  You most likely will not want to handle it.

I hope that the ignorant ass that scribble on that mother’s window in lipstick at the King Of Prussia mall feels as low as a human can feel, having to climb a ladder to kiss a snake’s behind.  The mother has enough to deal with having a child that will die as a child.  It does not matter if the child does not look the part.

Donna’s Wish


I am so pleased, as I and others deal with the sorrow, as per the wishes of my friend Donna (who recently passed away from complications of her late effects from treatments for Hodgkins Lymphoma), and her family, husband Leo, and daughter Jasmine, that in leui of flowers, that a donation be made to a charity that would continue Donna’s efforts in support of those battling life after Hodgkin’s Lymphoma.
That charity is Hodgkin’s International. There is a “donate” button along with Donna’s story.

To donate in Donna’s memory, and to see what HI is about, please go to Hodgkin’s International at http://www.hodgkinsinternational.org

Thank you in advance.

Donna – As Genuine As Could Be


I do not even know where to begin.

This is a photo of a mother, wife, a fellow adoptive parent, and a fellow cancer survivor.  Her name was Donna.

Donna and I first met, well over a decade ago, on an internet listserve for long term cancer survivors, which we both were.  She had been treated at a very young age for Hodgkin’s Lymphoma with an extreme amount of radiation therapy, though considered standard for the time.  Those treatments caused progressive side effects over the decades, in the beginning unknown, but later on life, not only aware, but severe in nature.  When we were first introduced to each other, my issues with late effects were at the unknown stage, so it was not late side effects that led to open conversations.

Donna and her husband had adopted a daughter from China, named Jasmine.  Donna had seen that in the signature of my posts, I had adopted daughters from China as well.  From there, since we could not share photos on the listserve, and it really was not proper etiquette to contact someone from the list on a personal level, Facebook came along.  And from there, that is where our friendship grew.

We shared a lot of photos of each others’ daughters.  We shared a lot of stories.  One thing that stood out in my mind, was when “Jazzy” as her father calls her, at a toddler age, was showing off for a video camera entertaining with a Brittish accent having a conversation with her mother.  It was hysterical, and very authentic.  And this friendship grew, as we watched each others’s girls grow.

In 2008, our friendship took a very hard turn.  My late side effects were suddenly brought to light in a huge way, emergency heart surgery.  I had been aware of Donna’s issues, though she rarely publicly spoke of them.  And if she did mention them, there were bad enough at that time for her to do it.  She was one of the first survivor friends to reach out to me, offering encouragement not only on my recovery, but with the new direction my survival was going to take.

Now, we were not just exchanging stories on our daughters, but now, seeking each other’s support for suggestions on how to deal with certain health issues, offer encouragement during a side effect event.  And for both of us, over the next several years, we both would be dealing with several events.

During this time, we both had family to take care of as well.  And we did most of it without skipping a beat, protecting our young children from knowing the harsh realities we were dealing with.  And for that, we would find our way back on Facebook, sharing more photos, more  fun times, more memories.

This father/daughter duo served as inspiration to me.  Donna would constantly share the musical escapades of her husband Leo, and daughter.  Performing here, performing there.  Such a great bond.

That is not to say or friendship did not have bumps.  As the title of this post suggest, “As Genuine As Could Be,” Donna was very genuine.  It was only one subject matter that could fire up our conflict, but one thing was certain, we both could stand our ground.  We would trade “comments” back and forth trying to convince each other that our opinion was not only accurate, but correct, in our opinion.  And let me tell you, that determination and strong will, definitely played a role in her cancer survival.  After we exhausted our argument, we would return back to what mattered to both of us, our daughters, and our survivorship.

I cannot imagine what Leo had gone through as a spouse dealing with someone facing these constant health crisis that would keep popping up.  I was a caregiver for my father, but as a spouse, I am certain it was different.  But I know that Donna loved Leo very much.  They were in photos constantly as a family.  But he also had to be there, to make sure that if Donna was unable, to relay information to medical personnel about Donna’s health history.  For better or worse, in sickness and health… their marriage endured.  And that is not something easily done without dealing with the extreme health issues of a long term cancer survivor.

I often find myself, ridiculed by some of my friends who feel that surrounding myself with others who have gone through what Donna and I have gone through, to be part of internet support groups that deal with late effects, can have an impact on my psyche as far as having a positive attitude, can only lead to living under a dark cloud.  As is proven by my friendship with Donna, nothing could be further from the truth.  Donna is one of perhaps a handful of fellow survivors still alive from when I first came across the internet.  Given my health, I know that does not bode well.  Regardless of her side effect issues, she was too young to leave this earth.  She is yet another parent I know, survived by such a young child.  Again, I cannot begin to imagine the grief that Leo is going through, all the while, having to make sure that his daughter’s emotional needs are taken care of.

I have written that I do not grieve well, or even properly.  But if there is one thing that will always stand out in my mind about Donna, she gave of herself, before for herself.  If I was dealing with an issue, she offered me guidance, all the while keeping her current issue silent.  Yes, there were topics that she definitely felt strong about, but it did not stand in the way of friendship.  More importantly, she was a great mother, and a great wife.  And she was a great friend.

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