Who is Susan L. Schoenbeck?

Who is Susan L. Schoenbeck?

recently I received an email from a woman living in Arizona writing me that her doctor friend recommended me to her to contact me. I was flattered of course that my blog had become at least famous enough that someone from over the ocean took an interest in my blog living with post polio syndrome.

The woman turned out to be no one less than Susan L. Schoenbeck. An author of several books and a nurse trainer with a few awards of her work.She then wrote to me that she had just finished her book titled polio girl. An autobiographic story of her life, her family, her forefathers. And she asked me if I´d be interested to read it. Of course I said yes. I was interested what she would write about.hThe last book I had received from an author was about her dad, a doctor from Bulgaria who had polio. Strangely I found that I couldn´t read this book since it started triggering my own relation to my father. Which also had been tough though even he was very caring from his point of view and that was quite stressful and tensed at times too.

Anyway let´s talk about the Book Polio Girl – it only takes one. A book which is historical in both ways. In one that it describes the times when polio emerged in the US and historical about the time when it happened. And as written a few lines before the story takes you through her family in generations and also the fear polio created based on false knowledge and believes. And in synchronicity that this book is being published in the midst of pandemic times and its quarantines which also happened during the epidemic times of polio. The book also describes a panic stricken society living in fear and what reactions this fear causes way through the different classes of society and how this impacted even the treatment of being rich, poor or belonging to a different cultural background.

The way Susan Schoenbeck writes is very lively and vivid and takes you emotionally into the lives of polio survivors and her own story of course too. Susan Schoenbeck was struck by polio at the age of 7 month. A stage in life where a disease like polio would mark a whole family with a stigma creating  prejudices  by around social circles throughout her whole life. Read how a polio survivor like Susan Schoenbeck learned how to cope with all these situations in her life and how she successfully turned the lessons of polio into a strength by educating, teaching others and writing about her life and other important topics.     

Hopefully my sentences made you curious enough to grab this book and read it. Why? Because it is high time to get the message out there to understand that eradicating polio is not enough. Vaccines are necessary to prevent another outbreak of polio but as equal important is to recognize what polio survivors gave and are giving to society without asking anything in return but just a piece of recognition and respect for their contribution to society..

Do let me know what you think and if you are ready to read it. And if you have let me know what impact this book had or has on you – write to me!

Kay´s Polio Story starts 1952

Kay´s Polio Story starts 1952

I contracted Polio at age 2 in 1952 and was never very athletic growing up but had a fairly normal life. I married  at 21, gave birth to 3 beautiful healthy children and worked first as a cosmetologist then went in to school to become a medical lab tech.. I ran a full pediatric lab for over 17 yrs and my legs just simply couldn’t do it any longer. I’m almost 73, dealing with PPS and enjoy chatting with anyone else experiencing this problem.. aging is hard enough but we are tough and we WILL handle whatever life throws at us!

My birth mother shot and killed herself when I was 2 and my brother was 4 and apparently my biological father couldn’t handle a 2 yr old crying so he gave me to a relative and kept my brother. No one wanted me then because I was crying for my mother and my brother so I ended up with 5 different families I a period of 3 months. Somewhere along the line I contracted Polio and was finally placed with my birth mothers oldest brother and his wife. Their children were grown and they found themselves with a sick 3 yr old. The day they got me I was taken to the doctor, then to the hospital and then sent to a Polio Hospital nearly 70 miles away where I was a patient for several months. I always felt that I had been a great disappointment to them but I am a survivor not a quitter!! 💕 I’m not sharing my story for sympathy, just honesty, ….. thanks!!

Why is no one talking to me?

Why is no one talking to me?

Maybe the sun was shining, maybe the sky was covered with dark clouds.

All I really know is that my little body was burning with a fever that did not want to let go of its grip, and my head was breaking apart.

My legs do not want to carry me.  I am falling outside the toilet door. I do not shout because it hurts, I shout because fear drills its arrows into me. My mother and father come running.  Daddy lifts me up in his warm arms. I feel like a very small girl, miserable and ashamed. I, soon to be six years old, have not been able to stay dry. Daddy hums and rocks me slowly while he massages my legs which are completely red with heat.

Daddy says, “You will see kiddo, your legs have probably just taken a nap.  Soon they will be normal again. “

Dad tries to get me up on my legs, but it’s impossible. Mom comes in. She puts me in bed between cool sheets. She gently strokes my hair and puts Pelle, my cuddly fuzzy teddy bear, on my arm.  Everything feels so safe now.  

I hear them gently move around out in the kitchen. I understand from the sounds that mother is setting the table with coffee cups. These are the nice, yellowish ones with green stripes on them. My favourit cups.

What are they talking about? Mother’s voice sounds different.  “We probably have to call for a doctor now. A cold should not last that long and why did she fall suddenly? “, she pondered.

I never had time to hear my father’s answer, because the Sandman splashed his sleep glitter all over me, and let my feverish, aching body rest in a much-needed sleep.

I wake up to someone leaning over me, an older man, with gray hair, big glasses, and a bushy mustache. It feels like ice in my stomach. I wonder, “Who is he? Where are my mom and dad? “

Daddy asks, “Hi little lady, are you awake now?  This is a doctor who is going to look at you. Maybe he can help us get rid of the stupid fever. “ My father’s voice calms me down.   It does not feel dangerous to let the doctor take my temperature.  

The doctor notices that the fever is high, grabs my legs and squeezes them, and twist them. He does the same with my arms.  I shout out, “please Mom, make him stop, it hurts so much.”.   My mother stands behind the doctor, but she does not come to my aid.

“What’s going on? “, I think.  “Why is no one talking to me?”

The doctor mumbles something I do not understand. He disappears. My mother sits by my side, gently caresses my cheek, and smiles as beautifully as only she can. “You have to wait a little while sweetheart”, she says. “Mom and Dad need to talk to the Doctor a little, but I’ll be right back.”  I beg and plead for her not to leave me alone, but she leaves anyway.

I hear their voices in silent whispers. I wonder, “Have I been stupid? Should I be punished for peeing? But please, it was not on purpose.” I close my eyes. I do not want to see. I do not want to hear.  I must have fallen asleep for a while, because I am awaken by two men in white coats wearing strange masks over their mouths.

I scream. 

Behind them I see my mother standing with tears running down her cheeks.  My father is standing next to her with a protective arm around her thin shoulders.

They lift me up.  I exclaim, “Please, help me, they will take me!”  No one seems to hear me. I am carried away, then laid on a strange examination bed. It is so hard it hurts my back.   Then mother reaches me, she takes my hand, she is with me. A calm settle in my heart.

“My little one, everything will be fine. We must go to the hospital so they can examine you properly. We will make sure you get really healthy.”, my mother explains.  

I try to answer her, but the words do not come. I am tired and it hurts so hard and feels like I am burning, this cannot be my own body. Maybe it is not real? I must be dreaming. Inside me i shout out, Mom came and woke me up!

The men with the white coats carry me down to a car. It is large and grey. On its side, someone has painted a huge red cross. Mom is allowed to sit next to me and in her arms, she holds Pelle. She smiles at me. But the smile is not as it used to be, because tears are glistening in her eyes. 

When we stop, they take me out and roll me into a room where the walls are sparkling white. Mom comes up by my side. I see her take my hand, but I do not feel it.  “What’s going on? “ 

I must have dozed back to sleep; because once again, I was awakened by hearing voices all around me.

Strange figures stand around my bed. They are huge. They’re wearing white clothing and they are wearing masks in front of their noses and mouths. I feel them squeezing and pulling on my arms and legs.  “Now you have to be completely still”, says a stranger’s voice.  

I see a table being rolled in, and on it were a lot of strange things. In the middle of the shiny table is a large syringe. I know what it is, because my mother once took me to a nurse who gave me a shot with a syringe like this. It had hurt so much. I think, “Are they going to put that huge syringe in me? No, they cannot! “  

Somewhere inside me, the fear has overcome the fatigue of the fever. I am roaring! A powerful scream came out of me that I never thought I was capable of.   I see my mother’s tear-soaked face. Someone tells me that I must be quiet, that mother and father are not allowed to come in, that they must take a sample from my back.   No, I do not want to!

I feel hard hands take a firm grip of my body. They turn me over. All I hear are the screams coming out of me. Shouts filled with fear, anxiety, and despair.  It feels so weird when their hard hands grab me. It feels like someone is cutting stripes of my skin off with a knife. The white demons talk to each other, but I cannot bear to understand what is being said. 

Nobody talks to me.

Then silence surrounds me. The demons have disappeared. I see mother and father come to me. My Mom slowly strokes my cheek and caresses my hair. Her hand feels cool and smooth like cotton. Dad takes my hand. Why do I not feel that he holds me?

Mom hums soothingly the songs I love. Her voice sounds like silver bells. Anxiety settles in my stomach. My body aches, but my head can no longer feel. Sleep wraps me in its security.

I can feel tears running down my cheek. It feels like the tears are eating into my skin. I want to wipe them away, but no matter how much I try to speak to my arms, they do not obey. They lie there on the blanket like large heavy logs, completely without their own will.

This must be how it feels to be dead.

This is how it is to end up in exclusion, in loneliness. This is how it is to be deprived of everything you thought would be forever. The family, the mobility, the life.

The year is 1958. I am six years old and have contracted polio.

Reflections by the grown up Gunilla:

I was really scarred.  This experience  created fears, anxiety, problems in the future that for many long years, I could not connect to my isolation. But now I understand it has affected me tremendously.  

In retrospect,  can now see that my parents ended up in social exclusion for many years.  They, like me, lost their voices. My social exclusion became enormous. I was too small to understand that it was necessary to isolate me. The health care system of that time did not have the insight that one should talk to children, explain whats going on, and provide some form of security. My isolation created a lot of loneliness, and a lot of anxiety that I carried with me all my life.  It created a big problem with knowing myself, and finding my own identity . It was always others who had decided my identity for me.

At that time, the respect for doctors, and healthcare workers was so enormous. As a relative of a patient, you bent and bowed and never questioned a doctor’s or staff’s decision.  

I remember so well when the daily rounds were performed at the ward. There was always a tense atmosphere in the ward, nurses and assistants hurried back and forth to fix the bedding. They took away things that did not have to stand out. It would look neat so as not to annoy the doctors in any way.

When the rounds started, the doctor always came in first; wearing a clean white coat, a stethoscope hanging around his neck, and pencils in his breast pocket.  Those days only men served as Doctors.  They often came with their hands in their pockets followed by a bunch of candidates who idolized this powerful man, “the doctor”.  Then in came the nurses. The first nurse to arrive was the wards ‘responsible nurse’.  She carried a tabbed folder which she kept incredible control of at all times. It was our medical records, our test results, etc. As the team approached each patient, she would mumbled details from the chart about what had happened, what was going to happen, etc. They talked about us, not with us.

At most a doctor could say something like “here I see it better”, “how are you?”, but he never expected a response from the patients. The nurse took care of the answers by reading in the medical records about how the fever was, how the pain was, how the mood was. Careful instructions were then given by the doctor and then they swished out of the room.  You were not a person, you were just a sick child or a sick adult who had no voice.

For my parents, this period was an extremely difficult period. For some reason, my mother was especially ashamed that one of her children had polio. As an adult, I have met other people with polio who have the same experience. Something that currently feels very strange. But the spirit of that time was so incredibly different.

I remember that when I got home, in the evenings I could hear my parents talking low in the kitchen. They sometimes discussed how to deal with my physical problems. I do not really know what they decided, but something I noticed throughout my upbringing, and even in adulthood, was that people talked about my disease as “she got a flurry of polio”.  Then everything was good. Somehow that phrase would smooth over everything that happened and everything that came to happen. A denial of reality.

Maybe it was their way of dealing with the difficulty of polio. Because, of course, it was hard. There were many doctor visits, surgeries, orthotics had to be changed, physiotherapy, baths, and shoe adjustments. It took a lot of time.  I took a lot of time. And at the same time, ordinary life had to go on.

My older sister also ended up in the shadows. There was a 6 year age gap between us, so we were at completely different stages in life when I got polio.

What I remember clearly is that great demands were made on her to also be enormously good. She studied to be a nurse.  She was good at home and would always be my role model, according to our parents. She was often told that she was my role model, and I was often told that I would take after my sister. A responsibility that was certainly heavy to carry many times and these word created a lot of anger in me.  I was never allowed to be just me, I was never good enough. I had to live up to something I could not.

I certainly reacted and acted more negatively than I really should have.  But in me, my negativity was just a form of tremendous protest. I was already really scared and something in me just screamed ”NO” when more demands were made on me.

Kia ora koutou – may you all be well!

Kia ora koutou – may you all be well!

My name is Karen Butterworth. I’m a Kiwi – not a small brown fruit or large wingless bird, but a fawny-pink New Zealander (I hate the words ‘white’ or ‘black’ applied to people). I’m a 4th generation Kiwi of the Pakeha variety; that is, lacking any Maori descent. I am learning to be bicultural as a basis for welcoming all cultures to our shores.

In 1943, aged nine, I was paralysed by polio in all four limbs and trunk. I made a partial recovery, then led a ‘normal’ life by concealing my weaknesses wherever possible. In the mid-20th century this was prudent, otherwise you were treated with pity, contempt; or occasionally, admiration for your ability to do simple everyday things. E.g. ‘Karen just got up that step!’ There were exceptions. Some people just treated you as a human being.

In the 1990s, when the Late Effects of Polio made my disabilities more visible, I slowly became a proud polio survivor.  I joined the Post Polio Support Society of New Zealand (now PolioNZ), where I exchanged tips with others on living with our condition, including how to demand respect by standing proud (figuratively, because few of us could do so literally). My specialty was, and is, speaking proud. Thank goodness polio left my vocal chords intact! I also write proudly, today with the aid of a voice-operated system.

Some of you may be wondering what the Late Effects of Polio (LEOP) is. It is a progressive condition, that comes to many polio survivors 30 to 60 years after the initial disease. It can be slowed by prescribed exercising and pacing. The best explanation I have read is in ‘The Polio Paradox: What You Need to Know’ (2004) by Doctor Richard Bruno, who now has an informative Internet presence, see especially http://www.postpolioinfo.com/bruno.php  My posts on this site will focus on my life with LEOP over the past quarter-century.

Haere ra (Farewell)

Karen Butterworth