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Post Polio
Syndrome
What is post-polio syndrome?
Post-polio syndrome (PPS) is a
condition that affects polio survivor’s years after recovery from an initial
acute attack of the poliomyelitis virus.
PPS is mainly characterized by new
weakening in muscles that were previously affected by the polio infection and
in muscles that seemingly were unaffected.
Symptoms include slowly
progressive muscle weakness, unaccustomed fatigue (both generalized and
muscular), and, at times, muscle atrophy. Pain from joint degeneration
and increasing skeletal deformities such as scoliosis are common. Some patients
experience only minor symptoms. While less common, others may develop visible
muscle atrophy, or wasting.
In the late spring of 2007 I received a call
from a lady inquiring about my
willingness to speak to her Post Polio Group. I explained to her that
though I was a nurse
as well as a hypnotherapist, I knew very little about polio
and even less about
post polio syndrome. She then explained to me, “that was the problem, very few
health care providers did.”
I told her that I would take to research PPS and
would speak to her group.
During my research I found all sorts of ways to deal
with the physical difficulties of PPS but not much further. Research told of
mechanical devices: lifts, braces, wheelchairs and other aids to maneuverability.
There were those who wrote of overcoming occupational difficulties and tools
and methods that might help those still working. There was much interest in
physical therapy and methods to preserve needed energy. However, the shear absence of other human
needs not mentioned, spoke
volumes to this researcher. It seemed the people that were providing
insight into this illness had totally forgotten that those suffering were more
then their bodies.
There was no mention of the mental devastation
that shattered ones life when polio reappeared. It appeared that no thought was
given to emotions:
depression, guilt, anger, embarrassment, frustration, fear,
sexual needs or spousal/family relationships.
I spoke to the Post Polio Group. I explained that
they were more then their
bodies and they were not their disease. That they
were far greater than that, and they could move beyond this if they absolutely
refused to let PPS define who they were. I then offered my assistance.
First and foremost we had to deal with the
debilitating pain that came with
post polio syndrome. It was not as if they
were a child dealing with polio,
for a child has little more to do but to
adjust to their limited abilities and most do so quite quickly. A surviving
adult however, has long forgotten those difficult days and are now functioning
pretty much as everyone else. They have families, children, careers, social
commitments and hobbies.
Then when least expecting, the polio returns.
When PPS begins to show symptoms in the person’s
life the first reaction is denial, “This can’t be happening to me.” Then the
long terrible process of diagnosis begins. Few doctors fully understand what is
happening to their
patient. Without a diagnosis, lengthy treatment is focused
on symptom solution.
Eventually, the patient is faced with the fact that their
polio has returned.
Confused and devastated, their life becomes full
of fears. What will happen to my job, where will the money come from, will my
spouse or children still want me? What about my friends, my hobbies, how will I
live and how will I get around. Then after all of these fears, thoughts and
heart aches have taken affect: where do I find help?
First it is to remember, we are not medical
doctors, physical therapist or occupational therapist; we deal with those
matters of the mind. The trained
Certified Hypnotherapist can be so very
beneficial to those suffering from PPS as our approach should be directed to
the whole person: body, mind
and spirit.
First the body:
For the body to function comfortably we must rid
the pain. For most chronic
pain cases, I stopped using traditionally
taught pain control techniques
quite some time ago. I now work in deeper states
of consciousness, negotiating with the unconscious mind to eliminate pain
levels that are no longer
needed as a symptom. With the help of the unconscious
mind any discomfort will only be available as a warning to the client, telling
them to take a
break, sit down, and relax, to restore and preserve energy.
Once the pain is brought under control, we can move
on to other issues. It’s important to understand that just because a client may
have PPS; it
does not exclude them from all the other difficulty that everyone
else has in life. The therapy I use from this point forward is Analytical
Hypnotherapy and Regression.
The mind:
It’s through acceptance we find peace.
Therefore, our main focus is on the
fear. As most fears are generated from a
remembrance in the past, the best
place to look for the cause of present fear is
in the past.
As past fears are remembered and/or relived,
they can be seen for what they really are, either real or perceived. As
forgiveness, acceptance and
resolution occur also comes a feeling of
empowerment. Each and every past
fear properly resolved will
exponentially increase the client’s empowerment.
With this empowerment we can now approach the
client’s new fears associated with PPS with their success from the past, after
all they already have dealt with previous fears and these new ones may appear
to be just another series of challenges of little or no consequence. This is
not to diminish these current and future difficulties. However, now it may seem
as not so overwhelming, nothing they can’t handle.
The spirit::
Most people have some sort of a concept about
life after death. Through the
counseling process the client must come to
understand that they are also, spiritual beings as well. That this life is a
temporary experience and
beyond it they live on in a spiritual existence.
At some point near the end of therapy, where we
really want to be with the
client, is to have the client say: “Okay, I have
PPS, so what. I had polio
as a kid and I have it now. I dealt with it then and
I can deal with it now. As
I look back on my life I can see how everything all
came together, how a power larger then I helped me through it and I don’t need
to be afraid anymore. I can now understand and accept that this is a temporary
lesson I needed to learn for my soul’s edification and I am blessed”.
A
client wrote the following article for a PPS journal.
Hypnotherapy - As an Alternative Therapy
By: Barbara Oniszczak
In all my reading about polio and post polio syndrome, I have
found and
continue to find articles regarding polio, what polio did to my body,
my physical ability, my physical disabilities, my limited mobility, my
inability to find
knowledgeable physicians, and medical professionals, my use
of orthotics, bracing, assistance devices, and the list could go on and on about
physically "fixing" my disabling condition(s).
There is a body/mind/spirit connection that is primarily
omitted in everything I read on a daily basis. In all the paperwork I have
collected over the
years from knowledgeable doctors, nothing in any of them had
addressed the
aspect of healing the body with mind and spirit forces that we
all possess from birth. This omission is included in newspapers, magazines,
journals and health articles as well. This body/mind/spirit connection is
convoluted but simple to address. It is an alternative therapy that needs your
attention. I have been fortunate enough to meet a Master Hypnotherapist
who has
guided me, and a few other survivors, on a journey that each and
everyone who
has a disabling condition must go on.
My primary purpose for
contacting Charles Kinney, Master Hypnotherapist
was as a speaker at my support
group meeting. Members had
expressed an interest in having someone come and
talk about that
body/mind/ spirit connection which we all have as human beings.
I'm not talking
about religion here, but the honest to goodness spirituality
and soundness of
mind, of which we are all made.
Mr. Kinney was eager to take on the challenge of learning
about post polio syndrome and would, if
he could, help me and others heal in body/mind/spirit on our PPS
journey. I needed to accept my post polio, and in accepting my inability to
function as I thought I should function as a 59 year old woman, I could relearn
and realign my thinking to be my source of strength, my source of
healing, and my source of energy. To conserve energy, I needed to accept my
body limits, what I can and cannot do; what I should and should
not do. So far,
I have been able to work on three main issues of my post polio journey. First, Mr.
Kinney and I addressed my chronic pain. I daily found myself functioning, or
rather trying to function at a level 9 of chronic pain. After my first session
of hypnotherapy, I found that I could reduce
my pain level to a 1. I did not
perceive my pain level to be a 1, but it is genuinely a 1.My pain level has
remained at a "one" since my therapy began. Next we worked on my
fears. I feared the uncertainty of my future and what it will bring. I feared
that I cannot be the wife and mother I once was.
I feared that I cannot
be as physically active on some days as others. I feared
what people say, think
or do when they learn about me slowly
returning to a disabling condition. After
all, I now wear two leg braces I've
never used before.
I know that I need to
address my physical limitations. I truly know what they
are and I know how to
control them. "Conserve to preserve" has real
meaning to me now. I
feel weakness. I feel the need to sit down when my legs say so. I am compelled
to do what I know I should do and I do so
because I know my energy is needed at
another time. I don't feel desperate in my need to DO things I believe are
expected of me. I have a stillness about me that is more important than what I
thought needed to be done now. Instead of being on a collision course with my
PPS, I am now working
body/mind and spirit in living with my PPS. I am not on
the downward spiral that I once was on. I was on that downward spiral a few months
ago. Ask the other members of my support group and they will echo what I have
said: body, mind and spirit are all connected. You are what you think
and you are
what you believe. My body knows this, without a doubt.
Barbara Oniszczak,
Facilitator, Northeast MI Support Group
Polio Perspectives Vol 22 No 3 Fall 2007 16
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