Hello
All,
Today
I am posting something written by one of our members. I have been having a very
difficult time with paralysis, weakness, “brain fog” and more the past week. I
posted this information on our PPN Support Group board a few days ago. I also apologized for not
responding to everyone’s posts like I usually do. Maureen wrote the following
in response and I wanted to share it with everyone. It is important for others
to know what it is like to live with Periodic Paralysis.
“With
much admiration and appreciation for your perseverance and dedication…You have
no need to apologize for anything. Wish that your conditions weren't robbing
you of vitality. It is hard enough to deal with physical incapacitation and
pain drain, let alone depletion from difficulty breathing and effort to sustain
let alone push through despite how you are feeling. To have brain fog adds so
much more depletion and challenge. It does get harder to get replenished.
Because of our physical compromise that results in slowness, lack of movement, and
even immobilization, we wouldn't think about correlating the effects of our
condition to compare to that of an athlete. And to people who don't have
conditions like PP (let alone having any additional disorders), it probably
seems ludicrous to use an athlete as an allegory to being a person with PP.
But
the extra exertion on our body to have to work in the condition of how we're
compromised and with so many obstacles in order to just be managing to sustain
basic function seems comparable to the effort that athletes exert to accomplish
their goals. But the efforts they need to exert, to achieve their goals are
self-imposed and voluntary choices. We aren't given the choice when our DNA
dictates what our bodies are going to have to deal with in order to function to
accomplish the goal of living let alone strive to accomplish projects and tasks
that give meaning and purpose and fulfillment.
Living
with a condition like PP requires more effort and endurance than someone would
have to do who does not have this kind of physical compromise. Living with PP
is like being an athlete, such as a marathon runner or a swimmer, because more
exertion is required for an athlete to reach a higher level of performance and
with PP our bodies have to perform at a higher level of exertion in order to
perform in the 'race of life'. But unlike being in a marathon, there aren’t
scheduled breaks to anticipate and provide opportunity to be refueled. No one
would expect a car to keep going without fuel or with electrical failure or
mechanical failure. And no one would expect a runner to run with mud closing in
around their feet up their legs or run barefooted through obstacles like glass
or sharp pebbles or unstable ground with rocks and holes that would hinder
their performance or could even be dangerous or a swimmer to swim in mud, clay
or quick sand.
With
PP that is what our bodies are dealing with in terms of having extra obstacles
and challenges to function. But unlike an athlete who can build up endurance
through pushing themselves physically, we get more depleted when we push
ourselves. We can't build up endurance when we put in more effort and we won't
experience the reward of expanding greater physical capacity, greater
well-being and health benefits that an athlete gets the benefits of through
their exertion. So it seems like PP is more challenging, physically, than the
challenges of being an athlete, with what appears to be less reward and
benefits. So, maybe it is ludicrous to correlate having the challenges of PP
with the challenges of being an athlete.”
Maureen,
Thank you so much for sharing with us. What a creative way to explain the challenges of living with Periodic Paralysis!!
Thank you so much for sharing with us. What a creative way to explain the challenges of living with Periodic Paralysis!!
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