"People May Not Remember Exactly What You Did, or What You Said, But They Will Always Remember How You Made Them Feel"
-Unknown
I've been told quite a few times in my life that curiously, I have a "way" of explaining things that sorta makes whatever I'm talking about, not only understandable, but almost...palpable. (Wow - Kudos to ME, right?! : )
What's my secret? - I like to talk in metaphors...that's it! (Um...Sorry to disappoint...) But it's actually the only tool I have that enables me to "bridge the gap," between what I may experience that you may not understand. How do metaphors help with this? Well...it gives me the opportunity to allow you to momentarily "feel" (using symbolic analogies) what I feel. Actually, it's pretty easy...
I often get a LOT of questions from various people, asking me to describe my symptoms...most times they are surprised at what I end up saying (which I find extremely entertaining : ) So - here's the list:
Note: Thankfully, I do not feel like this ALL of the time, and I certainly cannot say that other Lyme suffers have the same experiences I do, but I CAN say that throughout my long history with this illness, every single one of these "metaphors" have been fully felt and expressed in the exact manner I describe below.
Note: Thankfully, I do not feel like this ALL of the time, and I certainly cannot say that other Lyme suffers have the same experiences I do, but I CAN say that throughout my long history with this illness, every single one of these "metaphors" have been fully felt and expressed in the exact manner I describe below.
1) Q. What does having Lyme feel like?
A. It feels like I'm trapped in prison with a really annoying,
life long neighbor. One who simply refuses to leave me
alone...REFUSES!!
of those "Get OUT of Jail Free" Cards! Sigh...this whole set-up we got going here, is seriously driving me BAT-SHIT crazy!!
*Notice how I'm "personifying" a bacterial infection here. This is not a mistake - every single Lyme patient I've ever met will tell you the same thing. They very strangely, and quite uncommonly feel as though they're playing a torturous game of ME vs. IT. They are oddly aware of its presence...which is something I've NEVER felt about any other type of illness or infection I've ever had.
2) Q. What do you mean when you say you feel
weak and tired?
A. Are you a swimmer? When you were a kid, did you ever
have contests with your friends to see how long you could
hold your breath underwater? If so, do you recall the
sensation you felt, just a
millisecond before you
decided you couldn't take
it anymore, and came up
gasping for air?
Remember how the "life"
seemed to drain out of you,
and you felt your entire
body almost go limp as
you started to fade out (right
before you came up for air)?
That momentary sensation you felt, the one that made you
feel like you were going to die if you didn't get oxygen...Yeah
- that's how "weak and tired" I feel every single second on
most days.
3) Q. What does the "pain" in your spine, joints,
and head feel like? Didn't the IV Rocephin
help with that?
A. Have you ever cut your finger, or some other body part, that
eventually became infected? Do you recall what it felt like?
It's an unmistakable burning, tingling, gnawing, infection-
type pain. Now, remember when you came to your senses and
FINALLY put some Neo-sporin, hydrogen peroxide, or some
other topical antibiotic remedy on the infected area?
Notice how doing so seemed to tame that "fire" you felt?
How you kind of sighed with relief, knowing that doing so
was exactly what your body needed to fix the problem? It was
soothing and comforting, right? The area surrounding my
spine, joints, and head feel very much like that "infected
cut", and for the first few months, receiving the IV Rocephin,
felt almost like a liquid Neo-sporin. It had a way of "taming
that infectious fire" and it allowed me to pretty much get on
with my day. Unfortunately, for me, the last few months were
different. I suddenly felt like I had a MUCH bigger "cut" and
was still adding the same amount of that liquid Neo-sporin. It
just wasn't enough anymore, and I slowly felt that fire come
back. It was only then that I just knew I was in serious
trouble...especially when my Dr. suddenly decided it was
time to STOP the treatment, but that's a different story.
4) Q. What are your thoughts about applying for
and receiving disability for Lyme Disease?
A. I find that the "disability" process is quite similar to
suddenly waking up one day and realizing that your house
and everything you own is on fire. Frantically, you start
calling the fire department, the police, and every other local
entity that may assist you, while barely managing to crawl
to safety without becoming engulfed by the flames yourself.
You mistakenly think that the people you called are on their
way, but it is only after EVERYTHING you ever had is lying
in molten ash around you, and you are left with nothing, that
they finally decide to show up.
*The rest of the following questions, I actually don't have metaphors for, BUT I am happy to answer them all the same : )
5) Q. If you're SO disabled, how can you possibly
be writing a BLOG??
most days.
3) Q. What does the "pain" in your spine, joints,
and head feel like? Didn't the IV Rocephin
help with that?
A. Have you ever cut your finger, or some other body part, that
eventually became infected? Do you recall what it felt like?
It's an unmistakable burning, tingling, gnawing, infection-
type pain. Now, remember when you came to your senses and
FINALLY put some Neo-sporin, hydrogen peroxide, or some
other topical antibiotic remedy on the infected area?
Notice how doing so seemed to tame that "fire" you felt?
How you kind of sighed with relief, knowing that doing so
was exactly what your body needed to fix the problem? It was
soothing and comforting, right? The area surrounding my
spine, joints, and head feel very much like that "infected
cut", and for the first few months, receiving the IV Rocephin,
felt almost like a liquid Neo-sporin. It had a way of "taming
that infectious fire" and it allowed me to pretty much get on
with my day. Unfortunately, for me, the last few months were
different. I suddenly felt like I had a MUCH bigger "cut" and
was still adding the same amount of that liquid Neo-sporin. It
just wasn't enough anymore, and I slowly felt that fire come
back. It was only then that I just knew I was in serious
trouble...especially when my Dr. suddenly decided it was
time to STOP the treatment, but that's a different story.
4) Q. What are your thoughts about applying for
and receiving disability for Lyme Disease?
A. I find that the "disability" process is quite similar to
suddenly waking up one day and realizing that your house
and everything you own is on fire. Frantically, you start
calling the fire department, the police, and every other local
entity that may assist you, while barely managing to crawl
to safety without becoming engulfed by the flames yourself.
You mistakenly think that the people you called are on their
way, but it is only after EVERYTHING you ever had is lying
in molten ash around you, and you are left with nothing, that
they finally decide to show up.
*The rest of the following questions, I actually don't have metaphors for, BUT I am happy to answer them all the same : )
5) Q. If you're SO disabled, how can you possibly
be writing a BLOG??
A. To be honest, it took me about 4 years to be able to start
"writing" again. Even now though, my symptoms wax and
wane in such a way that there are times (a LOT of them)
where I look at what I've written so far and wonder how on
earth I was able to not only write an entire post, but even be
able to coherently organize, plan, and execute a single
fucking sentence! (As you can see this obviously frustrates
me...) What do I do to get around it? I write when and what I can, and try and be grateful that I'm able to do so...at least part of the month.
6) Q. Why are you constantly saying "I'm Sorry"
whenever you have those seizure-like
episodes, walking issues, and periods of
paralysis?
A. For the LIFE of me, I simply do not understand why people
don't "get" this! To me, going through this type of experience
while someone is watching is the most mortifying, horrifying,
and utterly embarrassing thing that could EVER happen!
I HATE it when people see me lose control over my body like
that! I mean - how humiliated would YOU feel if you
suddenly, for no reason at all, lost control of your bowels,
and actually shit
your pants in front
of everybody!
Thankfully that
humiliation has
NOT happened to
me, but I would
imagine the feeling
being quite similar.
I'm only 30 for
Christ's sake. SO -
let me say it again:
7) Q. You're going through so much...why don't
you ever cry?
A. For two very easy reasons. The first is that the saying,
"People can get used to pretty much anything" is very true.
In that respect, I've simply gotten SO used to constantly being
in pain, dealing with the financial hardships, coping with the
endless (self-inflicted) loneliness, and trying to just "get by",
that THIS reality has become almost "normal" to me. In fact,
the only time I actually cry is from any kind of RELIEF (Ha -
it's more like a "reprieve"!) I experience over any one of the
above mentioned being even temporarily abated. The second
reason is that (especially with the neurological, cognitive,
and psychiatric aspects of this illness) some of the symptoms
I experience are SO downright bizarre, incomprehensible
and astonishingly unimaginable, that when I experience them,
I often find myself in a state of complete shock and can not
even begin to mentally process such a phenomenon - much less
have an "emotional response" to it!
8) Q. Why does having "moments of clarity"
ultimately make you sad?
A. There are moments, even hours that randomly occur where
a shift takes place, and you suddenly, and without effort,
feel and perceive everything normally again. (You'll know
when this happens because you'll suddenly start wondering
with alarm, why on earth you AREN'T working, are living
with your parent's, DO NOT have a social life anymore, and
are SHOCKED to realize that you are NOW 30 years old! -
where did those three years go?!) While you experience this
you think it will stay, that you are "back" to your old self again, and you begin to have HOPE. Without fail, however, these moments or hours never last, and you can almost feel yourself being pulled back into "Lymeland". You desperately try to fight it, to hold on to this sudden clarity, but attempting to do so is pointless - it's like trying to catch the wind, and you watch helplessly as this feeling fades, as it slips right through your fingers.
*If you are reading this paragraph and managed to make it through to the end of this post - I sincerely Thank You! (I KNOW no one likes to hear about this type of stuff...usually, and quite understandably, it's simply easier to look the other way.)
However, please know that I am not looking for "sympathy" here, my intention is really to help people UNDERSTAND how life-changing this disease can be if NOT caught in its early stages, and one of the ways I can get that through to you is, unfortunately, by trying to have you imagine yourself experiencing the kind of insanity that comes along with the later stages of the illness.
Hopefully, by now, Lyme Disease is AT LEAST on your radar...it IS epidemic nowadays, and prevention and early treatment is KEY.
Best Wishes,
Sarah
"writing" again. Even now though, my symptoms wax and
wane in such a way that there are times (a LOT of them)
where I look at what I've written so far and wonder how on
earth I was able to not only write an entire post, but even be
able to coherently organize, plan, and execute a single
me...) What do I do to get around it? I write when and what I can, and try and be grateful that I'm able to do so...at least part of the month.
6) Q. Why are you constantly saying "I'm Sorry"
whenever you have those seizure-like
episodes, walking issues, and periods of
paralysis?
A. For the LIFE of me, I simply do not understand why people
don't "get" this! To me, going through this type of experience
while someone is watching is the most mortifying, horrifying,
and utterly embarrassing thing that could EVER happen!
I HATE it when people see me lose control over my body like
that! I mean - how humiliated would YOU feel if you
suddenly, for no reason at all, lost control of your bowels,
and actually shit your pants in front
of everybody!
Thankfully that
humiliation has
NOT happened to
me, but I would
imagine the feeling
being quite similar.
I'm only 30 for
Christ's sake. SO -
let me say it again:
7) Q. You're going through so much...why don't
you ever cry?
A. For two very easy reasons. The first is that the saying,
"People can get used to pretty much anything" is very true.
In that respect, I've simply gotten SO used to constantly being
in pain, dealing with the financial hardships, coping with the
endless (self-inflicted) loneliness, and trying to just "get by",
that THIS reality has become almost "normal" to me. In fact,
the only time I actually cry is from any kind of RELIEF (Ha -
it's more like a "reprieve"!) I experience over any one of the
above mentioned being even temporarily abated. The second
reason is that (especially with the neurological, cognitive,
and psychiatric aspects of this illness) some of the symptoms
I experience are SO downright bizarre, incomprehensible
and astonishingly unimaginable, that when I experience them,
I often find myself in a state of complete shock and can not
even begin to mentally process such a phenomenon - much less
have an "emotional response" to it!
8) Q. Why does having "moments of clarity"
ultimately make you sad?
A. There are moments, even hours that randomly occur where
a shift takes place, and you suddenly, and without effort,
feel and perceive everything normally again. (You'll know
when this happens because you'll suddenly start wondering
with alarm, why on earth you AREN'T working, are living
with your parent's, DO NOT have a social life anymore, and
are SHOCKED to realize that you are NOW 30 years old! -
where did those three years go?!) While you experience this
you think it will stay, that you are "back" to your old self again, and you begin to have HOPE. Without fail, however, these moments or hours never last, and you can almost feel yourself being pulled back into "Lymeland". You desperately try to fight it, to hold on to this sudden clarity, but attempting to do so is pointless - it's like trying to catch the wind, and you watch helplessly as this feeling fades, as it slips right through your fingers. *If you are reading this paragraph and managed to make it through to the end of this post - I sincerely Thank You! (I KNOW no one likes to hear about this type of stuff...usually, and quite understandably, it's simply easier to look the other way.)
However, please know that I am not looking for "sympathy" here, my intention is really to help people UNDERSTAND how life-changing this disease can be if NOT caught in its early stages, and one of the ways I can get that through to you is, unfortunately, by trying to have you imagine yourself experiencing the kind of insanity that comes along with the later stages of the illness.
Hopefully, by now, Lyme Disease is AT LEAST on your radar...it IS epidemic nowadays, and prevention and early treatment is KEY.
Best Wishes,
Sarah
