Living with
chronic pain I was
diagnosed with FMS/MPS syndrome in 1996.
My
chronic pain started in 1990 after an auto accident. the doctors
kept saying it was nerve damage, but would heal. Although, my
injuries required several surgeries, I knew my pain was not
where the injuries were. I had never taken pain medication in my
life, except rare instances, when I had surgery, severe tooth
ache, or a severe injury. I seemed to have a high tolerance to pain, and would
take the medication a day or two, and the rest would sit in the medicine
cabinet. Once I was burned severely and although I
welcomed the pain reliever when I arrived at the emergency room, by the next
day, I was coping with the pain without taking any of the
medicine I had in a bottle on my bed side table. Now though, after
the 1990 accident, the pain seemed more severe each day. It was
a pain I could not tolerate. The
doctor at the bone and joint clinic would not give me any
medicine to relieve the pain, and I began to lose sleep as the
pain was so severe, sleep eluded me. It actually seemed worse in
the evenings and night. I would finally fall into exhausted
sleep as the sun was rising. I finally decided if this was nerve
damage and did not heal, I could not live my life with this
horrible pain. I would kill myself first. That pain lasted
several years without letting up. Then a new pain appeared
without warning. Doctors would say, you can't hurt in that
area. there is nothing there. I could draw the area where
the pain was. I finally decided I had a tumor and it was cancer
in the last stages as no one could hurt so bad and not be dying.
After eight months of constant pain it left in a split second as
I was walking across the room. How wonderful it felt to suddenly
be pain free is beyond description. I stood stock still, afraid
to move. I savored the wonderful feeling and just knew if I took
another step forward it would return. I must have stood in that
spot the longest time, and finally took a hesitant step, then
another, and another. the pain was gone. I wish I could say the
pain never returned, but it did come back, in another area of my
body. I have had days, weeks, and on occasions even a month of
being without unbearable pain. Never completely pain free, but
pain I learned to cope with. Finally a Rheumatologist
dx'ed me. Now my pain had a name. I looked it up on the internet
and joined a support group. I realized I was not alone dealing
with constant pain and doctors who were afraid to give
medication for fear of addiction. hey, doc, I already have an
unwanted addiction. one that will last my life time. unwanted
constant pain that has me in it's grip like a vise. I can not
work, enjoy my family or children as I dwell on my pain. Give me
relief from my pain, and let me live a normal life. I moved to
West Tennessee and behold found a doctor who was not afraid to
treat pain. Being pain free gave me a whole new life. I was even
able to go back to work, clean my home, cook, play with my
grandchildren, my great-grandchildren, and be a joy to my loved
ones. I guess all good things do end. One of our citizens had a
daughter on drugs and she had conned the doctor with a false illness
and her mother formed a group that had the gall to be named
GOD. the god's took picket signs and walked in front
of the doctors office. they called the drug task force, the FBI
and complained. Because he had treated so many for pain, he lost
his license. Hello pain, no I do not welcome you back. I again,
no longer work, my house work gets done when I can manage it.
Five of the doctors patients died within two months after he was
barred from his practice. I now fall asleep as daylight
is creeping in my windows. I may sleep a few hours and the pain
awakens me as it needs my attention. It has taken days to type
this article and I must again stop as the constant typing is
causing pain in my wrist, hands and arm. I may upload this and
finish it as pain permits. The only Rheumatologist that takes my
insurance is over a hundred miles away. I no longer drive, so I
just suffer like before.
Thoughts for today. Sept 27, 2005A
fair day so I will try to collect my thoughts and put them down.
We fibromites get so angry because doctors will not treat our
pain. I now realize why, since my doctor lost his license to practice,
because he was considered a "drug doctor" Dr. Ross and
his family moved into our small community and he set up his practice.
Once people learned he would treat pain, if the patient had
medical proof from a previous doctor, his office was full. No
other doctor in our county would prescribe pain medicine so
naturally "people came" His waiting room was filled
with suffering souls. Most had been traveling hundreds of miles
to pain clinics and to doctors in large cities. Some had
been seeking treatment out of state. A few like myself had been
suffering in silence. Dr. Ross thought he was covered since his
patients brought their medical records with them. He didn't have
to have a fancy lab, or a lot of nurses for treating pain and
writing prescriptions for high blood pressure, thyroid problems,
and other none narcotic medicines It was an easy way to make a
living. He cared about his patients. I took my book written by Devin J. Starlanyl ....
http://www.sover.net/~devstar/that
I used as my pain journal. He actually asked if he could borrow
it. I felt that finally at last I had a doctor who cared. I am
sure he was fooled many times by people who were not in pain,
but what doctor isn't unless they are ones who will Not treat
pain. What happened to him is the very reason other doctors are
"afraid" to give pain medication. The medical
profession wants people with chronic pain to go to pain clinics,
but they are only located in large cities. People with FMS find
traveling difficult if not impossible. driving over a hundred
miles to a pain clinic would put me in a flare that would last
for weeks or months. I made an appointment with a Rheumatologist
who I was told over the phone treated Fibromyalgia. It did not
take long for me to determine this was not true. As a new
patient I was given the standard form to fill out. The form
required only basic issues, how many surgeries, hospitals, illness',
had I had. allergies and basic questions. only one page. Not a
question that pertained to someone suffering chronic pain. Once
in the doctors inner chambers, I was sent for x-rays. Now anyone
who has FMS/MPS knows it does not show up on x-rays. When I
finally saw the doctor, as I sat on the examination table, he
took each arm in turn and raised it, pulled them back and then
ask me to push against his hand. That was it !!! I have had
every spot the FMS chart shows to be affected at one time or
another, I flatly refuse to have a pelvic exam as I would go
through the ceiling and then suffer horrible cramps, searing
burning pain for months afterwards. I have been single the past
fifteen years for that reason. Before I got Devin J. Starlanyl
book, I had let dentist pull perfectly good teeth because of dreadful
toothaches. I can not stand to be touched because it hurts. Even
a well meaning hug from grandchildren is painful. Yet this
doctor gently moved my arms and that was the extent of his
examination. Treat Fibromyalgia?? I think not. The only
prescription he gave me was for cymbila or something like that.
He said it was for pain. The instructions said it was an
antidepressant. The side effects were hostility, suicidal
thoughts, tremors, and the list went on with ghastly things. I
threw it in the trash. It
is a mystery to me why doctors will give people antidepressants
that have tragic side effects and keep people on them the rest
of their lives, yet refuse pain med as it is habit forming.
Duh!!
What
is Fibromyalgia.
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