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This
is
my
story
of
PAIN
and
Much
More.
The
BEST
way
I
can
describe
this
pain
is:
Several
KNIVES
inside
my
lower
abdomen/stomach,
cutting
and
poking
from
the
inside;
then,
the
BURNING
~
All
this
lasts
for
the
entire
day
and
night
-
began
July,
2008
-
Still
Here.
I
have
been
in
horrific
pain,
my
stomach,
lower
abdomen,
24/7
since
July,
2008.
My
husband
and
I
have
been
to
every
doctor
possible
to
find
out
exactly
"WHERE
My
Pain
Is
Coming
From."
We've
seen
at
least
40
doctors,
counting
_several
trips
to
the
emergency
room,
mainly
because
I
did
not
have
a
family
doctor
whom
I
could
see
and/or
depend
on.
(See
"And
They
Call
Themselves
Doctors")
This
pain
is
like
trying
to
explain
to
someone
who's
never
had
a
"Headache,
Or
"Cut,"
just
what
it's
painfully
like.
I
was
diagnosed
with
Lung
Cancer,
September,
2007.
My
main
treatment
to
kill
the
cancer
was
"Radiation."
Thank
God
that
the
Treatments
worked,
but,
they
fried
my
Esophagus
along
with
other
problems
which
I'll
be
addressing.
So,
I
began
having
terrible
pains
in
my
lower
stomach.
Each
time
I
saw
a
new
doctor,
he/she
couldn't
give
me
a
reason
for
this
pain?
They
just
brushed
me
off,
said
to
go
home,
and
it
would
go
away.
The
pain
began
getting
worse
with
each
passing
day,
week
and
month,
until
it
was
SO
bad
that
I
was
debilitated;
only
able
to
"lie
down
on
my
sofa."
I
had
No
LIFE
anymore.
I've
always
been
a
very
active
person.
Walking
all
of
the
time
around
our
neighborhood
for
exercise,
and
jumping
into
my
car
to
go
to
various
places.
My
husband
and
I
would
also
go
out
to
dinner
several
times
a
week
with
our
friends.
I
had
a
life-style
of
just
being
active!
I
had
lost
so
much
weight
during
my
treatments,
that
it
also
weakened
me.
But,
when
I
received
the
first
"All
Clear
of
Cancer
News,
back
on
January
29th,
2008,
I
was
of
course
relieved
and
Thrilled!"
I
was
ready
to
resume
my
life
as
I
knew
it
before
the
Cancer
treatments.
After
a
while,
my
husband
made
an
appointment
with
a
Pain
Doctor.
At
first,
I
was
against
this.
However,
upon
my
initial
visit,
he
evaluated
me,
and
put
me
on
a
Pain
Medicine
called
Neurontin,
in
addition
to
Vicodin.
I
have
NEVER
liked
taking
any
pain
medicines,
or,
any
pills
either.
However,
at
the
point
I
was
at,
I
desperately
needed
pain
medicines
to
help
with
my
pain.
The
First
Pain
Doctor
did
not
work
out
at
all.
He
was
completely
unprofessional,
insulting,
uncaring
and
we
had
enough.
I
only
found
my
current
Pain
Doctor,
who I will be leaving Unfortunately After I had
surgeries with this man whom I've found to be inept, along with his Surgery for
ME: The placement of the Battery Pack and Wires/Leads attached to the back
of my head. I am having SO much pain from the back of my head, and chest
where the battery pack/stim is located. Next Step: Find a Qualified
Surgeon to remove all of this. I do NOT want to go back to the so-called
Pain Doctor who did this surgery, I just don't like or trust him. My body
is most likely 'rejecting,' all that's been surgically implanted; I've been
feeling "Sick," but not the traditional sick - a different sick,
and I'm Cold from the inside out, in addition to night sweats?
(See:
"My
Story")
We Found
another "Qualified M.D. Pain Doctor." I guess they say
"Three is the Charm? Let's hope so! He could NOT understand WHY
the procedure was placed in my chest, and NOT in my stomach where the pain is
coming from? This makes sense to me! I'm gong ahead with this
Doctor, a REAL doctor who'll listen, and will take phone calls from _his
patients, something Dr.T. never did nor believed in. Unfortunately, I fell
for his tactics, and should've listened to our Insurance Company when they
DENIED him, or the surgery he wanted to perform. He is NOT recognized with
the surgery I have. But, I was so desperate to get out of pain, that I
fought my husband, who ended up paying for my surgeries out of pocket. This 3rd. Pain
Doctor, wants to give me the Trial; placed in my stomach,
"Internal/Outer stomach
walls," to see if that works and kills the pain. If it does, we go ahead
with the permanent Surgery where the battery will be located somewhere in my
lower abdomen which makes MORE sense and attacks the PAIN at the
Source!!!! God, I pray so! The Trial will only be for 7 days instead
of 3 weeks as the 2nd. so-called Pain Doctor insisted on.
I can only hope and Pray very hard that this new
procedure will work for me; I can't take this pain much longer, and that's the
God's honest truth!
(Backing Up A Bit):
At
my
very
first
visit
to
Dr.
T,
I
had
the
fastest
exam?
He
asked
but
a
few
questions,
then
said
"You
Have
Permanent
Nerve
Damage."
Yes,
the
worst
kind
of
pain
ever.
In
his
opinion,
my
pain/nerve
damage
was
caused
by
the
result
of
the
Radiation/Chemo
treatments.
He
gave
us
2
choice:
To
be
on
pain
meds
for
the
rest
of
my
life;
or,
to
have
the
Neurostimulation.
Occipital
Stimulator
Electrode
Placement
(I
Had
4
Surgeries:
Trial;
Removal
Of
Trial;
Permanent
Stim;
Replacement
Of
TOO
Large
Battery
In
My
Chest)
I
had
the
aforementioned
procedure
done
April
15th,
2009.
I
wore the
Trial,
with
attached
electrodes
surgically
inserted
into
the
back
of
my
head/brain;
with
lead
wires
attached
to
an
external
battery/program
pack.
Permanent
Surgery July 21, 2009.
NOW
I understand why his procedure was denied! It is not
recognized by the AMA or the Insurance Company. After
all I've been through, with it NOT working, pain coming from
the back of my head, and in my chest where the battery pack
is, I can fully understand WHY it's been denied. This
procedure is Dr. T.'s Baby, he invented this
procedure. Had I had the conventional Stim
procedure: Whereas they place the leads down your
spine, with the battery pack somewhere down yonder, I
believe I would be Pain Free today! But, I got sold
down the river, and listened to that inept Dr. T. I stand
accused of being Desperate. Wanting a LIFE sans
any/all Pain. My mistake, and now I have to live with
it until I can find a reputable Surgeon to Remove what Dr.
T. surgically implanted.
   
PLEASE
READ
BELOW:
Addendum:
I
DO
understand WHY
our insurance company disallowed my surgery: It is NOT
recognized by them or the FDA. This is a procedure
that Dr. T. invented. I am living proof that this type
of Stim doesn't work! I am SO sorry we fought them,
and didn't try for another Pain Doctor - Qualified who's
done many procedures via the stomach, back, etc.
MAJOR
MISTAKE
~
FORESIGHT
I
had
my
surgery
for
the
"Occipital
Stimulator
Electrode
Placement
-
Permanent."
NEW
DEVELOPMENTS:
SOLD
DOWN
THE
RIVER
WITHOUT
A
PADDLE!
   
I
had
my
Surgery
on
July
21st,
2009
I
thought
that
right
after
the
surgery,
I'd
be
completely
Pain-Free
-
as
No
ONE
explained
otherwise?
No
one
ever
explained
the
complete
"Story,
Process
To
Me."
I
feel
that
since
I
was/am
the
one
suffering,
and
going
through
the
surgery,
that
they'd
at
least
explain
everything?
Well,
now
I'm
still
in
pain.
Would
you
believe
that
his
policy
is
that
"He
Will
NOT
Speak
With
His
Patients
Over
the
Telephone,
nor
Will
He
Return
Phone
Calls?"
I
cannot
believe
this?!
Please
tell
me
I'm
not
going
nuts!
I've
NEVER
had
any
doctor
who
wouldn't
call
back
their
patients,
especially
a
Pain
Doctor?
I
am
NOT
pain
free,
and
must
see
the
Neuro
Programmers
every
3
weeks
until
the
Pain
is
gone
-
If
Ever?
I
refuse
to
see
them,
and
I
am
going
to
a
NEW
Pain
Doctor
now.
Thus,
I
will
no
longer
need/want
Dr.T.
I
will
be
having
my
neuro
stim
=
back
of
my
head,
leads/wires
running
down
the
side
of
my
neck,
connecting
to
the
battery
in
my
chest
-
Removed
a.s.a.p.
I
do
not
know
if
I
will
have
the
Surgeon
who
did
this
surgery
remove
it;
I
think I would feel much more comfortable having another Surgeon remove what I
have, if I can find one that is.

About
My
New
Pain
Doctor:
Main
Site:
http://www.ct-neurosurg.com/index.htm
http://www.ct-neurosurg.com/ourdoctors.htm
Dr.
David Glassman
Dr.
Glassman
is
a
graduate
of
the
Sackler
School
of
Medicine,
New
York,
NY-Tel
Aviv,
Israel.
He
did
his
residency
training
at
Yale
University,
Department
of
Anesthesiology
as
well
as
a
Pain
Management
Fellowship.
He
is
a
licensed
M.D.
in
Connecticut,
New
York,
and
New
Jersey.
Dr.
Glassman
is
Board
Certified
by
the
American
Board
of
Anesthesiologists.
Dr.
Glassman
is
a
specialist
in
Pain
Management.

About
The
Practice:
|
Connecticut Neurosurgery, PC began as Neurosurgical Associates of New Haven in 1971 with Dr. Lycurgus Davey, Dr. Alvin Greenberg, Dr Franklin Robinson and Dr. Isaac Goodrich. Connecticut Neurosurgery has evolved into an integrated multi-specialty neuroscience center presenting a full spectrum of care across the continuum of adult neurosurgery, physical rehabilitation and medicine and pain management. It now consists of seven physicians including five operating Neurosurgeons: Drs. Thomas J. Arkins, Gary M. Bloomgarden, Isaac Goodrich, James K. Sabshin and Patrick Tomak, Pain Management: Dr. David Glassman and Physician Medicine and Rehabilitation: Dr. Martin Hasenfeld.
Our practice provides excellence in neurosurgical care. We offer responsive, caring service; state-of-the-art technical innovations; and many years of in-depth experience. All the members of our Group have achieved considerable expertise in specific subspecialties within neurosurgery, which include cerebrovascular; neuro-oncology; stereotactic;trauma care; and spinal services.
Above all, the emphasis of our practice continues to be patient-focused: consistently providing caring, competent clinical neurosurgery. Committed to continued advanced medical education, our physicians stay current in technical advances in medicine and neurosurgery, so we can deliver the most advanced care to our patients.
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I'll
Keep
You
Posted
-
Informed!
Wish
Me
Luck,
I'll
Need
It!
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