Video
Transcription by
Denise R. Alberigi
Mother of Amanda
Dedicated parent to finding a cure
HOW
TO HELP
Juleen
Stramiello
Cofounder and Past President
JULEEN STRAMIELLO:
Hello, my name is Juleen Stramiello and this video
has been produced to promote the need for research
into a disease called reflex sympathetic dystrophy
also known as complex regional pain syndrome.
Reflex sympathetic dystrophy, commonly called RSD,
is a debilitating, chronic neurological disease
caused by a malfunction of the sympathetic nervous
system which can cause excruciating pain. Throughout
this video you will see clips from television broadcasts
concerning RSD patients.
Have you ever heard of Reflex Sympathetic Dystrophy?
ABC NEWS REPORTER #1:
So, Marti, have you heard of RSD?
ABC NEWS REPORTER #2:
I have never heard of it before.
ABC
NEWS REPORTER:
"Most people have not heard of RSD"
ABC NEWS REPORTER #1:
Well, most people have not.
CNN NEWS REPORTER:
2 ½ to 3 million Americans suffer constant pain
from a disease you have probably never heard of.
CBS NEWS REPORTER #1:
Reporter Mary Beth Byrd joins us now to tell us
about what's called RSD.
CBS NEWS REPORTER #2:
That is right, those are the initials.
CBS NEWS REPORTER #3:
Never heard of this.
CBS NEWS REPORTER #2:
You are not alone. So many people have not, and
that is the problem with RSD. The full name for
this condition is reflex sympathetic dystrophy and
you really don't hear to much about it, and that's
why so many people don't recognize the signs when
they get it.
JULEEN STRAMIELLO:
You see, so few people have heard of RSD. Usually
only the patients who suffer from it, and the doctors
who treat them. So, what exactly is RSD?
DR. ANTHONY KIRKPATRICK:
We don't understand why that is. We think it has
to do with a reflex. There's a reflex that is going
on and on and on, we have to go in there and block
it temporarily and it just can't get started and
wound up.
JULEEN STRAMIELLO:
As you can see, RSD is quite complex and its causes
are not known. We here at the foundation are dedicated
to finding what causes RSD and finding a cure for
this dreadful disease. So, what does it feel like
to be afflicted with RSD?
CNN NEWS REPORTER:
A knee injury triggered her bout with RSDS 18 months
ago.
Sarah
Young
SARAH YOUNG:
I don't like what happened to me. I don't want it
to happen to me anymore. I want to be a normal teenager.
SARAH'S MOTHER:
It took awhile to show up what it was, after going
to multiple doctors who did not...they were clueless.
I had a couple of doctors tell me to cut her leg
off. Her leg would be so blue and ice cold.
Justin
Raulerson
CNN NEWS REPORTER:
Justin Raulerson is 14 years old and is now back
in a wheelchair because the pain is so intense in
his lower right leg. Justin's mom Renee says it
began with a broken ankle 2 ½ years ago. Even after
the cast was put on the pain only intensified.
JUSTIN'S MOTHER:
The doctors kept telling me every night, it's in
his head, it's the kid. I would say no it is not.
There is something going there!
KATHLEEN STEWART:
You will have different people who have RSD describe
it in different ways, but one of the universal descriptions
is the burning pain, the part that is affected is
on fire.
MELISSA LISCOM:
You know how when you hold an ice cube and you hold
it in your hand for too long and it starts to burn
but it's cold, that's kind of what it felt like.
BETH McDONALD:
The burning just became outrageous. Just a burning
like if you have a fireplace at home and you put
your hand in it, it feels like that, that is how
I lived every day.
JULEEN STRAMIELLO:
Some healthcare professionals are either unaware
of RSD or do not know how to diagnose it. Many cannot
understand what is wrong with the patient and cannot
offer them any assistance. It is not rare for an
RSD patient to go to several doctors before they
are finally, correctly, diagnosed with RSD. It is
actually a relief to patients just knowing what
they are experiencing is not just in their heads
but is a real and a very serious disease.
CBS NEWS REPORTER:
For Kathleen Stewart being diagnosed with a terribly
debilitating disease was actually a relief. The
pain started with an infection in her arm and from
there it spread. It took six months for doctors
to diagnose her with reflex sympathetic dystrophy
or RSD. It is a disease of the nervous system that
can result from a simple injury like a sprain. The
pain it causes can be unbearable.
Dr.
Anthony Kirkpatrick:
"Unfortunately, there is no specific
laboratory test for this disease."
DR. ANTHONY KIRKPATRICK:
Unfortunately, there is no specific laboratory test
for the disease. You have to rely on your clinical
skills. You have to be looking for objective findings
in the patient.
JULEEN STRAMIELLO:
University of South Florida professor Dr. Anthony
Kirkpatrick explains that early diagnoses is vital,
that at times, it is extremely difficult because
of lack of awareness in physicians. Also, there
is no single diagnostic tool that can identify RSD.
Clinical knowledge and experience along with a detailed
case history and examination is necessary for arriving
at an early diagnosis. RSD along with other causes
of chronic pain can lead to forms of emotional suffering
such as depression, anxiety irritability and even
suicide. In children the loss of pleasurable activities
and a sense of helplessness only adds to their pain.
In February 2002, I attended an International Symposium
on RSD. The number of individuals from around the
world that suffer from this disease astounded me.
There were people in full bed cots with blankets
covering their affected areas. There were children
in wheelchairs in pain with their parents sitting
beside them feeling hopelessness and despair. There
were both adults and children using canes, crutches
and walkers grimacing with each step. I noticed
some patients crying. Some of these individuals
have lost an extremity due to RSD. Not because of
the pain, but because of complications of this disease
such as recurring infections.
CBS NEWS REPORTER:
For Beth MacDonald her experience goes back 11 years.
It has spread now throughout most of her body and
has already taken one of her legs.
Beth
McDonald:
"My leg was going to
become gangrene."
BETH McDONALD:
I asked them to take my leg off because I just couldn't
... the pain was so bad beneath my knee and I couldn't
clean it out. It was going to become gangrene and
blood disease and everything else.
JULEEN STRAMIELLO:
As I watched these courageous souls at the recent
symposium, I realized how fortunate I am that I
have responded favorably to sympathetic nerve blocks...
Oh, did I forget to mention that I too am afflicted
with RSD. Just a few years ago I was nearly bedridden
and wheelchair bound. This disease is devastating
and a cure must be found for the millions of people
who suffer from RSD around the world. The International
Research Foundation is committed to the establishment
of a world-wide network of research centers creating
a database with up-to-the-minute results on ongoing
RSD research. The Foundation is committed to raising
funds to support clinical investigations anywhere
in the world that show a promise of curing this
dreadful disease. We cannot accomplish this on our
own. We need your help. Your donations for help
support the critical research necessary to cure
RSD.
To find out more on how you can help us, please
visit our website at WWW.RSDFOUNDATION.ORG,
or call our International Headquarters in the United
States at 1-813-907-2312.