[Extensions of Remarks]
[Page E1706]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
NATIONAL DYSTONIA AWARENESS WEEK SEPTEMBER 28 TO OCTOBER 5
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HON. RON LEWIS
of kentucky
in the house of representatives
Wednesday, September 25, 1996
Mr. LEWIS of Kentucky. Mr. Speaker, I rise to inform my colleagues
about National Dystonia Awareness Week, September 28 to October 5,
1996.
I was privileged, Mr. Speaker, to attend a chili supper in June given
by a group of residents of the Second District who deal with dystonia
everyday. These residents regularly meet and discuss the challenges
they meet everyday.
Dystonia is a relatively rare neurological disorder characterized by
severe muscle contractions and sustained postures that afflicts an
estimated 300,000 people in North America. Dystonia is a complex
disorder that consist of three types and is often times misunderstood
and misdiagnosed.
The three types of dystonia are primary, focal dystonias, and
secondary dystonia.
Primary dystonia or idiopathic torsion dystonia [ITD], causes spasms
that affect many different parts of the body and often starts in
childhood.
Focal dystonias affects one specific part of the body and is
distinguished for five varieties. Blespharasposm causes eyelids to clse
tightly for seconds to hours. Cervical dystonia is the contraction on
neck muscles turning the head to one side or pulling it forward or
backward. Oromandibular dystonia--Meige's Syndrome--is a combination of
blepharospasm and oromandibular dystonia in which the muscles of the
lower face pull or contract irregularly to cause facial distortions.
Spasmodic dysphonia affects the speech muscles of the throat, causing
strained, forced, or breathy speech. Writer's cramp is characterized by
muscles in the hand and forearm contracting.
The last type of dystonia, secondary dystonia, is caused by an injury
or other brain illness.
Unfortunately, there is no known cause or cure for dystonia.
Researchers, however, have made promising advancements in
understanding this disorder. In 1989, Drs. Xandra Breakefield and James
Gusella made the discovery of a genetic marker that will significantly
advance future research. In addition, hundreds of dystonia patients and
their families have made the commitment to donate their brains to
further dystonia research.
Mr. Speaker, I would like to thank you for allowing me this
opportunity to familiarize my colleagues with dystonia and encourage
each of my colleagues to learn more about this neurological disorder.
More information about dystonia can be found on the world wide web.
The Dystonia Medical Research Foundation's home page not only offers
information about dystonia, but also details meeting places and dates
for those who are or have a family member affected by dystonia and can
be reached at hhtp://www.iii.net/biz/dystonia/. You can also learn more
by visiting an internet newsgroup dedicated to dystonia at
``alt.support.dystonia.''
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