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Myotonic Dystrophy Foundation Announces Launch of Medical Website and Online Community for Myotonic Dystrophy
[September 18, 2008]

Myotonic Dystrophy Foundation Announces Launch of Medical Website and Online Community for Myotonic Dystrophy


(Marketwire Via Acquire Media NewsEdge) ROCKLIN, CA, September 18 / MARKET WIRE/ --

The Myotonic
Dystrophy Foundation (MDF), a patient advocacy organization, is excited
to announce the launch of its long-awaited website, www.myotonic.com. It
offers expansive information to help affected families understand and cope
with this complex, multisystemic disorder. The primary mission of the MDF
focuses on education (for families and medical providers), advocacy and
research. All disease information on the website has been edited and
approved by members of the MDF Medical
and Scientific Advisory Committee comprised of American experts in the
field of myotonic dystrophy and muscle research. In addition, the MDF has
launched a community site, www.community.myotonic.com, where individuals
can meet others living with similar challenges and share information.

Myotonic
dystrophy is a common form of muscular dystrophy that can appear at any
time from birth to old age. It affects approximately 1:8000 people
worldwide. Myotonic dystrophy is also a multisystemic disorder affecting
not only muscles but also many systems in the body, including the heart,
brain, respiratory and endocrine systems and GI tract, among others. It is
described as "...the most variable disorder known in medicine," and is
commonly misdiagnosed by doctors. Since the gene was identified in the
early 1990s, researchers have discovered that the genetic flaw generally
enlarges and causes more severe symptoms in subsequent generations at an
earlier age. The transmission of a more severe form at an earlier age,
called anticipation, indeed renders myotonic dystrophy a genetic time bomb.

The site offers information about the disease, with a more in-depth


description for practitioners in the Professionals
section; it offers a medical glossary, resources and links, FAQs,
multisystemic features, disease mechanism, MDF postdoctoral fellowship awards (awards to be made annually

beginning in January, 2009 -- $100,000 over two years for two researchers),
family stories, advocacy news, and ways to get involved. The community site
enables affected family members to communicate with others traveling the
same path.


For more information about the MDF websites, contact Lisa Vittek, Managing
Director, Myotonic Dystrophy Foundation, [email protected].

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Contact:
Lisa Vittek
Managing Director
Myotonic Dystrophy Foundation
Phone: 86-MYOTONIC or (866) 968-6642
E-mail: [email protected]

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