Under Our Skin Shows Patients and Physicians Fighting for Lives and Livelihoods
� Does Chronic Lyme exist?
� Lyme misdiagnosed as M.S., ALS, Parkinson's?
� Medical establishment disavows diagnosis and long-term treatment.
� Doctors who treat patients are penalized.
(Fort Lauderdale, FL) - There has been an alarming jump in Lyme disease cases - nearly a 40% increase nationwide. Lyme Disease may be the most controversial illness in America today. It's certainly among the most misunderstood. Is it easily treated with a short course of antibiotics or can it be a long term (or chronic) illness that's increasingly misdiagnosed--leading to lifelong disabilities and even death?
Now an acclaimed new documentary, Under Our Skin, examines the debilitating truths about Lyme disease. Tens of thousands of victims either go undiagnosed or believe they are misdiagnosed with such conditions as multiple sclerosis, Lou Gehrig's disease, Parkinson's disease, fibromyalgia, chronic fatigue, autism and even hypochondria. In heartbreaking detail, Under Our Skin chronicles patients' long and frustrating battles against both the illness and a skeptical medical establishment.
Almost everyone knows someone who suffers from Lyme. Transmitted by ticks, the number of cases in the United States has doubled since 1991--with at least 27-thousand new cases each year. But the Centers for Disease Control admits the actual numbers may be up to twelve times higher--making Lyme disease an epidemic larger than AIDS, West Nile Virus and Avian Flu combined. Yet there is no accurate test to diagnose the disease, and the medical community is at odds on how to treat it. Many doctors deny Chronic Lyme exists and insurance companies often refuse to pay for long term medical treatment.
In Under Our Skin, Andy Abraham Wilson and Open Eye Pictures investigate the human, medical and political dimensions of Lyme disease. Years in the making, the film brings into focus a haunting picture of our healthcare system and its ability (or inability) to cope with a silent terror under our skin.
``The most important documentary to come out this year.''--Molly Bedham, XM Radio
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
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