New Johns Hopkins Lyme Disease Clinical Research Center launched

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Press Release: Johns Hopkins, May 14, 2015. Fundamental research into the causes and cures of post-treatment Lyme disease syndrome now has its first home base at a major U.S. medical research center with the launch of the Johns Hopkins Lyme Disease Clinical Research Center. Inaugurated on May 12, 2015, with a major gift from the Lyme Disease Research Foundation, the center plans an ambitious research program targeting this increasingly common disease, which costs the U.S. economy up to $1.3 billion per year in treatment costs alone.
First discovered in Lyme, Connecticut, 40 years ago, Lyme disease has spread rapidly throughout the East Coast and Midwest. It now afflicts more than 300,000 people per year, becoming the sixth most common reportable infectious disease in the U.S.
“If you live anywhere from Maine to Virginia, it’s almost impossible for Lyme disease not to affect someone you know, someone in your family or yourself,” says center founder and director John Aucott, M.D., a Johns Hopkins internist. Aucott, an assistant professor of medicine at Johns Hopkins, has spent more than a decade studying the disease’s potentially crippling effects.
When a tiny tick infected with the bacterium Borrellia burgdorferi bites a human, that person may develop symptoms that seem flu-like, such as swollen glands, fatigue, body aches and rashes. Most people respond well to antibiotics. But about one out of every five or six patients develops a debilitating condition called post-treatment Lyme disease syndrome, marked by extreme fatigue; musculoskeletal pain; arthritislike pain in the joints; and cognitive, neurological and cardiac syinfectious diseasemptoms. [sic]

“This syndrome is not fatal, but it is life-altering,” says Aucott. “People who come down with Lyme disease are active people who have the bad luck to be bitten by an infected tick while they’re out hiking, camping or mowing the grass. It can happen to anyone anywhere there are trees, deer and the ticks that they carry.”
As director of the new clinical research center, housed at Johns Hopkins Bayview Medical Center, Aucott has received an initial grant to lead the first prospective controlled study in the U.S. to examine the impact of Lyme disease on patients’ immune systems and their long-term health. Known as SLICE (Study of Lyme Disease Immunology and Clinical Events), the study aims to understand why some patients develop post-treatment Lyme disease syndrome lasting months or years, while others do not.
The Lyme Disease Research Foundation has also helped establish repositories of blood and tissue samples from patients with Lyme disease at Johns Hopkins, providing researchers with opportunities to collaborate in the search for disease biomarkers that could lead to improved diagnostics and treatment.
The Johns Hopkins Lyme Disease Clinical Research Center will act as a hub for catalyzing the exploration of Lyme disease. Securing funding for the center will be critical to future discoveries in Lyme disease.

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2 thoughts on “New Johns Hopkins Lyme Disease Clinical Research Center launched”

  1. prohealth4scott says:

    What is this research center 4 Lyme disease is easily cured. I want to know when those responsible for all the suffering associated with this life destroying disease are going to be held responsible?

  2. lymewarrior58 says:

    I THOUGHT this was going to be a move in the right direction but once again, hopes dashed. “Post lyme disease syndrome?” Spare me….looks like even John Hopkins is caving-in to the IDSA’s verbiage. Why? Because if the name it “Chronic Lyme Disease” that would mean they (the CDC along with the IDSA) would have to admit that this disease is CONTINUAL and they don’t want to do that. Again, why? Because it would cost the health care system billions of dollars to treat us, not to mention all the other costs since CHRONIC LYME DISEASE….us “few” poor soul’s that don’t get better “easily,” can’t work and since the CDC refuses to classify this as an on-going disease, getting social security is close to impossible, most have to go on food stamps and fuel assistance, we lose most friends, family’s fall apart, and the list goes on and on….and they don’t want to pay any of it.

    Why is it that lyme disease has one of, if not THE highest suicide rate of any illness (presently at approximately 58%) and yet no outcry????

    I’m extremely happy with this news for those who come behind us, but unless all the infighting stops, the patents by Yale shared, some government funding for research, and an outcry from the news outlets, we will remain in the shadows slowly dying or taking our lives because we can’t live another day in this horror-show.

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