California Lyme Disease Association (CALDA) reports this extremely frustrating and disappointing news on the fight for fair and balanced guidelines for treating Chronic Lyme Disease and other tick -borne diseases. i really hope President Obama will do something about the unfairness of the Infectious Disease Society of America (IDSA). i hate that these people are in bed with drug companies and insurance companies where it is ALL about money and their own interests rather that the health and well-being of those who are chronically ill, like moi!
Greenwich, CT, January 28, 2009-Patient groups voiced concern and disappointment about the new Infectious Diseases Society of America (IDSA) Lyme disease guidelines’ panel, which excludes physicians who treat patients with chronic Lyme disease. Last May, the Connecticut Attorney General found the IDSA Lyme disease treatment guidelines’ panel had conflicts of interest, engaged in exclusionary conduct, and suppressed scientific evidence. The investigation resulted in a settlement forcing the IDSA to reconstitute a balanced panel free of conflicts of interest under the oversight of an ombudsman to monitor conflicts of interest. No input from patients or treating physicians was permitted in selection.
“This situation is déja vu all over again,” said national Lyme Disease Association president Pat Smith about the newly created guidelines’ panel. “All Lyme disease treating physicians who applied for a seat were denied, based on having a “conflict” if they made over $10,000 treating Lyme disease. They have confused helping patients get better with ‘real’ competing conflicts such as interests in testing and vaccines, and relationships with insurers−a profile found in the original panel. Physicians who treat understand what makes patients well.”
Attorney Lorraine Johnson of the California Lyme Disease Association points out “The problem is that guidelines conclusions generally reflect panel composition. That is why it is critical that a panel be balanced and include different points of view. Excluding the point of view of physicians who treat chronic Lyme disease makes no sense and biases this panel.”
READ the rest here.
