Search Canlyme site Home Symptoms Live Discussion Diagnosis Treatment World-wide Support Finder Books/Video RESEARCH Lymelinks Contact Pets & Lyme DONATIONS Drug Info Medical Dictionary Board of Directors      Click on the graphic to vote for this site as a Starting Point Hot Site. No Warranties or Representations Lyme Disease symptoms vary from person to person. (lymes disease lyme's disease lime disease limes disease) The data and information presented in this web site are presented in good faith and believed to be accurate regarding Lyme disease (commonly misspelled lymes disease lyme's disease lime disease limes disease) and other related diseases. Any and all liability for the content or any omissions including any inaccuracies, errors, or misstatements in such data or information is expressly disclaimed. The web site is compiled for the sole purpose of informing community members of resources and information pertaining to Lyme Borreliosis Disease and its coinfections. Lyme disease symptoms may vary from person to person. The Canadian Lyme Disease Foundation, Directors and members are not liable for any direct or indirect damages or any damages whatsoever resulting from loss of use, data or profits, whether in an action of contract, negligence or other tortious action arising out of or in connection with the use or performance of information available from this website. Consult a qualified Lyme ( Borreliosis ) Disease literate doctor for medical advice if Lyme Disease is suspect to discuss your Lymes Disease Symptoms. en français For Physicians Ticks Coinfections Prevention Our Stories Click Here to order our free Lyme Disease Flyer,    Here for our free Lyme Disease Poster ..documents may be copied (to distribute) but edit only for alignment. Books/Video on Lyme Disease http://www.nj. com/business/ ledger/index. ssf?/base/ business- 6/11773939581314 00.xml&coll= 1 The Star Ledger Burning Questions Tuesday, April 24, 2007 Pat Smith is president of the Lyme Disease Association, a national group based in Jackson Township. What makes the new Lyme & Tick-Borne Diseases Research Center at Columbia University Medical Center different from other Lyme centers? This is the first endowed center of its kind in the world to study chronic Lyme disease and other tick-borne diseases. For too long, it's been said the doctors treating patients for long-term Lyme disease don't have science on their side. We totally disagree with that, but now this university-based center will have distinguished scientists who will examine all aspects of chronic Lyme. What will they be looking at? One study will study the neuropathology of the brain and look at brain tissue of patients with chronic Lyme. The center will look at new diagnostic tests, co-infections, genetic markers of vulnerability and immunopathogenesis, among others. Is there still controversy over whether long-term Lyme exists? We don't feel there is controversy anymore. But there are still some diehards in the medical field who feel that chronic Lyme disease is not an entity. They don't feel these patients have chronic disease. But that certainly is changing, and we are trying to demonstrate change through cutting-edge research. We feel this center will make a huge leap in that direction. How much did the center cost, and where did the money come from? We raised $3 million. It came from the Lyme Disease Association and the Connecticut- based Time For Lyme (TFL), who were partners in the creation of the center at Columbia. We've worked five years to make this happen, and we are very excited. When does the center open? Monday, April 30. -- Carol Ann Campbell TOP