My CFS/fibromyalgia was actually LYME

After 20 years of misdiagnosis, I finally got an accurate diagnosis. This enabled me to start targeting my treatment correctly. I really believe there are tons of folks out there being told they have cfs/fibro, when it's caused by lyme or a lyme coinfection. Folks, it is my understanding that lyme has spread throughout the country and even throughout the world. It can be passed my a mosquito bite. I often see the word epidemic associated with lyme now. How many people are walking with it without knowing? Please consider being tested. It's worth it to rule out lyme. Please note that the mainstream tests (western blot) has a huuuuuge percentage of false negatives.

Here is a link to an article with the newer testing info (labs and tests) and alternative treatment resources.

http://www.successfulhealing.com/Lyme-Disease-Specific-Wellness-Pla...