Dear Dr. Fine, I'm a 34-year old woman recently diagnosed with a digestive disorder that caused me to be mostly bedridden for 4 years. Today, I'm preparing to go back to work. Ten years ago, I enjoyed physically demanding sports like mountain biking, had just earned an MBA from a top-ten business school, and was working for a high technology company. By the time I turned 30, my body had become so weak that brushing my hair drained me, my handwriting was illegible, and I began having trouble with reading comprehension and memory. It took eight years to get the diagnosis of gluten intolerance, which I got from Dr. Fine's lab, Enterolab. Only a few months later, I was rapidly recovering by adhering to the only treatment for this condition, a life-long gluten-free diet. Before I went on the gluten-free diet, my list of symptoms was long and varied, but I could summarize it as a constant feeling that I had the flu or was about to come down with the flu. I slept 14 hours a night and was still exhausted in the day. My cognitive dysfunction and memory problems made me feel as if I'd suddenly lost 20 IQ points. I also suffered from nausea, fevers, arthritis, and a permanent migraine-like headache. I was constantly on antibiotics for sinus and bladder infections. I also had excessive flatulence and gastrointestinal pain, which didn't make my top 10 list of complaints, but would later turn out to be the key to my cure. Hindering my diagnosis, the only abnormal lab tests I had were anemia and a low white blood cell count. The last year I was able to work full-time was 1996. Saying I worked "full-time" is stretching the truth a little given that my ever-worsening health had reduced me to a maximum of 2 to 3 days a week. Finally I got so ill that I never felt well again. I searched frantically for what was wrong with me so I could be cured and continue on my career track. After consulting more than 10 doctors, one of them offered a diagnosis of Chronic Fatigue Syndrome. Although this diagnosis didn't explain all the medical problems I had, it classified me as "disabled" and allowed me to take a much-needed medical leave until I was well enough to work again. So began my struggle to get my life back and my quest to find out what was really wrong with me. After my first year of disability, I was diagnosed with lupus. I wouldn't know until a few years later that this was only part of the story. I was elated to have a diagnosis that finally seemed to explain everything I was going through, and I was delighted to ditch the oft-criticized Chronic Fatigue Syndrome label. For the next few years I treated the lupus through medication and alternative therapies. It helped a little but I was still only a fraction of my formerly active self. Finally, a few years after that, I stumbled upon my real medical problem, gluten intolerance. I discovered how to control what I thought was my most minor, but socially embarrassing health problem, excessive gas. If I didn't eat wheat -- no bread, pasta, cakes, or cookies -- I didn't have gas or stomach cramps. I went to my gastroenterologist to share this new information. Indigestion after eating wheat is a textbook symptom of gluten intolerance & celiac disease, but even the gastroenterologist told me it was just Irritable Bowel Syndrome and that no diet change was necessary. Since I was much happier without the gas and stomach pains, I stuck with the wheat-free diet, purely for the sake of being gas-free. To my amazement, my other health problems began to disappear after two months without wheat. First, I noticed I was feeling less nauseated than before and hadn't run a fever for a while. Then, my arthritis cleared up. Soon my headaches were a thing of the past. I was sleeping 11 hours a night instead of 14. I realized I hadn't had to take antibiotics for a few months which was a breakthrough after 10 years of starting a course of antibiotics every 4 to 6 weeks for constant sinus and bladder infections. My cognitive abilities started slowly returning. I had many other minor problems, like horrible menstrual cramps and manual dexterity problems. These literally vanished as well. I knew I had finally found my cure in the wheat-free diet, but I still didn't know that I had gluten intolerance. Through research on the internet, I learned that I might have celiac disease and went on a strict gluten-free diet. I went back to my gastroenterologist, reported on my progress, and asked to be tested for it. He agreed, but insisted (incorrectly) that I didn't have to be eating wheat for the celiac blood tests to be accurate. Sure enough, since I'd been on a gluten-free diet for 4 months, the blood tests came back negative. Finally, through more research, I found EnteroLab and sent in my stool sample for testing. Their lab showed that despite being gluten-free, I did indeed have many gluten anti-bodies and that I had a gene that causes celiac disease. Finally, eight years after my symptoms began, I had the answer to all my health problems. Most importantly, I'm off all medications and am well for the first time in eight years. Today, I'm getting ready to return to work and am leading an increasingly active lifestyle. My doctors say that my lupus never would have been active if, earlier in my life, I'd been diagnosed with gluten intolerance, and followed the gluten-free diet. Since my diagnosis, five of my family members have tested positive for the disease. My cousin went on the gluten-free diet and her monthly epileptic seizures suddenly stopped. She is off anti-seizure medication and hasn't had a seizure for over a year now. The diet also cured her lupus and arthritis. Our success is motivating many others to investigate the gluten connection for themselves. Maybe my story will help you, too.