I've noticed alot of people mentioning positive results with T3, and it's second only to LDN on curetogether's CFS treatment survey for medical treatments. I have some questions for those experienced with it (this refers to T3-only, not T4 or dessicated thyroid): Did you have lab evidence suggesting a need for T3 prior to starting (low free T3, high reverse T3, etc)? What does your protocol look like, in terms of form (cytomel vs compounded SR T3), dosage, times per day, etc? What do you think of Dr. Cheney's opinion that T3 is "the worst hormone you can give a CFS patient"? BS? Does your doctor express an opinion on it? What effects, positive or negative, have you noted from T3 treatment?