I just read where it is said that the FDA Maude Data base 08/02 has 18 adverse reaction reports regarding interstim. That cannot be as there are more than that with adverse reactions in my area of the country alone,several known in Michigan for sure and I have a manila envelope full of hundreds of adverse reaction reports with each person's serial number of their implanted device. That information must be talking of something else with these and for some reason not pertaining to all the adverse reaction reports filed already with the FDA..there are at least 10 injuries of a serious nature in Denver alone,then all the gals in Michigan and several in my state as well as all over the nation. Anyone can call or write the FDA and get copies of these reports and see just how serious some of the damages from the interstim are.