Someone else brought this up on another website and did not want to ask but leaves my thoughts unsettled. According to memory, the Tnbc study lasted approx. one year? Were all the surviving patients allowed to continue using LL if they wished. Did the FDA letter cut their ability to use LL? If their supply of LL was cut off, would results be even greater if they received LL continually after study ended or did the study never end and are receiving LL NOW? .