We give a brief review of how activation energies from scan-rate- dependent T-g studies have been correlated with those for viscosity and other relaxation processes, in order to place the present study in context with previous work, including that referred to in the comment. Then we examine the ensuing question of the extent to which kinetic fragility can be predicted from thermodynamic data. We present a new correlation involving only the entropy of fusion and the jump in heat capacity at T-g, that is followed by most nonchain liquids. Polymer liquids, as the comment authors have shown, have different behavior, consistent with earlier failures to identify Kauzmann and Vogel temperatures in these materials. (C) 2003 American Institute of Physics.