Creep experiments were carried out on amorphous selenium (Se) at temperatures in the vicinity of the glass temperature. The recoverable compliance lacks a plateau, indicating Se chains are too short to form an entanglement network. The measured compliance function was thermorheological complex, even after subtraction of the glassy level and normalizing by the steady state compliance. The temperature dependence determined from the viscosity was in accord with previous viscosity data, although weaker than the near-Arrhenius dependence deduced from the stress relaxation of Se. Based on a comparison to other, small-molecule glass-formers, the dynamic fragility calculated from the viscosity was larger than expected from Se's thermodynamic fragility (i.e., steepness of the normalized Kauzmann curve). In contrast, although polypropylene (PP) is substantially more dynamically fragile than Se, PP is less thermodynamic fragile. Thus, when compared to either small-molecule liquids or polymers, Se exhibits a disconnect between dynamic and thermodynamic measures of fragility.