Until the advent of the novel Enders catalysts, the nonlinear rheological characterization of polyethylene (PE) blends, containing up to 50 wt. % of ultra-high molecular weight PE (UHMWPE, with weight average molecular weight M-w > 10(6) g/mol) was unattainable. In this study, by melt blending of a commercially available high-density PE (polymer matrix) and PE-reactor-blends (RBs), multimodal PE blends were prepared, and their nonlinear viscoelastic properties were investigated. The experiments revealed how extraordinarily high amount of UHMWPE content and ultra-broad molecular weight distribution characterized by well separated molecular weight modes influence the nonlinear viscoelasticity. Furthermore, in order to evaluate the strain hardening ability of the multimodal PE, an approach was proposed allowing to objectively analyze and quantify the nonlinear response of the investigated samples. Analyzing the "state diagram" of the extended specimens, which captures the melt behavior and flow instabilities during uniaxial extensional measurements, unveiled that the observed SH of multimodal PE blends, at temperatures notably higher than their melting temperature, is controlled by the stretched chains of the 2nd well separated UHMWPE molecular weight mode. Moreover, it was found that, in order to highly stretch the PE chains, a characteristic strain must be applied.