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Hydride-forming alloys are currently considered reliable and suitable hydrogen storage materials because of their relatively high volumetric densities, and reversible H2 absorption/desorption kinetics, with high storage capacity. Nonetheless, their practical use is obstructed by several factors, including deterioration and slow hydrogen absorption/desorption kinetics resulting from the surface chemical action of gas impurities. Lately, common strategies, such as spark plasma sintering, mechanical alloying, melt spinning, surface modification and alloying with other elements have been exploited, in order to overcome kinetic barriers. Through these techniques, improvements in hydriding kinetics has been achieved, however, it is still far from that required in practical application. In this review, we provide a critical overview on the effect of mechanical alloying of various metal hydrides (MHs), ranging from binary hydrides (CaH2, MgH2, etc) to ternary hydrides (examples being Ti-Mn-N and Ca-La-Mg-based systems), that are used in solid-state hydrogen storage, while we also deliver comparative study on how the aforementioned alloy preparation techniques affect H2 absorption/desorption kinetics of different MHs. Comparisons have been made on the resultant material phases attained by mechanical alloying with those of melt spinning and spark plasma sintering techniques. The reaction mechanism, surface modification techniques and hydrogen storage properties of these various MHs were discussed in detail. We also discussed the remaining challenges and proposed some suggestions to the emerging research of MHs. Based on the findings obtained in this review, the combination of two or more compatible techniques, e.g., synthesis of metal alloy materials through mechanical alloying followed by surface modification (metal deposition, metal-metal co-deposition or fluorination), may provide better hydriding kinetics.