We report rheology and structural studies of poly(lactide)-poly(ethylene oxide)-poly(lactide) (PLA-PEO-PLA) triblock copolymer gels with various ratios of l-lactide and d-lactide in the PLA blocks. These materials form associative micellar gels in water, and previous work has shown that stereoregular triblocks with a l/d ratio of 100/0 form much stiffer gels than triblocks with a 50/50 l/d ratio. Our systems display an unexpected maximum in the storage modulus, G', of the hydrogels at intermediate l/d ratio. The impact of stereochemistry on the rheology is very striking; gels with an l/d ratio of 85/15 have storage moduli that are ∼1-2 orders of magnitude higher than hydrogels with l/d ratios of 100/0. No stereocomplexation is observed in the gels, although PLLA crystals are found for gels with l/d ratios of 95/5 and 90/10, and SANS results show a decrease in the intermicellar spacing for intermediate l/d ratios. We expect the dominant contribution to the elasticity of the gels to be intermicellar bridging chains and attribute the rheology to a competition between an increase in the time for PLA endblocks to pull out of micelles as the l/d ratio is increased and PLLA crystallization occurs, and a decrease in the number of bridging chains for micelles with crystalline PLA domains, as formation of bridges may be hindered by crowded crystalline PLA domains. These results provide a new strategy for controlling the rheology of PLA-based hydrogels for potential applications in biomaterials, as well as fundamental insights into how intermicellar interactions can be tuned via stereochemistry.