The segmental and local dynamics of semicrystalline, melt-miscible blends of poly(ethylene oxide) [PEO] and a poly(styrene-co-p-hydroxystyrene) copolymer [SHS] were investigated using dielectric relaxation spectroscopy (DRS). A broad, yet well-defined, DRS segmental process is observed for the 5 wt % SHS blend, and it gradually shifts to higher temperature and broadens further with increasing SHS content. It can be distinguished in the 3D spectrum of the 10 wt % SHS blend, but it is only barely discernible in the spectrum of the 15 wt % SHS blend, as it is masked by large low frequency losses likely arising from electrode polarization. On the basis of current and previous findings, we propose that the observed segmental process is comprised of a slower cooperative segmental relaxation involving both components, as well as a faster process due to less associated PEO segments. Furthermore, heterogeneous spatial distribution of the SHS segments also promotes broadening of the segmental process in these blends, particularly at higher SHS contents. Hydrogen-bonded hydroxystyrene units produce a beta(S1) process, which is more cooperative than typical local relaxations, in light of its activation energy and the temperature insensitivity of its relaxation strength. All blends exhibit a high-frequency gamma(b) relaxation, near the gamma(PEO) and SHS beta(S2) processes of the neat components. The f-T locations of the gamma(b) relaxation in the various blends are the same within experimental error, and they are closer to the gamma(PEO) than to SHS beta(S2) process.