I don't know of a direct substitute for LAH. But there is almost always an alternatice synthetic way. Think of the nitrostyrene reduction: Shulgin uses LAH all the time. but you can also do it with [NaBH4 + NiCl2] or electrolytically or first reduce the double bond with NaBH4, then the nitro group. Or you could go the phenylethanol --> phenylethyl-iodid --> PEA way... this is what I love about organic chemistry.
--psyloxy--