The crystallization of glasses and amorphous solids is studied in many fields to understand the stability of amorphous materials, the fabrication of glass ceramics, and the mechanism of biomineralization. Recent studies have found that crystal growth in organic glasses can be orders of magnitude faster at the free surface than in the interior, a phenomenon potentially important for understanding glass crystallization in general. Current explanations differ for surface-enhanced crystal growth, including released tension and enhanced mobility at glass surfaces. We report here a feature of the phenomenon relevant for elucidating its mechanism: Despite their higher densities, surface crystals rise substantially above the glass surface as they grow laterally, without penetrating deep into the bulk. For indomethacin (IMC), an organic glass able to grow surface crystals in two polymorphs (α and γ), the growth front can be hundreds of nanometers above the glass surface. The process of surface crystal growth, meanwhile, is unperturbed by eliminating bulk material deeper than some threshold depth (ca. 300 nm for α IMC and less than 180 nm for γ IMC). As a growth strategy, the upward-lateral growth of surface crystals increases the system's surface energy, but can effectively take advantage of surface mobility and circumvent slow growth in the bulk. C rystallization is a ubiquitous process, producing countless solids in the natural and man-made world. Glasses and amorphous solids are formed by avoiding crystallization while cooling liquids, condensing vapors, or drying solutions. The solidity of a glass might suggest resistance to crystallization; its very existence implies that crystallization is avoidable. And yet glasses can crystallize, sometimes surprisingly fast. The crystallization of glasses is of interest in many fields for understanding the stability of amorphous materials (1), the fabrication of glass ceramics, and the mechanism of biomineralization, for which crystallization of amorphous solid precursors is considered a key step (2).Recent studies have discovered that different modes of crystal growth can emerge as a liquid is cooled to form a glass (3-8), causing crystal growth fronts to advance at velocities much faster than predicted by standard theories. One such growth mode [the glass-to-crystal (GC) mode] exists in the bulk and can cause an increase of crystal growth rate by a factor of 10 4 with a temperature drop by a few kelvin (3, 4). Another new growth mode occurs at the free surface and can lead to much faster crystal growth than in the bulk (5-8). Although these phenomena have been observed prominently in organic glasses, they may be relevant for understanding glass crystallization in general. These phenomena seem to have counterparts in nonorganic glasses, but differences are also evident. Fast crystal growth is known for metallic glasses and amorphous silicon, but the abrupt activation of GC growth is reported only for organic glasses. Surface-enhanced crystal growth occurs in amorphous selenium ...