BYF!

i rt a lot, i curse, i’m sometimes nsfw, i’m nd and fuckin old so sometimes i won’t use a phrase correctly 😭, i use emoji’s, i will tone indicate sometimes, delete tweets, i fb +18 but only if your pronouns and age are in your bio/carrd, i post a lot about astrology in regards to kpop bc both are special interests but i understand they can be annoying

DFI!

under 18, anti any race/muslim/lgbt, minor, not comfortable with me at all, anti any of my ults

skz, nct, svt, ateez, p1harmony, bts, blackpink mx, e’last, txt, itzy, oneus

sabrina carpenter, sza, renee rapp, 5sos, icon for hire, paramore, rihanna, taylor swift

shay, sunny, vi, kris, gaby, yas, jess,
sof, tori

bang chan

bang chan, yuta, kun, shownu, seonghwa, jeonghan, jisoo, keeho, namjoon, choi in, yeonjun, yeji

𝚃𝚆// 𝙸 𝚠𝚒𝚕𝚕 𝚋𝚎 𝚍𝚒𝚜𝚌𝚞𝚜𝚜𝚒𝚗𝚐 𝚖𝚢 𝚊𝚞𝚝𝚘𝚒𝚖𝚖𝚞𝚗𝚎 𝚍𝚒𝚜𝚎𝚊𝚜𝚎 𝚠𝚑𝚒𝚌𝚑 𝚒𝚗𝚌𝚕𝚞𝚍𝚎𝚜 𝚝𝚊𝚕𝚔𝚒𝚗𝚐 𝚊𝚋𝚘𝚞𝚝 𝚋𝚕𝚘𝚘𝚍 𝚊𝚗𝚍 𝚌𝚑𝚎𝚖𝚘 𝚝𝚛𝚎𝚊𝚝𝚖𝚎𝚗𝚝𝚜. 𝙸𝚏 𝚢𝚘𝚞 𝚊𝚛𝚎 𝚝𝚛𝚒𝚐𝚐𝚎𝚛𝚎𝚍 𝚋𝚢 𝚝𝚑𝚎𝚜𝚎 𝚝𝚑𝚒𝚗𝚐𝚜, 𝚙𝚕𝚎𝚊𝚜𝚎 𝚌𝚕𝚒𝚌𝚔 𝚊𝚠𝚊𝚢. <𝟹𝙶𝙿𝙰 𝚘𝚛 𝙶𝚛𝚊𝚗𝚞𝚕𝚘𝚖𝚊𝚝𝚘𝚜𝚒𝚜 𝚠𝚒𝚝𝚑 𝚙𝚘𝚕𝚢𝚊𝚗𝚐𝚒𝚒𝚝𝚒𝚜 𝚒𝚜 𝚊 𝚛𝚊𝚛𝚎 𝚊𝚞𝚝𝚘𝚒𝚖𝚖𝚞𝚗𝚎 𝚍𝚒𝚜𝚎𝚊𝚜𝚎 𝚝𝚑𝚊𝚝 𝙸 𝚠𝚊𝚜 𝚍𝚒𝚊𝚐𝚗𝚘𝚜𝚎𝚍 𝚠𝚒𝚝𝚑 𝚝𝚑𝚒𝚜 𝚢𝚎𝚊𝚛. 𝙸𝚝 𝚒𝚜 𝚕𝚒𝚔𝚎 𝚖𝚘𝚜𝚝 𝚊𝚞𝚝𝚘𝚒𝚖𝚖𝚞𝚗𝚎 𝚍𝚒𝚜𝚎𝚊𝚜𝚎𝚜 𝚒𝚗 𝚝𝚑𝚊𝚝 𝚛𝚊𝚝𝚑𝚎𝚛 𝚝𝚑𝚊𝚝 𝚢𝚘𝚞𝚛 𝚒𝚖𝚖𝚞𝚗𝚎 𝚜𝚢𝚜𝚝𝚎𝚖 𝚠𝚘𝚛𝚔𝚒𝚗𝚐 𝚝𝚘 𝚙𝚛𝚘𝚝𝚎𝚌𝚝 𝚘𝚗𝚎𝚜 𝚋𝚘𝚍𝚢 𝚏𝚛𝚘𝚖 𝚐𝚎𝚝𝚝𝚒𝚗𝚐 𝚜𝚒𝚌𝚔, 𝚝𝚑𝚎 𝚒𝚖𝚖𝚞𝚗𝚎 𝚜𝚢𝚜𝚝𝚎𝚖 𝚊𝚝𝚝𝚊𝚌𝚔𝚜 𝚍𝚒𝚏𝚏𝚎𝚛𝚎𝚗𝚝 𝚙𝚊𝚛𝚝𝚜 𝚘𝚏 𝚝𝚑𝚎 𝚋𝚘𝚍𝚢, 𝚞𝚜𝚞𝚊𝚕𝚕𝚢 𝚘𝚛𝚐𝚊𝚗𝚜. 𝙶𝙿𝙰 𝚖𝚘𝚜𝚝 𝚘𝚏𝚝𝚎𝚗 𝚊𝚝𝚝𝚊𝚌𝚔𝚜 𝚝𝚑𝚎 𝚕𝚞𝚗𝚐𝚜 𝚊𝚗𝚍 𝚝𝚑𝚎 𝚔𝚒𝚍𝚗𝚎𝚢𝚜. 𝚃𝚑𝚎 𝚜𝚢𝚖𝚙𝚝𝚘𝚖𝚜 𝚞𝚜𝚞𝚊𝚕𝚕𝚢 𝚙𝚛𝚎𝚜𝚎𝚗𝚝 𝚕𝚒𝚔𝚎 𝚊 𝚌𝚘𝚕𝚍 𝚋𝚞𝚝 𝚕𝚊𝚜𝚝 𝚕𝚘𝚗𝚐 𝚊𝚗𝚍 𝚠𝚒𝚝𝚑 𝚊 𝚏𝚎𝚠 𝚖𝚘𝚛𝚎 𝚊𝚋𝚗𝚘𝚛𝚖𝚊𝚕𝚒𝚝𝚒𝚎𝚜. 𝙾𝚗𝚎 𝚘𝚏 𝚖𝚢 𝚜𝚢𝚖𝚙𝚝𝚘𝚖𝚜 𝚏𝚘𝚛 𝚎𝚡𝚊𝚖𝚙𝚕𝚎, 𝚠𝚊𝚜 𝚌𝚘𝚞𝚐𝚑𝚒𝚗𝚐 𝚞𝚙 𝚋𝚕𝚘𝚘𝚍. 𝙶𝙿𝙰 𝚠𝚒𝚕𝚕 𝚊𝚕𝚜𝚘 𝚌𝚊𝚞𝚜𝚎 𝚓𝚘𝚒𝚗𝚝 𝚙𝚊𝚒𝚗 𝚒𝚗 𝚙𝚊𝚝𝚒𝚎𝚗𝚝𝚜.𝙶𝙿𝙰 𝚒𝚜 𝚊 𝚝𝚢𝚙𝚎 𝚘𝚏 𝚟𝚊𝚜𝚌𝚞𝚕𝚒𝚝𝚒𝚜, 𝚖𝚎𝚊𝚗𝚒𝚗𝚐 𝚒𝚗𝚏𝚕𝚊𝚖𝚖𝚊𝚝𝚒𝚘𝚗 𝚒𝚗 𝚝𝚑𝚎 𝚋𝚕𝚘𝚘𝚍 𝚟𝚎𝚜𝚜𝚎𝚕𝚜. 𝙼𝚒𝚗𝚎 𝚘𝚌𝚌𝚞𝚛𝚜 𝚒𝚗 𝚝𝚑𝚎 𝚜𝚖𝚊𝚕𝚕 𝚟𝚎𝚜𝚜𝚎𝚕𝚜. 𝚆𝚑𝚎𝚗 𝚝𝚑𝚎𝚛𝚎 𝚒𝚜 𝚜𝚠𝚎𝚕𝚕𝚒𝚗𝚐 𝚒𝚗 𝚝𝚑𝚎 𝚟𝚎𝚜𝚜𝚎𝚕𝚜, 𝚒𝚝 𝚛𝚎𝚜𝚝𝚛𝚒𝚌𝚝𝚜 𝚋𝚕𝚘𝚘𝚍 𝚏𝚕𝚘𝚠 𝚝𝚘 𝚝𝚑𝚎 𝚘𝚛𝚐𝚊𝚗𝚜, 𝚜𝚙𝚎𝚌𝚒𝚏𝚒𝚌𝚊𝚕𝚕𝚢 𝚝𝚑𝚎 𝚕𝚞𝚗𝚐𝚜 𝚊𝚗𝚍 𝚔𝚒𝚍𝚗𝚎𝚢𝚜.𝙶𝙿𝙰 𝚒𝚜 𝚖𝚘𝚜𝚝 𝚘𝚏𝚝𝚎𝚗 𝚏𝚘𝚞𝚗𝚍 𝚒𝚗 𝚊𝚍𝚞𝚕𝚝𝚜 𝚊𝚐𝚎𝚜 𝟻0-𝟼0 𝚊𝚗𝚍 𝚝𝚑𝚎𝚛𝚎 𝚊𝚛𝚎 𝚏𝚎𝚠𝚎𝚛 𝚝𝚑𝚊𝚗 𝟸00,000 𝚌𝚊𝚜𝚎𝚜 𝚒𝚗 𝚝𝚑𝚎 𝚄𝚂 𝚎𝚊𝚌𝚑 𝚢𝚎𝚊𝚛. 𝚃𝚑𝚎𝚛𝚎 𝚒𝚜 𝚗𝚘 𝚌𝚞𝚛𝚎 𝚏𝚘𝚛 𝚝𝚑𝚘𝚜𝚎 𝚠𝚒𝚝𝚑 𝚝𝚑𝚎 𝚍𝚒𝚜𝚎𝚊𝚜𝚎 𝚋𝚞𝚝 𝚝𝚑𝚎𝚛𝚎 𝚊𝚛𝚎 𝚝𝚛𝚎𝚊𝚝𝚖𝚎𝚗𝚝𝚜. 𝙸 𝚙𝚎𝚛𝚜𝚘𝚗𝚊𝚕𝚕𝚢 𝚝𝚊𝚔𝚎 𝚊 𝚖𝚎𝚍𝚒𝚊𝚝𝚒𝚘𝚗 𝚝𝚑𝚊𝚝 𝚒𝚜 𝚞𝚜𝚎𝚍 𝚏𝚘𝚛 𝚘𝚛𝚐𝚊𝚗 𝚍𝚘𝚗𝚊𝚝𝚒𝚘𝚗 𝚙𝚊𝚝𝚒𝚎𝚗𝚝𝚜 𝚝𝚑𝚊𝚝 𝚒𝚜 𝚜𝚞𝚙𝚙𝚘𝚜𝚎𝚍 𝚝𝚘 𝚑𝚎𝚕𝚙 𝚝𝚑𝚎 𝚋𝚘𝚍𝚢 𝚊𝚌𝚌𝚎𝚙𝚝 𝚝𝚑𝚎 𝚗𝚎𝚠 𝚘𝚛𝚐𝚊𝚗, 𝚊𝚜 𝚠𝚎𝚕𝚕 𝚊𝚜 𝚊 𝚌𝚑𝚎𝚖𝚘 𝚒𝚗𝚏𝚞𝚜𝚒𝚘𝚗 𝚝𝚑𝚊𝚝 𝙸 𝚠𝚒𝚕𝚕 𝚑𝚊𝚟𝚎 𝚎𝚟𝚎𝚛𝚢 𝚜𝚒𝚡 𝚖𝚘𝚗𝚝𝚑𝚜 𝚒𝚗 𝚛𝚎𝚖𝚒𝚜𝚜𝚒𝚘𝚗 𝚏𝚘𝚛 𝚖𝚊𝚒𝚗𝚝𝚎𝚗𝚊𝚗𝚌𝚎 𝚊𝚗𝚍 𝚖𝚘𝚛𝚎 𝚏𝚛𝚎𝚚𝚞𝚎𝚗𝚝𝚕𝚢 𝚠𝚑𝚎𝚗 𝙸 𝚑𝚊𝚟𝚎 𝚛𝚎𝚕𝚊𝚙𝚜𝚎𝚍. 𝚄𝚗𝚝𝚒𝚕 𝚊 𝚌𝚞𝚛𝚎 𝚒𝚜 𝚏𝚘𝚞𝚗𝚍 𝙸 𝚠𝚒𝚕𝚕 𝚋𝚎 𝚒𝚗 𝚊 𝚌𝚘𝚗𝚜𝚝𝚊𝚗𝚝 𝚌𝚢𝚌𝚕𝚎 𝚘𝚏 𝚛𝚎𝚖𝚒𝚜𝚜𝚒𝚘𝚗 𝚊𝚗𝚍 𝚛𝚎𝚕𝚊𝚙𝚜𝚎. 𝚃𝚑𝚎 𝚛𝚎𝚕𝚊𝚙𝚜𝚎, 𝙸’𝚟𝚎 𝚑𝚎𝚊𝚛𝚍 𝚑𝚊𝚙𝚙𝚎𝚗𝚜 𝚚𝚞𝚒𝚌𝚔𝚕𝚢 𝚊𝚗𝚍 𝚠𝚒𝚝𝚑 𝚕𝚒𝚝𝚝𝚕𝚎 𝚝𝚘 𝚗𝚘 𝚠𝚊𝚛𝚗𝚒𝚗𝚐 𝚜𝚒𝚐𝚗𝚜.𝙸𝚝 𝚑𝚊𝚜 𝚋𝚎𝚎𝚗 𝚟𝚎𝚛𝚢 𝚑𝚊𝚛𝚍 𝚝𝚑𝚒𝚜 𝚙𝚊𝚜𝚝 𝚢𝚎𝚊𝚛 𝚠𝚒𝚝𝚑 𝚝𝚑𝚎 𝚙𝚊𝚗𝚍𝚎𝚖𝚒𝚌 𝚊𝚗𝚍 𝚍𝚎𝚊𝚕𝚒𝚗𝚐 𝚠𝚒𝚝𝚑 𝚝𝚑𝚒𝚜 𝚍𝚒𝚜𝚎𝚊𝚜𝚎. 𝚃𝚑𝚒𝚜 𝚍𝚒𝚜𝚎𝚊𝚜𝚎 𝚑𝚊𝚜 𝚝𝚊𝚔𝚎𝚗 𝚊 𝚝𝚘𝚕𝚕 𝚘𝚗 𝚖𝚢 𝚖𝚎𝚗𝚝𝚊𝚕 𝚑𝚎𝚊𝚕𝚝𝚑 𝚔𝚗𝚘𝚠𝚒𝚗𝚐 𝚝𝚑𝚊𝚝 𝙸 𝚠𝚒𝚕𝚕 𝚑𝚊𝚟𝚎 𝚝𝚑𝚒𝚜 𝚏𝚘𝚛 𝚝𝚑𝚎 𝚛𝚎𝚜𝚝 𝚘𝚏 𝚖𝚢 𝚕𝚒𝚏𝚎 𝚊𝚗𝚍 𝚝𝚑𝚊𝚝 𝚒𝚝 𝚕𝚒𝚖𝚒𝚝𝚜 𝚑𝚘𝚠 𝚖𝚞𝚌𝚑 𝙸 𝚌𝚊𝚗 𝚐𝚘 𝚘𝚞𝚝 𝚒𝚗 𝚙𝚞𝚋𝚕𝚒𝚌, 𝚎𝚜𝚙𝚎𝚌𝚒𝚊𝚕𝚕𝚢 𝚠𝚒𝚝𝚑 𝚝𝚑𝚎 𝚙𝚊𝚗𝚍𝚎𝚖𝚒𝚌. 𝙷𝚊𝚟𝚒𝚗𝚐 𝚖𝚢 𝚒𝚖𝚖𝚞𝚗𝚎 𝚜𝚢𝚜𝚝𝚎𝚖 𝚌𝚘𝚗𝚜𝚝𝚊𝚗𝚝𝚕𝚢 𝚜𝚞𝚙𝚙𝚛𝚎𝚜𝚜𝚎𝚍 𝚖𝚎𝚊𝚗𝚜 𝚝𝚑𝚊𝚝 𝙸 𝚊𝚖 𝚖𝚘𝚛𝚎 𝚜𝚞𝚜𝚌𝚎𝚙𝚝𝚒𝚋𝚕𝚎 𝚝𝚘 𝚐𝚎𝚝𝚝𝚒𝚗𝚐 𝚘𝚝𝚑𝚎𝚛 𝚒𝚕𝚕𝚗𝚎𝚜𝚜𝚎𝚜 𝚊𝚗𝚍 𝙸 𝚊𝚖 𝚗𝚘𝚝 𝚊𝚋𝚕𝚎 𝚝𝚘 𝚏𝚒𝚐𝚑𝚝 𝚝𝚑𝚎𝚖 𝚘𝚏𝚏.𝙸𝚏 𝚢𝚘𝚞 𝚖𝚊𝚍𝚎 𝚒𝚝 𝚝𝚑𝚒𝚜 𝚏𝚊𝚛 𝚘𝚛 𝚊𝚝 𝚝𝚑𝚎 𝚟𝚎𝚛𝚢 𝚕𝚎𝚊𝚜𝚝 𝚌𝚕𝚒𝚌𝚔𝚎𝚍 𝚘𝚗 𝚝𝚑𝚒𝚜 𝚙𝚊𝚐𝚎 𝙸 𝚊𝚖 𝚜𝚘 𝚐𝚛𝚊𝚝𝚎𝚏𝚞𝚕 𝚢𝚘𝚞 𝚝𝚘𝚘𝚔 𝚊𝚗 𝚒𝚗𝚝𝚎𝚛𝚎𝚜𝚝 𝚒𝚗 𝚕𝚎𝚊𝚛𝚗𝚒𝚗𝚐 𝚊𝚋𝚘𝚞𝚝 𝚖𝚢 𝚍𝚒𝚜𝚎𝚊𝚜𝚎. 𝙸 𝚊𝚖 𝚐𝚛𝚊𝚝𝚎𝚏𝚞𝚕 𝚏𝚘𝚛 𝚊𝚕𝚕 𝚝𝚑𝚎 𝚐𝚘𝚘𝚍 𝚒𝚗𝚝𝚎𝚛𝚊𝚌𝚝𝚒𝚘𝚗𝚜 𝙸 𝚑𝚊𝚟𝚎 𝚑𝚊𝚍 𝚘𝚗 𝚖𝚢 𝚜𝚘𝚌𝚒𝚊𝚕 𝚖𝚎𝚍𝚒𝚊𝚜 𝚊𝚗𝚍 𝚝𝚑𝚎 𝚖𝚞𝚝𝚞𝚊𝚕𝚜 𝙸 𝚑𝚊𝚟𝚎 𝚖𝚊𝚍𝚎 𝚝𝚑𝚊𝚝 𝚖𝚊𝚔𝚎 𝚖𝚢 𝚍𝚊𝚢 𝚜𝚘 𝚖𝚞𝚌𝚑 𝚋𝚎𝚝𝚝𝚎𝚛. 𝚃𝚑𝚊𝚗𝚔 𝚢𝚘𝚞 𝚜𝚘 𝚖𝚞𝚌𝚑 𝚏𝚘𝚛 𝚛𝚎𝚊𝚍𝚒𝚗𝚐 𝚊𝚗𝚍 𝙸 𝚕𝚘𝚟𝚎 𝚢𝚘𝚞.