@hatim_vibes_2: #wutheringwaves #wuwacreator I keep thinking about how this kind of technology could actually be introduced. I thought it was so cool to see people generating energy just from walking and using it to power traffic lights or displays. What do you think about this technology? FreeFire #BooyahMerdeka#FreeFire #Booyah Merdeka #PUBGMBrainrot #ببجی #PUBGMWOW450#tiktokminsgame #game Did you know? #girlsgame#MarvelRivals #บรีสเอกเซล #freefire_lover #ท้ายexcel #ไฮไลท์ฟี Fire in #garenarov #rov #wibgajian #荒野行動 # 荒野 #荒野女子 #njoy #スマブラ #sp #理下 #対複 #wilderness #荒野行動儿#荒野男子 #荒野行動工šk #war #gyat #reddittiktok #cs2 #mw3 #highlights #redditstoriestts #mortalkombat #fc24 #zepetoapp #monkey #adventuretime #mk1 #totaldrama #freefire #spiderman2 #mortalkombat1 #npc #hololive #gamesnotiktok #otaku #a #japanese #travel #stitch #mexico #kyoto #japantravel #wtfmoments #fncs #totaldramaisland #cosplays #manotouhinhh #hantohiinin #anime #animeedit #animeedits #animeclips #animefyp #animefan #animefans #animecommunity #manga #narutouzumaki #sasuke #kakashi #boruto #onepiece #luffy #zoro #sanji #nami #gear5 #naruto #jujutsukaisen #jjk #gojo #gojosatoru #itadori #sukuna #demonslayer #kimetsunoyaiba #tanjiro #nezuko #zenitsu #AttackOnTitan #aot #levi #erenyeager #mikasa #spyxfamily #anya #anyaforger #dragonball #dragonballz #goku #vegeta #chainsawman #denji #makima #bluelock #isagi #bachira #haikyuu #hinata #kageyama #tokyorevengers #mikey #draken #hunterxhunter #gon #killua #sololeveling #sungjinwoo #pokemon #pikachu #pokemonanime #GenshinImpact #genshin #hoyoverse #HonkaiStarRail #hsr #zenlesszonezero #zzz #bluearchive #nikke #nikkegoddessofvictory #umamusume #pokemongo #dragonballlegends #projectsekai #fategrandorder #arknights #azurlane #mobilelegends #mlbb #honorofkings #hok #leagueoflegends #wildrift _It's installed in places where countless commuters pass by and is used to power LED lighting or displays. I think this is a great way to build a sustainable society and smart cities. What do you all think about this technology? What do you think about this technology? In Japan, piezoelectric tiles (piezoelectric tiles) are used to turn the power of people's footsteps and walking into electricity. The energy generated by millions of commuters every day is harnessed to power LED lights and displays in crowded places like Shibuya Station. It's a great technique for # Njoy umamusume pokemongo dragonballlegends projectsekai fategrandorder arknights azurlane mobilelegends mlbb honorofkings hok leagueoflegends wildrift pubgmobile The freefire Valorant Minecraft roblox gaming gamer mobilegaming gameplay gamingclips gamingvideo gamingcommunity esports proplayer ranked viral fyp foryou foryoupage trend trending viralvideo tiktokviral animegaming animegirl animeboy animeart animeworld animejapan japananime japan tokyo akihabara nihon šk tiktok

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I saw a comment today that honestly stopped me in my tracks. A mother was sharing the life of her daughter, a little girl with significant disabilities who relies on medical equipment. Someone decided to declare that this child has a “miserable life,” referred to her as a “meat puppet,” and accused her mother of keeping her alive and using her daughter merely for content. Let that sink in. As a mother of a child with Down syndrome, I can tell you how incredibly wrong that perspective can be. Parents of children with disabilities don't share our lives online because we think our children are content. We share because visibility matters. We share because there are people who have never spent time with someone who has a disability. People who have never seen the appointments, the therapies, the victories, the frustrations, the belly laughs, the stubbornness, the personality, the milestones that may look different but are celebrated just as fiercely sometimes even more so because the journey to achieve that milestone was much longer. We share so you can SEE the child instead of seeing a diagnosis. We share so you can learn that a child who communicates differently still has something to say. That a child who moves differently still wants to play. That a child who learns differently is still learning. That a child who needs medical equipment is still a CHILD. And yes, sometimes we share the hard stuff, too. Because disability isn't a carefully edited highlight reel. There are difficult days. There are scary moments. There are things our children have to work harder to accomplish than other children. But difficult does not automatically mean miserable. Different does not mean less. Needing medical support does not mean a life isn't worth living. And a parent choosing to share their child's journey does not mean they are exploiting their child. For many of us, we're trying to change the world our children are growing up in. We're trying to replace fear with understanding. Pity with acceptance. Ignorance with education. And stereotypes with an actual human face. My son has Down syndrome. He is not a diagnosis walking around in a little body. He's a little boy with a personality, preferences, opinions, humor, frustrations, joys and an entire life ahead of him. And I want people to know him. I want people to see him. I want people to understand that children with disabilities aren't here merely to be cared for. They are here to live, learn, love, laugh, experience, grow and participate in this world right alongside everyone else. That's why we share. Not because our children are content. Because our children deserve to be seen. #downsyndromeawareness  #Declan  #fypシ
I saw a comment today that honestly stopped me in my tracks. A mother was sharing the life of her daughter, a little girl with significant disabilities who relies on medical equipment. Someone decided to declare that this child has a “miserable life,” referred to her as a “meat puppet,” and accused her mother of keeping her alive and using her daughter merely for content. Let that sink in. As a mother of a child with Down syndrome, I can tell you how incredibly wrong that perspective can be. Parents of children with disabilities don't share our lives online because we think our children are content. We share because visibility matters. We share because there are people who have never spent time with someone who has a disability. People who have never seen the appointments, the therapies, the victories, the frustrations, the belly laughs, the stubbornness, the personality, the milestones that may look different but are celebrated just as fiercely sometimes even more so because the journey to achieve that milestone was much longer. We share so you can SEE the child instead of seeing a diagnosis. We share so you can learn that a child who communicates differently still has something to say. That a child who moves differently still wants to play. That a child who learns differently is still learning. That a child who needs medical equipment is still a CHILD. And yes, sometimes we share the hard stuff, too. Because disability isn't a carefully edited highlight reel. There are difficult days. There are scary moments. There are things our children have to work harder to accomplish than other children. But difficult does not automatically mean miserable. Different does not mean less. Needing medical support does not mean a life isn't worth living. And a parent choosing to share their child's journey does not mean they are exploiting their child. For many of us, we're trying to change the world our children are growing up in. We're trying to replace fear with understanding. Pity with acceptance. Ignorance with education. And stereotypes with an actual human face. My son has Down syndrome. He is not a diagnosis walking around in a little body. He's a little boy with a personality, preferences, opinions, humor, frustrations, joys and an entire life ahead of him. And I want people to know him. I want people to see him. I want people to understand that children with disabilities aren't here merely to be cared for. They are here to live, learn, love, laugh, experience, grow and participate in this world right alongside everyone else. That's why we share. Not because our children are content. Because our children deserve to be seen. #downsyndromeawareness #Declan #fypシ

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