@usser.rt: #pov #fyp

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Region: FR
Monday 18 May 2026 09:37:05 GMT
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canela_13..1
Solycanela 🇩🇴 :
On est si jeune et détruit mentalement 🫩
2026-05-18 18:58:28
11
roxaneyao64
. :
Tellement envie de revenir en arrière 💔
2026-07-16 19:43:09
0
maxlamenace_3
MaxLaMenace :
depuis peu j’ai pu comprendre une chose c’est que dans la vie, la seule chose dont nous avons besoin c’est de faire la paix intérieure avec soi même pour retrouver sa force, sa personnalité et sa clarté pour mieux avancer
2026-05-23 18:40:56
4
ins.dabir0
Inès Dabiré :
xva allez dieu est grand
2026-07-20 15:42:30
0
wilfried1567
wilfried🪬♣️ :
depuis l'âge de 15 ans je comprends plus ma life 🥺💔
2026-07-20 02:23:34
0
.adjaa01
.adjaa01 :
Bahh oui 😭😮‍💨😔
2026-05-30 03:48:50
0
user909017202
… :
J’aimerais tellement redevenir la petite fille d’avant qui était juste joyeuse , au lieu d’être une grande fille détruite et malheureuse 😔
2026-06-04 09:39:57
0
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I’m in constant pain and raising funds for the corrective surgery that will finally let me breathe, eat, and live more comfortably. ✨ Anything helps — like, share, comment, follow, or donate. Every bit gets me closer to a life without constant pain. My GoFundMe is linked in my profile. Thank you for being here 💛 💛 In 2020, my jaw locked shut. Multiple specialists gave me mixed advice — some did procedures, some said it was all in my head, and the military didn’t know what was happening either. I was paying out-of-pocket, but the pain only got worse. In 2022, I finally found a TMJ specialist who discovered a tumor and recommended surgery to remove extra bone, bring my jaw forward, open my airway, and place prosthetics properly — but I couldn’t afford it. In 2023, the military removed the tumor and put in prosthetics… but didn’t fix the extra bone or bring my jaw forward. My airway is still narrow, my jaw is painful to move, and everyday tasks are a struggle. It wasn’t until 2025, when I returned to the specialist, that I was diagnosed with EDS (Ehlers-Danlos Syndrome) — a connective tissue disorder that caused my joints, including my jaw, to be hypermobile and unstable. Now in 2026, I’m still in pain and raising funds for the corrective surgery that will finally let me breathe, eat, and live more comfortably. ✨ Anything helps — like, share, comment, follow, or donate. Every bit gets me closer to a life without constant pain. My GoFundMe is linked in my profile. Thank you for being here 💛 #chronicpain #chronicillness #pots #eds #pcos
I’m in constant pain and raising funds for the corrective surgery that will finally let me breathe, eat, and live more comfortably. ✨ Anything helps — like, share, comment, follow, or donate. Every bit gets me closer to a life without constant pain. My GoFundMe is linked in my profile. Thank you for being here 💛 💛 In 2020, my jaw locked shut. Multiple specialists gave me mixed advice — some did procedures, some said it was all in my head, and the military didn’t know what was happening either. I was paying out-of-pocket, but the pain only got worse. In 2022, I finally found a TMJ specialist who discovered a tumor and recommended surgery to remove extra bone, bring my jaw forward, open my airway, and place prosthetics properly — but I couldn’t afford it. In 2023, the military removed the tumor and put in prosthetics… but didn’t fix the extra bone or bring my jaw forward. My airway is still narrow, my jaw is painful to move, and everyday tasks are a struggle. It wasn’t until 2025, when I returned to the specialist, that I was diagnosed with EDS (Ehlers-Danlos Syndrome) — a connective tissue disorder that caused my joints, including my jaw, to be hypermobile and unstable. Now in 2026, I’m still in pain and raising funds for the corrective surgery that will finally let me breathe, eat, and live more comfortably. ✨ Anything helps — like, share, comment, follow, or donate. Every bit gets me closer to a life without constant pain. My GoFundMe is linked in my profile. Thank you for being here 💛 #chronicpain #chronicillness #pots #eds #pcos

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