@skynewsarabia: "فتيان التلال".. من هم أخطر جماعة استيطانية في الضفة الغربية؟ #سوشال_بالتفصيل

SkyNewsArabia
SkyNewsArabia
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Region: AE
Monday 27 July 2026 19:30:00 GMT
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user618763939431
قمر الدين :
حسبنا الله ونعم الوكيل فيهم
2026-07-28 12:31:36
0
1.1518
الحمدلله دائما وابدا :
اللهم أنصر أهل فلسطين يارب العالمين
2026-07-28 10:00:34
0
user3669422612932
ماجد الحربي :
2026-07-28 01:27:00
0
satan9540
satan :
ليش ما إسمهم الإرهابيون ، لو كانوا عرب بدولة عربية يحملون السلاح ظد يهود كانوا إرهابييون و دول العربية هي لتسجنهم
2026-07-28 14:55:14
0
al_lail_
الليل 🇸🇦 :
ياخي ما فيهم رحمه ولا انسانيه .. كيف تستولي على بيت ماهو بيتك ولا تحترم مسن ولا طفل ولا امراءه.. متى تنقلب الادوار
2026-07-27 19:35:49
0
y.asser0
ياسر :
2026-07-27 21:26:27
1
user30251124515161
بسام طالب :
😞😞😞
2026-07-27 19:43:59
0
nozad773
NOZAD :
🥰🥰🥰
2026-07-28 06:07:00
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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