@jenniifor: If you are in Marrakech you have to visit this restaurant. #maroc #marrakech #marokko #marrakesh #morocco #fy #foryoupage #fyp #restaurant #greek #foodspot #restaurante #food #vacation

Jennifer
Jennifer
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Region: NL
Sunday 26 May 2024 19:39:47 GMT
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chamaamed0
🖤 :
Les prix 🙄
2024-06-16 00:59:52
1
achfrguu
A’ :
Can I know his name?
2024-06-22 01:51:44
2
lavieestbelle172
🎀Jojo🎀🥀 :
Où exactement
2024-06-16 21:48:41
1
no_one1xx
no_one1xx :
So good🥰
2024-06-28 13:27:29
1
maryamrim49
rim :
Safran hsn mni
2025-05-16 19:11:32
0
jjpau64110
JJpau64110 :
j'ai regardé le menu c'est très cher
2024-08-05 18:49:40
0
topquad.marrakech
TOP QUAD MARRAKECH :
amazing
2024-06-14 21:57:13
1
hsseinejray
🕊 :
my fav✨
2024-06-16 13:20:07
2
rhitaatl
rhitaatl :
@Sam.mus
2024-06-21 10:17:34
2
red_city_concierge
red_city_concierge :
🥰🥰🥰
2024-06-25 15:17:19
1
1bzzz
1bz :
💙
2024-06-20 15:07:15
1
the_mounlight
zerhouni mounia :
🥺🥺🥺
2025-06-08 15:26:31
0
khadija.arsalan4
Khadija Arsalan :
👑
2025-03-23 04:30:40
0
alhoceima01
Alhoceima❤️ :
🥰🥰🥰
2025-02-19 20:24:26
0
rmysgr_c
rmysgr_c :
Location de voiture @Sgrccar_kech les besttt💥
2024-08-03 14:46:20
0
amounib95
Imane amoouni :
@Leila jamal
2024-07-07 22:24:41
0
casaboss5
Samir 🇲🇦 🇩🇿 :
Pue la merde le restaurant à fuir
2024-05-28 03:13:45
3
fafa_wawa7
Fluffy :
@dunia_rguig Hadi mchat liha lbnt li la jibi mn endha les cmnd waeraaaaaaaaa
2025-02-18 18:04:04
1
z.fati
Z.Fati 🇲🇦 :
Mais makla la3alak haltha plus prix mayasthlch
2024-06-26 10:30:36
1
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Other Videos

Tonight shook me to my core. I came to the hospital because I was in unbearable pain. My body felt like it was shutting down. My bloodwork was abnormal. I could barely function. I knew something was seriously wrong. They told me it’d be hours. So I went home, even though I was in agony. Eventually, I couldn’t take it anymore. I called the ambulance because I was scared — terrified — and the pain was too much. They brought me back to emergency… and instead of being treated urgently, they wheeled me into a chair… and left me in the waiting room. I was sobbing. In front of everyone. Crying in pain, shaking, barely hanging on. And no one came. No nurse. No doctor. Just people walking past me like I didn’t exist. And I hate to say it, but I truly believe if I wasn’t Indigenous, I would’ve been treated differently. I’ve felt this kind of dismissal before — and it cuts deep. After hours of crying and waiting, they finally brought me into a room. They looked at my abnormal bloodwork… And told me it was probably “just constipation.” Just. Constipation. Like the level of pain I was in didn’t matter. Like the fact that I could barely walk didn’t matter. Like my tears, my panic, my entire body screaming — was an exaggeration. They told me to just take my pain meds and wait for the doctor. No urgency. No real explanation. No care. And I’m still here. Still in pain. Still waiting. Still crying. The physical pain is unbearable — but honestly, the emotional pain? Of being ignored, dismissed, dehumanized? It’s worse. I didn’t come in for attention. I came in because I was scared. I’m fighting a body that constantly turns against me — and now I have to fight to be believed too? I deserve better. We all do. To every Indigenous person, every chronically ill person, every woman who’s been told “it’s nothing” — I see you. You are not alone. And you deserve to be treated like your pain matters. #IndigenousRights #MedicalNeglect #SystemicRacism #InvisibleIllness #AutoimmuneWarrior #ChronicPain #HospitalTrauma #BelievePatients #IndigenousAndStrong #YouAreNotAlone #AutoimmuneLife #YouAreNotAlone #FightingSilently #autoimmunediseasewarrior #chronicillness #chronicpainwarrior #crpswarrior #crpsawareness #ChronicPainLife #FlareDay #autoimmunemom #potsawareness #momswithchronicillness #chronicillness #trigeminalneuralgia #trigeminalneuralgiaawareness #crpsawareness #crpswarrior #dysautonomiapots #MysteryIllness #SpoonieSupport #chronicregionalpainsyndrome #relatable #relatablepost #readthecaption
Tonight shook me to my core. I came to the hospital because I was in unbearable pain. My body felt like it was shutting down. My bloodwork was abnormal. I could barely function. I knew something was seriously wrong. They told me it’d be hours. So I went home, even though I was in agony. Eventually, I couldn’t take it anymore. I called the ambulance because I was scared — terrified — and the pain was too much. They brought me back to emergency… and instead of being treated urgently, they wheeled me into a chair… and left me in the waiting room. I was sobbing. In front of everyone. Crying in pain, shaking, barely hanging on. And no one came. No nurse. No doctor. Just people walking past me like I didn’t exist. And I hate to say it, but I truly believe if I wasn’t Indigenous, I would’ve been treated differently. I’ve felt this kind of dismissal before — and it cuts deep. After hours of crying and waiting, they finally brought me into a room. They looked at my abnormal bloodwork… And told me it was probably “just constipation.” Just. Constipation. Like the level of pain I was in didn’t matter. Like the fact that I could barely walk didn’t matter. Like my tears, my panic, my entire body screaming — was an exaggeration. They told me to just take my pain meds and wait for the doctor. No urgency. No real explanation. No care. And I’m still here. Still in pain. Still waiting. Still crying. The physical pain is unbearable — but honestly, the emotional pain? Of being ignored, dismissed, dehumanized? It’s worse. I didn’t come in for attention. I came in because I was scared. I’m fighting a body that constantly turns against me — and now I have to fight to be believed too? I deserve better. We all do. To every Indigenous person, every chronically ill person, every woman who’s been told “it’s nothing” — I see you. You are not alone. And you deserve to be treated like your pain matters. #IndigenousRights #MedicalNeglect #SystemicRacism #InvisibleIllness #AutoimmuneWarrior #ChronicPain #HospitalTrauma #BelievePatients #IndigenousAndStrong #YouAreNotAlone #AutoimmuneLife #YouAreNotAlone #FightingSilently #autoimmunediseasewarrior #chronicillness #chronicpainwarrior #crpswarrior #crpsawareness #ChronicPainLife #FlareDay #autoimmunemom #potsawareness #momswithchronicillness #chronicillness #trigeminalneuralgia #trigeminalneuralgiaawareness #crpsawareness #crpswarrior #dysautonomiapots #MysteryIllness #SpoonieSupport #chronicregionalpainsyndrome #relatable #relatablepost #readthecaption

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