@nguwarnaing1:

ထားထက်ထက် မေမေ ( Triple H )❤️
ထားထက်ထက် မေမေ ( Triple H )❤️
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Region: MM
Thursday 20 August 2026 04:26:10 GMT
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.ba.gay
U Naing :
အမရယ်🥺
2026-08-20 15:12:15
0
aung.pyae.phyo46
🖤🇲🇲လူကြမ်းကြီး ဒဿ🇨🇳🖤✡ :
သနပ်ခါးကုန်ရင်ပြောပါဗျ အမြဲတမ်းတင်ပေးပါ
2026-08-30 09:15:31
1
nay.htet.lin8691
Nay Htet Lin.NhL :
မေမေလေးရာ အရမ်းကိုချစ်စယာလေးပါ လူကလည်းချော ချစ်စယာလေးလဲအရမ်းကောင်း မျတ်နှာကျလေးလည်းအကြည်ဓာတ်လေး နှုတ်ခမ်းသားဖူးဖူးလေးနဲ့ တကယ့်ကိုဆွဲဆောင်မှုခပ်ပြင်းပြင်းလေးနဲ့ကိုလှနေတာပါ🥰
2026-08-29 01:51:19
1
komaung673
Min Khant :
မမ လှလိုက်တာ
2026-09-07 05:21:44
0
rin713422
Rin :
ချစ်စရာလေးထားရယ်❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️
2026-09-08 07:08:22
0
user6503448575486
my love :
သခုသခုမြရတယ်
2026-09-06 16:15:06
0
ye.thway566
ချစ်မ၀လေးရဲ့ကိုကို :
မိုက်ကြိကြိသနပ်ခါးက
2026-08-30 12:18:57
0
antymathin
မေမေ :
၁တုံးဘယ်လေက်လဲသနပ်ခါး
2026-08-20 05:03:01
1
aung.zaw6876
Aung Zaw :
မဂ်လာနံနက်ခင်းပါ
2026-10-06 03:19:14
0
aung.sit.thi.aung
Aung sit thi Aung sit thi :
အယ်ယ်ယ်ယ်................🥰😘
2026-08-29 16:21:03
0
kotharlay1
seven,,day :
လှလိုက်တဲ့ဆွဲကြိုး😁
2026-09-03 14:39:12
0
ye.htut.aung598
🫣ချစ်သူနဲ့ဝေး🥰 :
ဂေါ်ထွတ်နေတာပဲ
2026-08-31 13:10:07
0
c.t.aung44
🇲🇲🇲🇲C T AUNG🇲🇲🇲🇲 :
တတ်တူးဘယ်နဲ့ကွတ်လဲ့😎😎
2026-09-06 12:11:45
0
aalpn21
Steven :
2026-09-05 23:25:02
0
zarni3432
zarni :
2026-08-29 14:43:40
0
zeno23456789999998889999
đĝéÿ :
2026-09-07 15:00:55
0
lin33gyi
Pauck Thee၊ :
😍😍😍
2026-08-28 13:00:21
0
phyolay1500150015
Phyo Lay :
😳
2026-08-22 05:58:24
0
than.win.soe098
Than :
ချစ်တယ့်ကွာ🥰🥰🥰🥰🥰🥰🥰🥰🥰🥰🥰
2026-08-21 08:43:16
0
myothu6561
Ma Ma :
မမ
2026-08-28 09:12:11
0
user2j2qpdqu2u
I Like This🍑 :
ကြည့်မဝဘူး 🥰 @theguyslike 🥰
2026-10-06 12:18:57
0
myoq31
💞💞💞Anyar Thar💞💞💞 :
2026-08-28 04:10:07
0
saw.phoe.khwar830
Saw Phoe Khwar :
သနပ်ခါးတလုံးဘယ်လိုရောင်းလည်း
2026-08-25 18:01:33
0
sai.minkhant51
Sai往事的飞花 辞九门回忆.chefCooking🇲🇲 :
2026-08-20 20:30:04
0
To see more videos from user @nguwarnaing1, please go to the Tikwm homepage.

Other Videos

💛 Endometriosis Awareness Month 💛 I was around 15 when the pain started, I’m 31 now. For years I was told it was ‘normal’, ‘just bad periods’, ‘anxiety’ or my favourite ‘all in my head’.  In 2018, a GP looked me in the face and told me it was impossible for me to have endometriosis. It was later that night I was diagnosed with Endometriosis via ultrasound (which is very rare and not the norm) in the emergency department.  Since then…  • Had 4 laparoscopies for endo, 1 ablation and 3 excision.  • Had bowel and kidney involvement • My left ovary removed • Both fallopian tubes removed • Frozen my eggs • Spent 9 months in chemically induced menopause via a cancer drug • More hospital admissions than I can count And I didn’t just “try the pill.” I’ve also tried hormonal pills, multiple medications, antidepressants for nerve pain, nerve blocks, pelvic floor Botox, ketamine infusions, nerve medications, pain specialists and a million more things. You name it, I’ve tried it. When you’re in debilitating pain every day you’ll try anything to get your life back. The hardest part wasn’t just the physical pain. It was the grief, the emotional toll this all takes, the fear I’ll never be a mother, the medical gaslighting and the constant advocating I’ve had to do to prove I was sick enough to deserve help.  Endometriosis is not just bad periods, it’s a complex full body inflammatory disease. It can affect organs far beyond the uterus and has been found on every single organ in the body including the lungs, kidney, skin and even the brain.  If there’s one thing I’ve learnt throughout this journey it’s YOU KNOW YOUR BODY BEST!!!!! Trust your gut and if something doesn’t feel right keep going. Seek another opinion, find a doctor who listens and one that respects your wishes. Do not shrink yourself to make someone else comfortable (doctor or not).  Being heard changes lives and earlier diagnosis changes lives. Remember, are never too young to have endometriosis. And to every person navigating this disease, I see you and know I will always continue to fight for us all 💛 #endometriosis #endoawarenessmonth #endo #endometriosisawareness #endometriosissupport
💛 Endometriosis Awareness Month 💛 I was around 15 when the pain started, I’m 31 now. For years I was told it was ‘normal’, ‘just bad periods’, ‘anxiety’ or my favourite ‘all in my head’. In 2018, a GP looked me in the face and told me it was impossible for me to have endometriosis. It was later that night I was diagnosed with Endometriosis via ultrasound (which is very rare and not the norm) in the emergency department. Since then… • Had 4 laparoscopies for endo, 1 ablation and 3 excision. • Had bowel and kidney involvement • My left ovary removed • Both fallopian tubes removed • Frozen my eggs • Spent 9 months in chemically induced menopause via a cancer drug • More hospital admissions than I can count And I didn’t just “try the pill.” I’ve also tried hormonal pills, multiple medications, antidepressants for nerve pain, nerve blocks, pelvic floor Botox, ketamine infusions, nerve medications, pain specialists and a million more things. You name it, I’ve tried it. When you’re in debilitating pain every day you’ll try anything to get your life back. The hardest part wasn’t just the physical pain. It was the grief, the emotional toll this all takes, the fear I’ll never be a mother, the medical gaslighting and the constant advocating I’ve had to do to prove I was sick enough to deserve help. Endometriosis is not just bad periods, it’s a complex full body inflammatory disease. It can affect organs far beyond the uterus and has been found on every single organ in the body including the lungs, kidney, skin and even the brain. If there’s one thing I’ve learnt throughout this journey it’s YOU KNOW YOUR BODY BEST!!!!! Trust your gut and if something doesn’t feel right keep going. Seek another opinion, find a doctor who listens and one that respects your wishes. Do not shrink yourself to make someone else comfortable (doctor or not). Being heard changes lives and earlier diagnosis changes lives. Remember, are never too young to have endometriosis. And to every person navigating this disease, I see you and know I will always continue to fight for us all 💛 #endometriosis #endoawarenessmonth #endo #endometriosisawareness #endometriosissupport

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