@the25comfit: Try do it #CapCut #xh #fyp #Fitness #tapgymmoingay #bodycare #foryou

25 COMFIT

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Friday 03 May 2024 13:58:25 GMT

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April 🦋 :

Đẹp 😍

2024-05-04 05:31:58

3

Mộc 🤡 :

Đẹp quá ám ảnh mất🥰🥰

2024-05-22 11:51:48

1

Minh An :

💪💪💪

2024-05-03 14:50:35

1

ຮ້ານຂາຍເສື້ອຜ້າ P&S ຍິງ_ຊາຍ :

🥰

2024-06-28 01:39:02

0

Lan Anh_nè :

Mê 🥰

2024-05-07 18:23:05

0

Sunshine’s :

Mêeeeeeee

2024-05-06 09:01:11

0

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Sorry to burst your bubble, but this isn’t a seasonal cold — it’s forever sick. You don’t have to tilt your head and whisper, “I just can’t imagine how hard that must be…” Babes, let me tellllll you. I’ve lived it. Sobbed through it. And then still found myself — and joy, and purpose — through it. And dark humor… obviously. Being chronically ill doesn’t mean my life is miserable. It just means my baggage showed up early, uninvited, and invisible to most. And yeah, sometimes it’s heavy. Sometimes it sucks. But not every day is tragic. Not every day needs soft lighting and sad piano music. I have good days and bad days — just like everyone else. That’s called life. The important caveats? My good days sometimes feel capped — both in what I can do, and how many days like that I get. But I make them count. I really, really do. And my bad days? Well they are REALLY f*cking bad. Some of them have absolutely gutted me. And yet I somehow survived them all. So no, I’m not “sick” like cold sick. I’m sick like chronic, complicated, resilient, sarcastic sick. And I promise — you don’t have to feel uncomfy about it. I’m certainly not. So to my sick friends, what’s one thing you wish healthy people really understood about chronic illness life? And my brave healthy friends, what’s one thing you’ve always quietly wondered about my life with chronic illness? #chronicillnesscommunity #autoimmunewarrior #spooniesupport #invisibleillnessawareness #chronicpainwarrior #invisibledisability #fyp #creatorsearchinsights

Sorry to burst your bubble, but this isn’t a seasonal cold — it’s forever sick. You don’t have to tilt your head and whisper, “I just can’t imagine how hard that must be…” Babes, let me tellllll you. I’ve lived it. Sobbed through it. And then still found myself — and joy, and purpose — through it. And dark humor… obviously. Being chronically ill doesn’t mean my life is miserable. It just means my baggage showed up early, uninvited, and invisible to most. And yeah, sometimes it’s heavy. Sometimes it sucks. But not every day is tragic. Not every day needs soft lighting and sad piano music. I have good days and bad days — just like everyone else. That’s called life. The important caveats? My good days sometimes feel capped — both in what I can do, and how many days like that I get. But I make them count. I really, really do. And my bad days? Well they are REALLY f*cking bad. Some of them have absolutely gutted me. And yet I somehow survived them all. So no, I’m not “sick” like cold sick. I’m sick like chronic, complicated, resilient, sarcastic sick. And I promise — you don’t have to feel uncomfy about it. I’m certainly not. So to my sick friends, what’s one thing you wish healthy people really understood about chronic illness life? And my brave healthy friends, what’s one thing you’ve always quietly wondered about my life with chronic illness? #chronicillnesscommunity #autoimmunewarrior #spooniesupport #invisibleillnessawareness #chronicpainwarrior #invisibledisability #fyp #creatorsearchinsights

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