@asiertombangi: #cejour-là

Asierto Mbangi
Asierto Mbangi
Open In TikTok:
Region: CD
Sunday 30 August 2026 17:35:08 GMT
1838
158
6
5

Music

Download

Comments

www.tikkongo
Zaïre :
Oyo masumu bozo salisa biso mabe te?
2026-08-30 19:04:19
0
louis.segond.kamb
Louis segond Kambale :
c'est pas en dire que Dieu ne savait pas qu' Adam et Eve avaient déjà pêchés , seulement en posant la question il voulait stimuler le cœur d'Adam
2026-08-30 19:29:02
0
lg_boss
Gloire Luzolo :
eloko wana nga pe elekelaka nga fort
2026-08-30 18:51:56
1
albertoalambuni
albertoalambuni :
Dieu aussi ne voyais pas là où ils ont été caché
2026-08-30 18:19:38
0
cestbigflex
bigflex_officiel :
🙏🙏🙏🙏
2026-08-30 18:09:01
1
miradie0000
Miradie❣️💔♥️ :
❤️❤️❤️
2026-08-30 17:43:14
0
To see more videos from user @asiertombangi, please go to the Tikwm homepage.

Other Videos

Halo was born with an extremely rare genetic disorder called CTBP1-related disorder, something that affects her development, muscle tone, and ability to manage many things that most children can do instinctively. She was admitted to Albany Medical Center after becoming sick with rhinovirus and aspiration pneumonia. Because of her low muscle tone, she struggled to clear her own airways, and what started as an infection eventually progressed into hypoxic respiratory failure. Last Tuesday, everything changed. Halo’s oxygen saturation suddenly dropped, and she coded. Watching the medical team work to bring my daughter back is something I will carry with me for the rest of my life. That same day, we had a conversation no parent should ever have to sit through. We talked about her prognosis, her future, and what her life could look like if she continued to deteriorate. I never imagined I would be sitting beside my daughter having a conversation about how much time she might have left. That day, I asked for Halo to be baptized. In the middle of the fear and uncertainty, I wanted to give her to God, pray over her, and give her the blessing of salvation. And somehow, since that day, Halo has continued to fight. She has made progress. She has surprised us. She has shown me, over and over again, that she isn’t finished fighting yet. I don’t know what tomorrow holds. I don’t know how this story ends. But today, she’s here. She’s in my arms, just like the very first time I held her.  And for today, that’s enough. 🤍 #fyp #fypシ #foryoupage #viral #support
Halo was born with an extremely rare genetic disorder called CTBP1-related disorder, something that affects her development, muscle tone, and ability to manage many things that most children can do instinctively. She was admitted to Albany Medical Center after becoming sick with rhinovirus and aspiration pneumonia. Because of her low muscle tone, she struggled to clear her own airways, and what started as an infection eventually progressed into hypoxic respiratory failure. Last Tuesday, everything changed. Halo’s oxygen saturation suddenly dropped, and she coded. Watching the medical team work to bring my daughter back is something I will carry with me for the rest of my life. That same day, we had a conversation no parent should ever have to sit through. We talked about her prognosis, her future, and what her life could look like if she continued to deteriorate. I never imagined I would be sitting beside my daughter having a conversation about how much time she might have left. That day, I asked for Halo to be baptized. In the middle of the fear and uncertainty, I wanted to give her to God, pray over her, and give her the blessing of salvation. And somehow, since that day, Halo has continued to fight. She has made progress. She has surprised us. She has shown me, over and over again, that she isn’t finished fighting yet. I don’t know what tomorrow holds. I don’t know how this story ends. But today, she’s here. She’s in my arms, just like the very first time I held her. And for today, that’s enough. 🤍 #fyp #fypシ #foryoupage #viral #support

About