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JustJordan33

I'm Jordan Mae! I am a 21 year old BYU college student from Utah creating a video diary of my daily life. I love challenges, food, school, makeup, hair, travel, life hacks, hiking, adventures, and honestly just having fun. SUBSCRIBE so we can stay in touch! New videos every Saturday :D Check out my website: https://justjordan33.fun/
  • 2.1M subscribers,
  • 793 videos
Views/7days31,352
Like/Views3.5%
Last Updated3 days ago

AllAroundAudrey

Audrey has a fun, creative, and energetic personality that radiates through her videos. She covers video genres such as challenges, games, adventures, vlogs, and reviews. Audrey loves to film fun videos that captivates her audience to come along for the journey! Audrey recently got married, and her and her husband are excited for their audience to come along their journey as they share what their life is like as new homeowners and travel enthusiasts! My Other Channels: Aud Vlogs: https://www.youtube.com/@audvlogs Audrey and Spencer: https://www.youtube.com/@audreyandspencer Social Media: Instagram- https://instagram.com/allaroundaudrey/ Facebook- https://www.facebook.com/AllAroundAudrey?ref=profile TikTok- AllAroundAudrey
  • 1.9M subscribers,
  • 1.1K videos
Views/7days21,418
Like/Views3.1%
Last Updated3 days ago

Jordan Mae

  • 370K subscribers,
  • 122 videos
Like/Views3.4%
Last Updated2 years ago

Gundy Bear

  • 1.3K subscribers,
  • 0 videos

The Auspicious Family

We are the Auspicious Family. Our journey is all about overcoming hardships. You see our oldest son Noah is on the autism spectrum and for 12 yrs we overcame all the difficulties that our son had to face, My wife and i decided to give him a sibling that can look after him, as we get older. We didn't want him to be alone, Enter Nathan our 2 yr old baby boy. We were so excited, a new member of the family but sadly things don't always go as we plan, Our baby was born with a rare genetic disease that affects less than 1 in a million kids. Few cases known worldwide. He suffers from seizures, severe reflux and vomiting, cataracts, loose skin, hernias, trouble feeding, small limbs and developmental delays, in other words he needs full time care. We stopped working and decided to document our journey, parenting autism and Cutis Laxa. We ask everyone to please help us share our story, in hopes that someone out there can help our son Nathan with this rare disease.
  • 9.4K subscribers,
  • 0 videos