Born This Way: Moving Forward – Original Casting Footage (Digital Exclusive) | A&E

Don’t miss “A Very Born This Way Christmas,” the Born This Way series finale Christmas special, airing 12/18 at 9pm ET/PT only on A&E.

In episode 5 of the digital series, “Born This Way: Moving Forward,” original audition footage is shared and the showrunners discuss their casting process. #BornThisWay
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“Born This Way” follows a group of seven young adults born with Down syndrome as they pursue their passions and lifelong dreams, explore friendships, romantic relationships, and work, all while defying society’s expectations.

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27 thoughts on “Born This Way: Moving Forward – Original Casting Footage (Digital Exclusive) | A&E

  1. Don't miss “A Very Born This Way Christmas," the Born This Way series finale Christmas special, airing 12/18 at 9pm ET/PT only on A&E.

  2. I wish they would do different walks of life…that'd be sooooo good for women pregnant with kids with down syndrome, kids in general, and anyone that may not be exposed.

  3. Megan is my favorite TV prison. My. Name is. Jocie. Connolly. I live in St. Charles. 21. Years old. And yes I do you have disability. How long if you have your business. I have a question. ❤️😎

  4. Christina's SUPER WEALTHY family. And megan had a business plan, but couldn't add 2+2. Which is why even with this show no one hires people with mental and physical disabilities. Think about it, the only one with a job was ellena who worked at a charity that specifically gave jobs to the disabled. And Rachel's brothers company came up with a pretend job for rachel to do. She thinks she runs the mail room. Mail rooms haven't existed since 1995. Lol

  5. Megan wants to be a "person who goes out in the real world and does what she wants". Yeah sure she had a business plan. She doesn't even know what that is. Total BS.

  6. Hey girls hey boys goodbye girls are pretty boys and very handsome it's a pretty serious make me happy is pretty but give us funny at Tenison at a big fan of her thank you when was playing when watching us 19 Azan thank you very much I love you guys so I'm just way it going to rain in Mecca restaurant I also

  7. I understand how special need is. My baby brother was a special need and me being the big sister l went to alot things with my brother camping ex… l love the show BORN THIS WAY. BEST EVER. IT BRINGS ALOT OF MEMERIES I DID WITH MY BROTHER. Never take this show off TV. l love everyone in the cast…💙💙💙💙💙

  8. It's hilarious if you watch an interview that Megan gives where the interviewer asks her what university she went to she literally cannot answer that question. The follow-up question is what classes did you take in college and again Megan for the life of her cannot answer or give a single class that she took. It's because this whole new trend of people with Down Syndrome going to college is just another completely made up b***** way to pretend they are just like normal people. Everything about Down syndrome now is just letting them believe they're normal because the reality is they're not normal and they never will be. But if you let them believe they're normal which by the way is not hard to trick them into believing because their IQ is so low.

  9. You can trust the show to create a totally FAKE portrayal of what people with DS are capable of. All this show did was let people with DS kids have FALSE hope on what their kids can accomplish. Silly things like their kids getting jobs is a pipe dream. People with DS DO NOT HAVE JOBS. Despite the huge machine trying to pay businesses to give DS people jobs, it just wasn't happening. So parents of DS adults just start businesses so they can pretend their child has any abilities at all. The reality is they don't, but if you can BELIEVE they do, that's all that matters. Like megan is pretty much worthless as a entrepreneur, but her mom works hard to let Megan pretend she can do stuff.

  10. Megan was a cheerleader…..who became a cheerleader PURELY OUT OR PITY, and wasn't able to do ANYTHING that a real cheerleader would be expected to do. But the reality of things arent as important as the fantasy world they can create and pretend people with DS can do these things. The reality is they CANNOT do these things.

  11. I love watching your families , your children are such an inspiration and have such loving hearts , im comforted knowing they have such wonderful family lives and support and really love following their stories , their lives , please continue and produce another series, ill be waiting lol

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