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Born This Way: Official First Look – Tuesdays 10/9c | A&E

   January 4, 2022  12 Comments on Born This Way: Official First Look – Tuesdays 10/9c | A&E

Catch the new series Born This Way on Tuesday, December 8th at 10/9c. This series offers an intimate look into the lives of young men and women born with Down Syndrome.

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12 thoughts on “Born This Way: Official First Look – Tuesdays 10/9c | A&E”

  4. I love how no one will be honest with megan as to why she shouldn't have a child. She's been lied to her whole life in the name of self-esteem, that she probably doesn't even realize that she can't possibly take care of herself. She truly believes she lives with her mom to keep her company – not because she would die in a week left all alone. Megan believes so much of what her mom tells her that she doesn't understand why she can't have a baby. Most people would think that she'd know that since she can't even feed herself or get anywhere by herself that it would be obvious to her. But it's not, and her mom still refuses to talk realistically about it. She just keeps giving her other excuses why she can't have a baby. The only reason she needs to give her is that Megan can't even take care of herself so how does she expect to take care of a baby? Her mom is already exhausted from running her daughters company for her. She doesn't have time to raise a granddaughter with mental disabilities too.

  5. Can A&E start paying all the money the cast collects in benefits so the taxpayers can stop paying so much for these people to achieve their dreams without actually having a real job. I get that they have the intelligence of a 3yr old, so they believe they deserve their own house for free, but why do we have to pay for it? Because they are not able to take care of themselves. So then why do we have this fake show trying to pretend they can do anything for themselves when they really can't.

  6. I have a nine year old daughter (Kayla) with DS. Not only is this a treat for me to see what she may be like when she gets older but I think it is a huge step forward for all kids with DS to show the general public what our precious children have to offer this world.I know it has made me a better person.

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