Edwards syndrome (Trisomy 18): Video, Causes, & Meaning | Osmosis
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Edwards syndrome (Trisomy 18): Video, Causes, & Meaning | Osmo…
已浏览 18 次2021年2月9日
osmosis.org
Megan Hayes (full Trisomy 18) Turns 40 years Old! | SOFT
Megan Hayes (full Trisomy 18) Turns 40 years Old! | SOFT
2023年3月4日
trisomy.org
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bb4d6e4c-96b8-40ed-b6c3-f6178fa0adf9
4 个月之前
bartleby.com
80K views · 3.1K reactions | Heidi was born with an extra 18th chromosome, a condition known as Trisomy 18. After she was diagnosed in-utero, her parents were told that she "wouldn't be very human-like". They decided to just love Heidi unconditionally. Heidi is now 6 years old and her family is proud of everything she does, like using sign language to communicate. | Special Books by Special Kids | Facebook
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80K views · 3.1K reactions | Heidi was born with an extra 18th chrom…
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FacebookSpecial Books by Special Kids
Knoxville baby born with Trisomy 18 defies odds, inspires mothers to support other parents
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Knoxville baby born with Trisomy 18 defies odds, inspires mothers to s…
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MSNWBIR-TV Knoxville
I am a Trisomy 18 mom. It wasn’t a tragedy. It wasn’t horrific. I was chosen to be the mom of a very special little boy, and I would never change that in a million years. Oren will always have the memories and pictures of his twin brother. My children all got to know Abel. His life, although too short, will be forever cherished, and he changed our lives forever. Trisomy 18 parents… we are blessed with little angels earth side. Whether we get them for minutes, hours, days, years or decades… We ar
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I am a Trisomy 18 mom. It wasn’t a tragedy. It wasn’t horrific. I was ch…
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FacebookBorn Abel
"We had 15 days with her that was not supposed to be, and it was the closest to God that we have ever been." A profoundly moving story of a family who chose life for their unborn daughter after she was diagnosed with Trisomy 18. Check out more inspiring stories from Moving Works at: www.movingworks.org OR: www.facebook.com/movingworks. | Focus on the Family New Zealand
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"We had 15 days with her that was not supposed to be, and it was th…
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FacebookFocus on the Family New Zealand
'Worth every minute': Parents of babies with trisomy 18 say they d…
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This my beautiful daughter, Everly. she has Trisomy 18. Trisomy 18 i…
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The Edwards’ Syndrome focuses entirely on Trisomy 18, so this is o…
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