Megan Hayes (full Trisomy 18) Turns 40 years Old! | SOFT
Megan Hayes (full Trisomy 18) Turns 40 years Old! | SOFT
Mar 4, 2023
trisomy.org
79K 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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79K views · 3.1K reactions | Heidi was born with an extra 18th chrom…
79.8K views3 weeks ago
FacebookSpecial Books by Special Kids
Trisomy 18 has an over 90% termination rate. Often parents are told their child is suffering if they do not abort. They are scared into believing that having a child with a disability will ruin their lives. They are worried that watching their child pass away will break them. I am here to tell you that God is with you. Whatever your child’s story, your only job is to love and protect them while they are here. #trisomy18 #specialneedsfamily #obgyn #highriskpregnancy #medicallycomplexkids #medical
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Trisomy 18 has an over 90% termination rate. Often parents ar…
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FacebookAlexander the Great Trisomy 18 Story
5 things you should know when you get a Trisomy 18 diagnosis- 1. Don’t let them steal your hope. Trisomy 18 is not a death sentence. 2. Trisomy 18 babies have a better chance of survival with medical interventions like any other child. University of Michigan has 90% survival rate to their 1st birthday. 3. You will never wish you had less time with your child. Doctors who treat T18 children regularly say they are the happiest children they see. 4. There are thousands of Trisomy 18 children and ad
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FacebookBorn Abel
I’m still in shock at the ignorance of some grown adults. #disabilityrights #specialneeds | Alexander the Great Trisomy 18 Story
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I’m still in shock at the ignorance of some grown adults. #disabilityrigh…
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FacebookAlexander the Great Trisomy 18 Story
It was a big day for Alex today! CPAP may not be a big deal for adults, but it can be hard on a little kid. Alex was born with a smaller upper airway which made his breathing dangerous at night when he was asleep. He wore CPAP for many years until finally he was strong enough to rip it off his own face every night. After much deliberation, the decision was made to surgically correct his airway because he just wasn’t tolerating CPAP therapy. His surgery WORKED! Alex now breathes peacefully and no
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It was a big day for Alex today! CPAP may not be a big deal for ad…
8.4K viewsAug 24, 2023
FacebookAlexander the Great Trisomy 18 Story
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2.3K views · 374 reactions | Having a child who is medically complex...
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