HAPPY NATIONAL CLEFT AND CRANIOFACIAL AWARENESS MONTH!!! I wish all my fellow cleft people a wonderful month full of joy <3
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HAPPY NATIONAL CLEFT AND CRANIOFACIAL AWARENESS MONTH!!! I wish all my fellow cleft people a wonderful month full of joy <3

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happy cleft and craniofacial awareness month to all the cleft&craniofacial girlies who were forced to go through speech therapy
Getting A Head
3D imaging combined with tissue clearing and immunostaining reveals the development of the head and its organs as a human embryo grows – insight into understanding craniofacial defects and neurological disorders, and how to diagnose and treat them
Read the published research article here
Image from work by Raphael Blain and colleagues
Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France
Image originally published with a Creative Commons Attribution 4.0 International (CC BY-NC 4.0)
Published in Cell, December 2023
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"Your soul is a beautiful thing, child," replied the grave man's voice, "and I thank you."
A new study has investigated the genetics of the cleft lip, a relatively common physical defect in humans, developed at birth. This work also highlights the importance of molecular regulators, such as histone modification, in normal embryonic development.

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it's so real that i was born in craniofacial awareness month, i was born to slay mouth breathing and 11 surgeries
I've only met two other people with cleft palates (both on this app) and while all of our experiences have been different, I'm glad to know that we're all connected by our lack of representation in media and our hate for speech therapy
did not realize there was a community for this, but this is the internet i should've known
hi i was born with a cleft soft and hard palate, i didn't have a cleft lip or anything else (still tagging this because i wanna reach anyone who understands), my mom told me that i also have the thing where you have a really small chin combined with a cleft palate but i don't remember the name of the condition
i've like literally never been able to talk to anyone else who's had one and i mean my friends all know about it and i love them, but like they don't fully understand bc they haven't experienced it, you know how it is
but uh yeah i've always felt really weird labeling myself as like disabled or anything like that because i've always felt like my cleft palate wasn't enough but honestly my entire life has kinda revolved around it so i feel like i should
here's the part where i'm going to dump in a list all of my super specific experiences in hopes that someone will relate because i am so serious when i say that i've never talked to someone who relates before:
tw: idk medical stuff, ed mentioned (arfid specifically), mildly graphic i guess (just complaining about medical stuff i've had to deal with)