TCS mission

Spreading awareness about Treacher Collins Syndrome "one step at a time, together we can educate each other about TCS"

[CCAKids - Children's Craniofacial Association @CCAKidsTweet]

Be part of the change you want to see in the world

[TCS mission @TCSaware]

Everyone is beautiful in their own ways, inside and out!
#FacialEquality

[TCS mission @TCSaware]

What is TCS? It is a genetic disorder that affects the development of bone and tissue

To learn more visit https://t.co/7uqypjQvMb

[TCS mission @TCSaware]

Start the new year off with educating yourself on Treacher Collins Syndrome!
Visit https://t.co/qVSMzGKZuD to learn more #treachercollinssyndrome #craniofacial

[Face Equality International @FaceEqualityInt]

Open & honest interview with @Gailporter on hair loss and alopecia. 🙌

#FaceEquality

[CleftProud @CleftProud]

💙 (Story): “Hi! My name is Dennis and was born in Taiwan with an unilateral cleft lip and palate. My mother and I migrated to the US when I was 11. Growing up was tough emotionally and faced challenges that would… https://t.co/CVuU5089Zu

[TCS mission @TCSaware]

You can help patients with Treacher Collins Syndrome by donating to the Children's Craniofacial Association! @CCAKidsTweet #TCS #FacialEquality
https://t.co/7uqypjQvMb

[Changing Faces @FaceEquality]

“Talking is the best thing to do.”

The wonderful Gail Porter with a message of positivity for any women struggling with hair loss.🦋

https://t.co/P0wteFM6SR

[Paul Trainor @aussiebiologist]

The National Organization for Rare Disorders (NORD) has updated its Rare Disease Database report on Treacher Collins Syndrome.

Find out the latest information on key genes and TCS research.
@TCSAwareness

https://t.co/TpkzGh0iCz

[Operation Smile @operationsmile]

Thanks to you, conducted 176 medical programs across 103 sites in 32 countries in 2019. Of that total, 112 missions were conducted by a majority of local medical volunteers. Among them was Andrea, who received #cleft #surgery at 38-years-old. Read more https://t.co/4s5k91nvzF

[TCS mission @TCSaware]

Do you know which genes are mutated to cause Treacher Collins Syndrome? Visit https://t.co/7uqypjQvMb for informations about the three genes #themoreyouknow #treachercollinssyndrome #craniofacial

[CleftProud @CleftProud]

💙 (Story): “Hi everyone! I’m stella, i'm 16, and i was born with a unilateral cleft lip and palate. Growing up, i was made fun of a lot for how i looked and my mental health suffered a lot. But then i found singing… https://t.co/iOjtJ5tHRZ

[CleftProud @CleftProud]

💙 (Story): “Hello! My name is Chloé, I’m 20 years old and I’m from the southwest of France. I was born with a unilateral cleft lip. I’ve had 3 surgeries in Toulouse and I will have another one with a new surgeon in… https://t.co/fFRFXJROwZ

[CleftProud @CleftProud]

💙 (Story): “Hi! I’m Erin. I was born with a unilateral cleft lip and just discovered this page. I wish I had discovered it sooner. I live in PEI, Canada where I hardly ever see other people with a cleft lip. I’ve had… https://t.co/UPUHRTsCXR

[CleftProud @CleftProud]

💙 (Story): “Hi, my name is Rhett and I am #CleftProud!!! My mommy found out I was going to be born with a unilateral cleft lip at her 20 wk sono. I could feel her emotions flare but when she found out she was having… https://t.co/hyrZb4giNN

[CleftProud @CleftProud]

💙 (Story): “Hi! My name is Felicia, im 18 years old and from sweden. I was born with a bilateral cleft lip and palate. I dont know how many surgeries i've had but i think its well over… https://t.co/wSqVBaf21p

[DevelopmentalDynamic @DevelopmentalDy]

Cleft lip and palate are among the most common human birth defects, but their underlying etiology is poorly understood. Learn how the intersection of morphology, gene expression, and DNA methylation contributes to the pathogenesis of orofacial clefting.
https://t.co/yCNr63ycRw

[TCS mission @TCSaware]

Did YOU know Auggie in the book Wonder has Treacher Collins Syndrome? Learn more about Treacher Collins Syndrome by visiting https://t.co/7uqypjQvMb

#treachercollinssyndrome #FacailEquality #wonder

[Shriners Children's Chicago @ShrinersChicago]

"The boys (Peter and Aaron) who used to ride bikes all around their neighborhood learned to cope with their new lives and relearned things that were so simple before - how to get out of bed and how to get dressed."

[Shriners Children's Chicago @ShrinersChicago]

Watch Mason save #buzzlightyear during #physicaltherapy. He is relearning to walk. M's parents are pros at getting him to work to be stronger w/ our #orthopaedics #rehabilitation & POPS teams. https://t.co/ITlkKKwYa2 @shrinershosp