American Cleft Palate Craniofacial Association - ACPA

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American Cleft Palate Craniofacial Association - ACPA

ACPA is leading interdisciplinary cleft and craniofacial care so patients and families thrive.

01/08/2025

Thank you for making National Cleft and Craniofacial Awareness Month unforgettable.

From miles walked to stories shared, YOU made a difference. 💙

Because of your support:
• More people learned about cleft and craniofacial differences
• More families felt seen and supported
• More children received hope and care through ACPA

Let’s carry this awareness into every month of the year.

31/07/2025

Last chance to Color for a Cause!

Awareness Month ends this week—don’t forget to share your finished coloring sheet and tag us to enter our giveaway!

Download your sheet here:
• Girl with Bear: https://bit.ly/45jSaZP
• Boy with Bear: https://bit.ly/44N8fHn

Let’s end July with creativity, courage, and color.

30/07/2025

Throughout July, we’ve shared stories of strength, advocacy, and hope.

In case you missed them, meet some of the incredible Faces of Courage who inspired us this Awareness Month.💙

Didn’t get a chance to share your story? It’s not too late—tag us or submit online at https://bit.ly/3z7EHa1

29/07/2025

Awareness Month is wrapping up—but your impact doesn’t have to.

Here’s how you can stay involved all year:
• Share your story on our website
• Donate or fundraise for care teams
• Advocate for access to treatment
• Sign up for updates and future campaigns

Visit https://bit.ly/3INR7su to stay connected. Together, we can build a world where every smile is supported.

28/07/2025

From her first days in the NICU to brain surgery during the height of a pandemic, Kynslee’s journey has been marked by strength, setbacks, and a smile that never quit.

Born with a cleft lip and palate, Kynslee has faced countless medical challenges: feeding struggles, hip dislocations, multiple surgeries, and a brain cyst diagnosis. But with the support of her family, expert care from an ACPA Approved Team, and her own unstoppable spirit, she’s thriving today.

Her story is a testament to resilience and a reminder of why education, advocacy, and access to care matter.

💜 Read Kynslee’s full story: https://bit.ly/4mhBqZ3
🙌 Support ACPA this Awareness Month and help more children like Kynslee live with confidence, courage, and joy.

Her story is a testament to resilience and a reminder of why education, advocacy, and access to care matter.ity

28/07/2025

Don’t miss your last chance to submit abstracts for ACPA's 2026 Annual Meeting! Abstract submissions are due by tomorrow at 5:00 p.m. ET. Visit the ACPA website https://bit.ly/4e7nSfS for more information about abstract submission.

26/07/2025

Your story has power.

Whether you’ve experienced cleft or craniofacial care firsthand—or as a parent, sibling, or friend—your voice can inspire others.
This Cleft and Craniofacial Awareness Month, we’re inviting you to:
• Post your story
• Tag us
• Use the hashtag

Every story brings us closer to awareness, connection, and compassion.

25/07/2025

🎨 1 Week Left to Color for a Cause!
There’s still time to celebrate Cleft and Craniofacial Awareness Month—get creative and join our coloring sheet activity!

Here’s how:
1️⃣ Download the official sheets at https://bit.ly/45jSaZP and https://bit.ly/44N8fHn
2️⃣ Color it your way (kids and adults welcome!)
3️⃣ Post it and tag to be entered into our drawing!

💙 Every post helps raise awareness for cleft and craniofacial differences. Let’s finish the month strong—one colorful masterpiece at a time!

23/07/2025

Still thinking about joining the 700-Mile Challenge? There’s time to jump in and get moving! 🏃‍♂️

Whether you walk, run, or bike—every mile you log helps support ACPA’s programs for individuals with cleft and craniofacial conditions.

💙 Set your own pace
🌍 Track your miles virtually
🎯 Make a real impact

Sign up today and help us go the distance together!
https://bit.ly/3PX0NCp

23/07/2025

Meet the Cleft Courage Bear—a special companion sent to children born with cleft lip and/or palate. 💙🧸
Every bear represents a child’s strength, bravery, and unique journey.

📦 Want to send a bear to a child you love—or support this meaningful program?
🔗 Visit https://bit.ly/3H2iZbN to learn more.

Let’s celebrate the courage behind every smile.

22/07/2025

Cleft care doesn’t end after one surgery—it’s a lifelong journey.

From feeding support in infancy to speech therapy, dental care, and emotional support in the teen years, every step matters. That’s why ACPA supports team-based, lifelong care so every child with cleft or craniofacial differences gets the support they need to thrive.

💙 Learn more about ACPA Approved Teams and how they help at every stage: https://bit.ly/4f1LN0F

📣 Share this post to raise awareness during Cleft and Craniofacial Awareness Month!

22/07/2025

There’s still time to submit abstracts to present your work on cleft lip/palate and craniofacial anomalies at ACPA’s 2026 Annual Meeting in Boston, MA!

Submit your abstracts by 5:00 p.m. ET on July 29.

Please visit the ACPA website to review important information about abstract submission if you haven't done so already. https://bit.ly/4e7nSfS

Address

510 Meadowmont Village Cir, Suite 377
NC
27517

Opening Hours

Monday	09:00 - 17:00
Tuesday	09:00 - 17:00
Wednesday	09:00 - 17:00
Thursday	09:00 - 17:00
Friday	09:00 - 17:00

Telephone

+19199339044

Website

https://linktr.ee/ACPAcares

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