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  • About Moebius »
    • What is Moebius syndrome? »
    • For the newly diagnosed »
    • For infants and children living with Moebius syndrome »
    • For young adults »
    • For adults living with Moebius syndrome »
    • For friends and relatives »
    • For professionals »
    • Treatment options »
  • Who we are »
    • Mission and History »
    • Foundation leadership »
    • Scientific Advisory Board »
    • Press room »
    • Our stories »
    • Financial Overview »
  • Support & Resources »
    • Moebius Syndrome Foundation Educational Scholarship Program »
    • Resources »
    • Connect with Others »
    • Newsletters »
    • Partner organizations »
    • Employment resources »
    • Financial resources »
    • Listing of healthcare service providers »
    • Dental concerns »
    • Talkin’ Moebius Webinars »
    • Moebius Syndrome Foundation Online Store »
  • Events »
    • 2021 Virtual Events »
    • 2021 Moebius Syndrome Foundation Conference »
    • Past Conferences »
    • Regional Events »
    • Moebius Syndrome Awareness Day »
    • Scientific Research Symposiums »
  • Get involved »
    • Join Now »
    • Donate »
    • Moebius Syndrome Foundation Legacy Society »
  • Research »
    • Overview »
    • NIH research study »
    • Scientific Advisory Board »
    • Research symposiums »
    • Research articles »
  • Contact »
  • Videos »
 
 
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What I Want the World to Know About Moebius Syndrome

2021 is still a time where we are staying at home to try and keep the world healthy. This doesn’t mean that we can’t spread awareness about Moebius syndrome and celebrate our differences! Please see the special videos and infographics that we invite the world to see and share as we celebrate MSAD in January 2021.

Infographics

Videos

https://moebiussyndrome.org/wp-content/uploads/2021/01/Addison-Garvey.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Austin.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/David-Garcia.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Jensen.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Jon-Fisher.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Kelsey1.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Rochel.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Leslie.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Violet.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Alex.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Copy-of-Austin.mp4
https://moebiussyndrome.org/wp-content/uploads/2021/01/Soraya.mp4

 

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This is the official website of the Moebius Syndrome Foundation, a 501 (c) 3 organization. The Moebius Syndrome Foundation and its Board does not diagnose Moebius syndrome in individuals nor does it endorse particular medical professionals, treatments, products or services. The Moebius Syndrome Foundation has trademarked its logo and tagline. Expressed written consent is required for use.

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