Multimedia Library

FULL COLLECTION | Expert | LCN | Downloads | Videos | Podcasts | Instagram | Spotlight |

Instagram

LCN’s recent Instagram feed. Click on an image to read the caption — no social media account required!

View fullsize LCN is excited to announce the launch of a new Multimedia Library on our website! This comprehensive section features expert articles, LCN news, downloads, podcasts, videos, and interesting people and stories relevant to the laryngeal cleft communit
View fullsize Today is a special day: Laryngeal cleft hero Markus is celebrating his golden birthday! Please join us in wishing Markus a wonderful, spectacular day. You can read Markus’ type 4 cleft journey here: https://www.laryngealcleft.org/type-4-jour
View fullsize LCN is honored to share the type 1 laryngeal cleft journey of Olivia. “Olivia was born a healthy (or so we thought) baby weighing 9 pounds 3 ounces. At two weeks old, we brought her to the pediatrician regarding possible acid reflux or a pote
View fullsize
View fullsize Want to be part of the solution? Attend the LCN Community Outreach meeting tomorrow! When: Sunday, May 18, 4 pm EST Bring your valuable opinions and ideas to help guide LCN programs and projects. There is no time commitment required. To receive t
View fullsize Accessing a medical provider who is experienced in treating laryngeal clefts may require travel. LCN has identified numerous organizations that exist to help families facing medical challenges. Some cover transportation costs, including free airpla
View fullsize Happy International Nurses Day! Nurses play an important role in the journey of many children and people with a laryngeal cleft. On International Nurses Day, we want to acknowledge the care, advocacy, compassion, guidance, and reassurance nurses p
View fullsize Happy Mother’s Day to all of the incredible moms in our community who work so hard for their child. Motherhood is unquestionably an incredible gift. And like everything in life, it’s not always easy. As a mom of a child with a laryngeal
View fullsize Laryngeal Cleft Network is honored to support the journey of Olivia, a hero born with a type 1 laryngeal cleft. “The LCN grant was incredibly beneficial to our family, as it allowed us to stay overnight before our daughter Olivia's surgery. T
View fullsize Today is a special day: laryngeal cleft hero Olivia is 1 year old! Please join us in celebrating Olivia on her big day. 🎂🎉🩷 HAPPY BIRTHDAY OLIVIA! Wishing you a bright and wonderful year! (Request a birthday post for your laryngeal cleft he
View fullsize Want to be part of the solution? Attend the next Community Outreach meeting! When: Sunday, May 18, 4 pm EST Bring your valuable opinions and ideas to help guide LCN programs and projects. There is no time commitment required. To receive the meeti
View fullsize Happy National Speech-Language-Hearing month! LCN extends our heartfelt appreciation to the many speech-language pathologists and audiologists who work so hard to help children born with a laryngeal cleft. Your efforts to help our kids swallow safe
View fullsize So True. #laryngealcleftnetwork #laryngealcleft #journeysmatter #closethegap #thehiddencleft
View fullsize April is Autism Acceptance Month, and autism is part of the journey for some children with a laryngeal cleft. Autism acceptance means understanding and embracing all people on the autism spectrum and acknowledging their unique strengths and challeng
View fullsize Today, as LCN celebrates our beautiful planet, we want to shine the light on how closely environmental health is connected to personal health. For those born with a laryngeal cleft, every breath can be a little more difficult—and polluted air
View fullsize Don’t forget... ...RARE Bear orders are due tomorrow, April 22! Visit LCN’s website to order yours today: https://www.laryngealcleft.org/rare-bears RARE Bears are offered twice a year to our laryngeal cleft community through LCN’
View fullsize April 20-26 is National Volunteer Week. So much of what we do at Laryngeal Cleft Network is made possible by our wonderful network of volunteers. These volunteers play a vital role in helping raise awareness about The Hidden Cleft. Thank you to al
View fullsize LCN is honored to share the type 1 laryngeal cleft journey of Aubriana. “In her first few days of life, we noticed she struggled to take bottles. Doctors assured us babies can be tricky, and she was simply not used to it yet.” Seven mon
View fullsize Today is World Voice Day. As parents of a child with a laryngeal cleft, our voices are crucial. Our voices have the power to: 🔹 convey love and reassurance to our child. 🔹 communicate with our child’s care team. 🔹 advocate on our child&rs
View fullsize Please share to build AWARENESS! #laryngealcleft #laryngealcleftnetwork #thehiddencleft #closethegap #laryngealcleftawareness