Avery Biomedical Devices, Inc.

06/02/2026

June is .

Myasthenia gravis is a rare disease that causes fluctuating fatigue and weakness in voluntary muscles, like those in the face, neck, throat, diaphragm, and limbs. It happens when the body’s immune system creates antibodies that disrupt communication between nerves and muscles, making it difficult for muscles to contract.

Symptoms may include drooping eyelids, double vision, difficulty speaking or swallowing, and trouble lifting objects. Although there is no cure for , treatments can help relieve symptoms and, in some cases, lead to remission.

To learn more about myasthenia gravis, and how our in the Gregory W. Fulton ALS and Center can help, visit https://bar.rw/myastheniagravis.

(🎨: Barrow Publications)

06/01/2026

June is Myasthenia Gravis Awareness Month 💙

This month, we recognize the strength and resilience of those living with Myasthenia Gravis (MG), a rare neuromuscular disease that affects muscle strength and everyday activities. By raising awareness, supporting research, and sharing stories, we can help improve the lives of those impacted by MG.

Join us in spreading awareness and supporting the MG community throughout June. Together, we can make a difference.

05/27/2026

05/26/2026

Voting is now open for the 2026 CCHS Day T-Shirt Contest! Voting begins today and closes on May 31 at 11:59 PM. Make your voice heard and help us select this year’s winning design… Click below to cast your vote: https://form.typeform.com/to/bctKyiGG See less

05/25/2026

This Memorial Day, we remember and honor those who served our country. We’re grateful for their sacrifice and the freedoms we enjoy today.

05/21/2026

Our DME Grant helps individuals with CCHS access essential durable medical equipment when insurance coverage falls short, providing up to $5,000 per year. Visit our website to learn more about eligibility and how to apply at https://cchsnetwork.org/cchs-durable-medical-equipment-grant-application/.

05/20/2026

We are a family-run organization supporting children, adults, and families living with CCHS, a lifelong condition affecting over 4,000 families worldwide. Our goal is to ensure that no one faces this journey alone. We provide peer support, family education, research advocacy, and the steady community no one finds on diagnosis day. Learn more about us at cchsnetwork.org.

05/15/2026

Owl City - Fireflies (Last.fm Sessions)
https://youtu.be/M94XFqsKGhk?si=jN2mld3-kMVdNyNB

04/17/2026

Today we acknowledge as our Family Resource Center turns red from April 16–18. As our Hemophilia Treatment Center celebrates its 60th anniversary this year, we honor and support those living with hemophilia, a rare, lifelong bleeding disorder. Learn more about hemophilia and our Hemophilia Treatment Center.
🔗 https://www.cincinnatichildrens.org/health/h/hemophilia