20th Annual AMCSI Conference
Celebrating 20 years with our AMC family! We cannot wait to see you all! July 9-12, 2025 in Norfolk, Virginia General Registration Is Open! With a condition so rare that only one in 3000 babies born have this neuromuscular disorder, it’s easy to comprehend how alienated anyone with arthrogryposis multiplex congenita (AMC) must feel. Through […]
AMC Events
19th Annual AMCSI Conference
Conference Registration Is Open! With a condition so rare that only one in 3000 babies born have this neuromuscular disorder, it’s easy to comprehend how alienated anyone with arthrogryposis multiplex congenita (AMC) must feel. Through the hard work of one mother’s vision and an army of members, the AMC support group has helped bridge the […]
AMCSI – Meet The Team
About AMCSI — Empowering the Arthrogryposis Community Worldwide
Founded in 2001, AMCSI (Arthrogryposis Multiplex Congenita Support, Inc.) began as a small online group of mothers searching for answers, support, and understanding after their children were diagnosed with Arthrogryposis—a rare, non-progressive congenital condition affecting joint movement. What started as a heartfelt chat among parents has grown into the world’s largest and most trusted online community for AMC awareness, education, and support.
Today, AMCSI connects thousands of individuals and families across the globe, offering expert-backed resources, emotional support, advocacy tools, and life-changing events. Our mission is to ensure no one faces AMC alone. Through our website, conferences, and outreach programs, we continue to spread awareness, promote research, and uplift those affected by this rare condition.
Join us as we champion inclusion, celebrate ability, and provide hope to the AMC community—one story at a time.
