• Featured Highlights
    An AMAZING short film about Arthrogryposis Multiplex Congenita in children and youth. Thank you McGill University Faculty of Medicine Summer 2017 Research Bursary Program for awarding Sabrina Shemie the Sir Edward...
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  • Featured Highlights
    About Conference 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...
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  • Featured Highlights
    Arthrogryposis Multiplex Congenita Support, Inc. 2017 Membership Form *Nationally recognized as an Official 501 (c)(3) Non-Profit Organization*   By Becoming a Member of AMCSI you are helping us: Provide our AMC families support,...
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  • Featured Highlights
    AMC Awareness Day Proclamation FAQ What is a proclamation? A proclamation is a formal public statement. It is a major statement made in front of an audience or the authoritative word...
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OUR MISSION

To provide and encourage more understanding and mutual support among anyone affected with the diagnosis of arthrogryposis multiplex congenita (AMC). To create a higher standard of AMC awareness by means of conferences, meetings, and studies.

 

 

OUR VISION

To provide educational material to new parents, or soon-to-be parents regarding the diagnosis of arthrogryposis multiplex congenita (AMC).

To provide a resource of information to the medical field to include, but not limited to, occupational therapists, physical therapists to assist them in the treatment of a child or person with the diagnosis of AMC.

Blog

Get the latest news, tips and etc. on our blog.

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