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    Please feel free to share growth data for yourself or your AMCer using the form at https://goo.gl/4XP2q1 . Information is being collected to plot data specifically for AMCers under the age...
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    Welcome to the 3rd International Symposium on Arthrogryposis! The treatment, diagnosis and societal functioning of those with arthrogryposis multiplex congenita (AMC) has changed considerably over the last several decades. Despite that,...
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    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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    Arthrogryposis Multiplex Congenita Support, Inc. 2018 Membership Form *Nationally recognized as an Official 501 (c)(3) Non-Profit Organization*    By becoming a member of AMCSI, you are helping us:   Provide Brochures...
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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.

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