• Featured Highlights
    The treatment of arthrogryposis multiplex congenita (AMC) related disabilities are under represented and under examined, compared to other neuromuscular conditions. Worldwide, there are few patient support/advocacy groups for AMC, and most...
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  • Featured Highlights
    Just in time for the holidays! Purchase this pewter ornament for $20 and $5 will go directly to help offset the costs of our annual AMC conference   Click here to...
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  • Featured Highlights
    Every act of giving has a story… what is yours? #MyGivingStory is a social media storytelling contest created to foster a public conversation about giving and to inspire more people to...
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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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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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