• Featured Highlights
    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...
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  • Featured Highlights
    About this Event June 30th is Arthrogryposis Awareness Day! Please encourage all of your friends and family to wear BLUE on June 30 in honor of all those who live with...
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  • Featured Highlights
    Are you the parent of a child with AMC? Take the survey below to tell us about your prenatal care!Donate Now
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    Celebrate 10 years and still running with Roger’s Run 4 AMC! Due to the Covid-19 Pandemic we will be taking our event virtual this year.  Just because we are going virtual...
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  • Featured Highlights
    Are you excited to know there is research occurring to help improve the lives of people like you or your loved one with arthrogryposis? Get involved and stay connected to what’s happening...
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  • Featured Highlights
    Arthrogryposis Multiplex Congenita Support, Inc. 2018 Membership Form Nationally recognized as an Official 501 (c)(3) Non-Profit Organization All of our programs are fully funded by our AMC community.  We could not do any...
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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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