Curing, treating & connecting
is Positively Possible
  • Connecting is happening

    Positively Possible:
    Bringing together the best of science and patient stories to solve NGLY1’s challenges

    We are looking for a postdoc!

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    Patient Stories

    If you are a patient or think you know one, we are here to help

    Citizen Science

    Mark2Cure: community and technology make a difference for NGLY1


    NGLY1 featured in The New Yorker: One of a kind

    Key Symptoms

    Hyperkinetic movement disorder, developmental delay, dry eyes and history of elevated liver function

    Key Research

    Participate in the NGLY1 Natural History Study

    Help Now

    Your donation makes diagnosis, research, treatment and support possible

    Sharing is Happening

    Positively Possible:
    The NGLY1 community continues to grow thanks to all the contributors to this website. Our children are grateful for your support!