KIF1A
KIF1A.ORG Kids

KIF1A.ORG is a global community dedicated to improving the lives of those affected by KIF1A Associated Neurological Disorder (KAND) and accelerating research to find a cure.

2025 KAND Conference Presentations

Newly Diagnosed? Register with our organization.

2025 KAND Conference Presentations & slides are available!

Presentations & Slides

Upcoming Events

  • Feb 1 – 28

    Miles that Matter for KIF1A 2026

    Our Miles that Matter fundraiser is BACK in 2026!! Race Info Will You Join Us for Miles That Matter for KIF1A? This February, we’re challenging…

    Sunday, February 1, 2026 – Saturday, February 28, 2026 Participate from anywhere in the world!
  • Feb 12

    Newly Diagnosed Meetup

    These gatherings are open to anyone that is new to our community or any KAND families interested in learning more about our organization’s mission, staff,…

    Thursday, February 12, 2026 12:30 pm – 2:00 pm Eastern Time Zone
    Online via Zoom
  • Feb 18

    1st Quarter Community Call, KIF1A.ORG

    Join us each quarter to dive into current community events, exciting research opportunities, scientific updates, and more! Your participation is essential, and we truly value…

    Wednesday, February 18, 2026 2:00 pm – 3:30 pm Eastern Time Zone
    Online via Zoom
View All Upcoming Events ›

Our Superheroes

Meet some of our superheroes battling KIF1A Associated Neurological Disorder. They’re the bravest people we know.

Sadie
Jaybriel
Susannah
Brayden
Lily
Ashley
Collier
Meet Our Superheroes

Featured in Ken Burns Documentary

The KIF1A.ORG community was recently featured in “The Gene: An Intimate History”, a film about how scientists, doctors and patients are unlocking the power of science to diagnose and treat genetic diseases.

Now more than ever, our world is looking to pioneers and innovators to accelerate scientific breakthroughs that will improve and save lives.

Part One of The Gene highlights the relentless KIF1A.ORG community and our mission to find a cure for KAND.

See Exclusive Clips

Our Impact

0 + people diagnosed with KAND
0 + Research Network Members
0 + countries represented
See Our Impact

On the Blog

January Monthly Momemtum
Monthly Momentum

January Monthly Momemtum

Updates From KIF1A.ORG Happy New Year from all of us at KIF1A.ORG! Our first month of 2026 has been as busy as ever as we look forward to another great year. Thank you for reading as we share what we’ve been up to this month, including: Welcome Our New Fundraising Coordinator, Erin Zaranec! We are…

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December Monthly Momentum
Monthly Momentum

December Monthly Momentum

Updates from KIF1A.ORG What have we been working on during the last month of 2025? Read on below to learn more about what’s been happening at KIF1A.ORG: 2026 KIF1A Community Clinician Survey is LIVE! We are excited to launch our new 2026 KIF1A Community Clinician Survey! This survey is for families to provide information on…

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