Our mission is creating safe, effective, and accessible treatments for all individuals with DYNC1H1 disorders.
The DYNC1H1 Association (DA) is a non-profit patient advocacy group
We envision a world where anyone with a DYNC1H1 Variant has a safe & effective treatment.
Our Mission:
Create opportunities for research on DYNC1H1 with a constant drive towards low-risk, high reward treatments.
Our Commitment:
Forge networks of support within the diagnosed persons, providers, and researchers to make the wait easier.
We need your help to follow our path to a cure.
If you or your child have DYNC1H1 Variants, join our Patient Registry so that we can stay in contact and ensure we are addressing the needs of all individuals with DYNC1H1 related disorders.
Join Simons Searchlight to help us be ready for clinical trials once likely treatments are found.
Share your story and be featured as a “Patient of the Week” on our Social Media. Email contact@dync1h1.org
Donate or create a fundraising team to support our research efforts.
For more information on how to get involved and our goals, go here.
The DA is run by volunteers whose children have DYNC1H1 Disorders, along with an incredible Scientific Advisory Board. The SAB includes clinicians and researchers who are experts in DYNC1H1, dynein (the protein product of the DYNC1H1 gene) & cellular trafficking, epilepsy, and neurological disorders. With this expert guidance, we are making strides towards cures for DYNC1H1 Disorders.
The DA has also cultivated key partnerships with complementary organizations. These organizations include other rare disease networks, research-enabling organizations, and groups with expertise in building clinical trial readiness.
Meet the Founders
Lisa Costen, MS
Founder & President
Brettne Frewin
Founder & CFO
Liz Spitzer, PhD
Founder & COO
Our Partners
The DA’s Scientific Advisory Board
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Erika Holzbaur, PhD
University of Pennsylvania
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Morgan DeSantis, PhD
University of Michigan
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Hormos Salimi Dafsari, MD
Pediatric Neurology and Center for Rare Diseases at University Hospital Cologne and Max-Planck-Institute for Biology of Aging
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Steven Markus, PhD
Colorado State University
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Christelle Moufawad El Achkar, MD
Epilepsy Center, Department of Neurology, Boston Children’s Hospital
Instructor of Neurology, Harvard Medical School
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Majid Hafezparast, PhD
University of Sussex, Brighton, UK
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Rozalia Valentine, MS, CGC
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Gyula Ascadi, MD
Pediatric Neurology, Connecticut Children’s Medical Center Research Institute
Our Families Need You!
Without your generous help, we cannot make this world an easier place for those with DYNC1H1-associated neurological disorders. This is an urgent plea from a community living with a debilitating and degenerative disease. Please help us by donating today.
Contact Us
Want to get in touch? We’re a small organization always interested in new partnerships, volunteers, and simply getting to know our community. Send us a note in the contact form, email, or write!
Contact@dync1h1.org
PO Box 834
Orange, CT 06477 USA