I Gave the Gift of Hope — CACNA1A Foundation

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What is CACNA1A?

CACNA1A-Related Disorders

Understanding Variant classification on a Genetic Report

Family & Scientific Conference 2024

Family & Scientific Conference 2022

Family & Scientific Conference 2021

Newly Diagnosed

Participate in Research

Contact Registry

CACNA1A Champion Stories

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CACNA1A World Map

Global Research Network

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Could it be CACNA1A? Free Genetic Testing

Family and Scientific Conference 2026

Community Conversations

Awareness Day: March 19

5 Boro Bike Tour

Run, Walk & Roll

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Board and Leadership

Scientific & Medical Advisory Board

Global Ambassadors

Clinician Resources

Hemiplegic Migraine Resources

Find a Physician

Informational Handouts

Scientific & Medical Journal Articles

Resources and Funding for Families

What is CACNA1A?

CACNA1A-Related Disorders

Understanding Variant classification on a Genetic Report

Family & Scientific Conference 2024

Family & Scientific Conference 2022

Family & Scientific Conference 2021

Newly Diagnosed

Participate in Research

Contact Registry

CACNA1A Champion Stories

Submit Your Story

CACNA1A World Map

Global Research Network

Research Grant Program

Research Grant Funding Recipients

Could it be CACNA1A? Free Genetic Testing

Family and Scientific Conference 2026

Community Conversations

Awareness Day: March 19

5 Boro Bike Tour

Run, Walk & Roll

Shop our CACNA1A Store

Board and Leadership

Scientific & Medical Advisory Board

Global Ambassadors

Clinician Resources

Hemiplegic Migraine Resources

Find a Physician

Informational Handouts

Scientific & Medical Journal Articles

Resources and Funding for Families

Folder: Learn About CACNA1A

What is CACNA1A?

CACNA1A-Related Disorders

Understanding Variant classification on a Genetic Report

Family & Scientific Conference 2024

Family & Scientific Conference 2022

Family & Scientific Conference 2021

Folder: Families & Caregivers

Newly Diagnosed

Participate in Research

Contact Registry

CACNA1A Champion Stories

Submit Your Story

CACNA1A World Map

Folder: Research

Global Research Network

Research Grant Program

Research Grant Funding Recipients

Could it be CACNA1A? Free Genetic Testing

Folder: Get Involved

Family and Scientific Conference 2026

Community Conversations

Awareness Day: March 19

5 Boro Bike Tour

Run, Walk & Roll

Shop our CACNA1A Store

Folder: About Us

Board and Leadership

Scientific & Medical Advisory Board

Global Ambassadors

Folder: Resources

Clinician Resources

Hemiplegic Migraine Resources

Find a Physician

Informational Handouts

Scientific & Medical Journal Articles

Resources and Funding for Families

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CACNA1A Foundation

CACNA1A Foundation is a parent-led 501(c)(3) non-profit. We are dedicated to creating awareness and finding a cure for CACNA1A genetic variants.

info@cacna1a.org

CACNA1A Foundation, Inc.

31 Point Road

Norwalk, CT 06854 USA

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This site is intended to provide basic educational information about CACNA1A-related disorders. It is not intended to, nor does it, constitute medical or other advice. Readers are warned not to take any action with regard to medical treatment or otherwise based on the information on this web site without first consulting a physician. The CACNA1A Foundation does not promote or recommend any treatment, therapy, institution or health care plan.

The information contained in this site is intended for your general education and information only and not for use in pursuing any treatment or course of action. Ultimately, the course of action in treating a given patient must be individualized after a thorough discussion with the patient’s physician(s).