Our Mission

The Cyclic Vomiting Syndrome Association (CVSA) serves the needs of cyclic vomiting syndrome (CVS) sufferers, their families, and professional care givers by raising awareness and providing education and support to those affected by cyclic vomiting, abdominal migraine, and related disorders, while advocating for and funding research.

Established in 1993, CVSA has grown from a handful of interested parents and professionals into a network that includes over 40 medical advisors and volunteers serving in the U.S. and Canada, as well as over 30 other countries worldwide.

As an association, we have two primary objectives: to work toward a cure by supporting several promising research initiatives, and to assist our members by strengthening communications and offering a wide range of resources for their education and support.

Help further CVS research! Rare Patient Voice has an opportunity to be part of a study!
Cyclic vomiting syndrome Patients and Caregivers
This is a 60 min Web-Assisted Phone Interview and Compensation can be up to $120, Sign up here:

How Does it Work?

Rare Patient Voice helps patients and caregivers voice their opinions through surveys and interviews to improve medical products and services.

rarepatientvoice.com

Your donations at work! This month's presentation Dr. Kovacic will be presenting on the Auricular Stimulator that CVSA helped fund. Learn more about it here: https://t.co/FczYc7smfA Register for the event here: https://t.co/sOy4dGzfve

Only 2 weeks! You can now join CVSA for as little as $25 for the year during our Back to School membership sale. But don't wait too long; the sale ends September 30th! https://t.co/J5G3vo4hcp