Connect with people affected by SCA6. Please feel free to email to join the SCA6 Network. See more

SCA6 Information

General information about SCA6 symptoms, testing, diagnosis, cause, and inheritance. See more

Practical Tips

Practical tips for living with SCA6. See more

SCA6 Research

Learn more about SCA6 research. See more

What is our mission?

Our goals

  • Connect people affected by spinocerebellar ataxia type 6 (SCA6)
  • Share SCA6 practical information
  • Provide a forum for discussion about SCA6 research
  • Raise awareness and funding for advancement of SCA6 research to ultimately contribute to better treatments for SCA6.

Groups, Meetings and Events

What's going on

SCA6 Network: We are a group of people who are part of this research group. Many of us have, or have family members who have SCA6 or just want to know more about SCA6. See more

September 25th is International Ataxia Awareness Day

National Ataxia Foundation includes support group events on its Calendar of Events

Latest Developments

Research, publications, trial updates, and news