Find support in the FA and rare disease community

Patients featured are paid spokespersons for Biogen.

Patient and caregiver support and
advocacy groups

If you need additional support on your Friedreich ataxia (FA) journey, these
organizations may be able to help.*

Caregiver support

National Ataxia Foundation: Care Partners

NAF Care Partners provides guidance, strategies, and resources for those who provide care.

Visit NAF
Global Genes: Rare Disease Community

Global Genes is a nonprofit committed to eliminating the challenges of rare disease by providing information, resources, and connections to all communities affected by rare diseases.

Visit Global Genes
Caregiver Action Network

CAN works to improve the quality of life for family caregivers who care for loved ones with chronic conditions, disabilities, or diseases.

Visit CAN

Advocacy groups

National Ataxia Foundation

NAF specializes in improving the lives of people with ataxia, including FA, through support, education, and research.

Visit NAF
Friedreich’s Ataxia Research Alliance

FARA is dedicated to the pursuit of research to find treatments and a cure for FA.

Visit FARA
National Organizations for Rare Disorders

NORD helps elevate care, advances research, and drives policy change to support and empower people living with rare diseases.

Visit NORD

*This list may not be inclusive of all the organizations that support the Friedreich ataxia community.