Patient Organizations

Connecting with organizations and the larger rare disease community can provide valuable resources, information, and support for parents, families, and patients affected by a central nervous system (CNS) disease diagnosis.*

MPS/MPSIIIA

GM1 / GM2

* This is not intended as a comprehensive list of all global organizations. For assistance finding additional resources, please Contact us.

Lysogene COVID-19 update

Get In Touch

Don’t hesitate to contact us if you need more help.