Patient Advocacy Groups h1 >
![CDG CARE logo](https://static.rarediseasesnetwork.org/logos-pags/Logo-PAG-CDGCARE.jpg)
CDG CARE (Community Alliance and Resource Exchange)
Promotes awareness of congenital disorders of glycosylation (CDG) and NGLY1-deficiency, provides resources, and funds scientific research.
![logo](https://static.rarediseasesnetwork.org/logos-pags/FCDGC_PAGs__Logos_CDG-Allies-PPAIN_543x196.png)
CDG & Allies - PPAIN
A patient-led infrastructure for research, awareness, and education for Congenital Disorders of Glycosylation.
![logo](https://static.rarediseasesnetwork.org/logos-pags/CDG_canada_colour_logo.png)
CDG Canada
Connects patients and families affected by congenital disorders of glycosylation (CDG) to clinicians and researchers in Canada and globally.
![logo](https://static.rarediseasesnetwork.org/logos-pags/Logo-PAG-AmourFund.jpg)
Amour Fund
Funds research for congenital disorders of glycosylation (CDG), advocates for screening, raises awareness, and assists families.