If I donate to the Alliance, where will the money go?
The Alliance is run solely by volunteers and has no paid staff.
Your donation helps fund Alliance programs and services such as:
Links4Life Newsletter
AGS Family Days
AGS Symposiums
AGS in the Classroom brochures
Operation and maintenance of this website & the AGS server
The Julie Kelin Research & Education Fund
Increasing AGS awareness at various conferences & events
{NASGHAN, NORD, etc.)
Thank you very much for your support!
The information presented on this web site is provided for information purposes only. This information does not constitute medical advice and it should not be relied upon as such. The Alagille Syndrome Alliance does not engage in the practice of medicine. Under no circumstances, does the Alagille SyndromeAlliance recommend particular treatments for specific individuals, and in all cases recommends that you consult your physician before pursuingany course of treatment.
