We are working on an exclusive site for our AGS kids. Look for more information about the site here.
In the meantime, please take a look at our AGS heroes slideshow. If your child is not featured in the slideshow and you want them to be, please email your digital picture to the AGS Webmaster (see email below). Thanks!
Erik
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.
