Connect with us...

    

 

ALGS Kids rock!

  

 

View and download the latest version of our newsletter, Links4Life

 

Keep us top rated
for 2016. Click on
the logo above to
share your comments
about the ALGSA.
Thank  you!

Email this page to a friend
module by Spiral

Please contact us if you move, if your email address changes, if you want to receive our newsletter or just need some advice and or help.  You can contact the Alliance at the following address or use the contact form below. 

Cindy L. Hahn, CEO

Alagille Syndrome Alliance

10500 SW Starr Drive

Tualatin, OR  97062

ph: 503.885.0455

email: alagille(at)alagille.org

 No faxes please.

The best time to call is between 9 a.m. and  noon Pacific time, Monday - Friday.


Follow us on Twitter

Symposium Countdown

config

Donate safely and securely online now.

Thank you!

  

 

 Do you shop on Amazon.com?  If you do, why not let Amazon donate a portion of the total sale to the Alagille Syndrome Alliance?  The money will be used to benefit ALGSA families.  

View our donation page for more information on what the donated money is used for. 

 

To use Amazon Smile, browse to http://smile.amazon.com. Sign in to your account and select Alagille Syndrome Alliance as the charity of your choice.  Thank you!

 

Home | Site Updates | Site Map

 

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. 

The information presented on this website 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 Syndrome Alliance recommend particular treatments for specific individuals, and in all cases recommends that you consult your physician before pursuing any course of treatment.

 

Copyright © 1998 - 2016. The Alagille Syndrome Alliance - All Rights Reserved.