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        So far our Annual Campaign has raised $4,140. Every single dollar raised will be matched by Southern Union Company in honor of Rachel Herschmann's 12th birthday and 5-year liver transplant anniversary. But our generous donor will match up to $10,000 in donations, which means we still have $5,860 to go! And we have to raise that $5,860 by February 28th to take full advantage of this awesome offer.

            Remember the little red bag that came in the last issue of Links4Life? Now is the time to drop a check into the return envelope that came with it!

        Alternatively, you may donate online right now by clicking on the Donate button on this page and following the steps on the secure donation page. (On the "Donation Made in the Name of" write "Annual Campaign" then the name of the person you would like to honor or remember.)  Every $1 you donate by February 28th will magically become $2, without any extra effort on your part. What a fantastic way to support our work of funding AGS research and education, and helping everyone with AGS build a better life.

Thank you for
Donating Today and
Raising Hope for Tomorrow!


Annual Fund Raising Campaign Extended
Bulletin Board Server Back Online - 6/4/10
The AGS bulletin board server is back online.  There will be another server down - probably on Monday 6/7/10.  Please watch the website for announcements. Thank you for your patience.
AGS Webmaster

AGS kids page including the slide show!
AGS Bulletin Board Server Update
Upcoming Events
Links4Life Home Page
Click here to go the Links4Life page
Download the latest issue of Links4 Life - click HERE
AGS Gear Now Available!!
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AGS Virtual Walk 2010 - August 15th - October 15th
Make a secure, safe donation to the alliance right now with your credit card.  Click the "DONATE" button below to go to our donation page.
Alagille Syndrome goes national on Ellen
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Go to the AGS Gear hompepage
Donate to the Alagille Syndrome Alliance - Online donation page
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CHOP
American Liver Foundation
AGS in the News
AGS Spotlight: Star of "Team Sophie Alina"
Sophie Alina McGuinness - enjoying a beautiful summer day on Grampa Fernald's boat in Lakeville, MA.  Sophie was diagnosed shortly after birth with AGS. She celebrated her 3rd birthday on May 13, 2009, with a dinosaur theme.  She lives in Midway, MA, with mom Andrea, dad Matthew and baby brother Gavin. Despite all the medication she takes daily and all the doctor's visits with bloodwork and tests, Sophie has a great personality, wonderful imagination, and is sweet, lovable and caring. She loves to be read to, to sing and dance, and to run.  Her favorite color is green, and she loves frogs, dinosaurs, and Thomas the train.  Other than having AGS, she is a typical little girl who brings smiles to everyone she meets.
AGS in the News
Email Us
Tuscon family has big reason to give thanks: their son's health
The Alliance
alagille(at)alagille.org
alagille@alagille.org
New Survey on 2011 Symposium Planning!
The Webmaster
Joey Valente story
agswebmaster@alagille.org
If you shop at Thirty-One Gifts, 10% of your purchase amount will be donated to the Alliance!  Click the link below for more details. 

Limited Time Offer - offer ends February 24th!  Hurry!
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My Thirty-One Site
Get your copy of the latest Links4Life now!
The July-December 2009 issue of Links4Life is now available for download.  If you would like to download the current issue, please follow the link below to our Links4Life page.  Enjoy!
In the News Archives...
Now Enrolling for Study of Alagille Syndrome Liver Disease!
Cast Your Vote for the Alliance on Facebook
Vote for us on Facebook!  Please follow the link below and cast your vote for us on Facebook!  Thanks for voting!
Check out our YouTube page! Click HERE.
Three Important AGS Surveys - please participate!
YouTube videos wanted!
The Alliance has a YouTube channel, but we don't have any content for it at this point.  Do you have anything news worthy or fun for the Alliance's YouTube channel?  If you do, please email the Alliance webmaster.  Thank you!
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