Alagille Syndrome Alliance

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The Alagille Syndrome Alliance is an international support and advocacy network for people with ALGS and their families. Mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome.

Founded

1997

Facebook

0

X (Twitter)

387

Address

Collierville

Address: PO Box 22, ColliervilleWeb: Sign in to see organisation websiteX (Twitter): algsallianceEmployees: 2Volunteers: 15Revenue: 571645ICO: 931243619

ALGSA: Leading the Fight for Alagille Syndrome Families World Alagille SyndromeAlliance Our worldwide network of individuals and families affected by ALGS is the heart of our organization Support Alagille Syndrome Awareness with Style. Discover our exclusive collection of clothing and merchandise where every purchase contributes to raising awareness and supporting those affected by Alagille syndrome. Show your solidarity and make a difference with each stylish itemyouchoose. Welcome to ALGSA Welcome to the Alagille Syndrome Alliance ALGSAa dedicated compassionate 501c3 nonprofit organization serving individuals caregivers and families impacted by Alagille Syndrome ALGS around the world.

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News about from their social media (Facebook and X).

Monica

So proud to be part of this amazing community! Together, we're making a difference in the lives of Alagille Syndrome patients and their families. Let's keep pushing for awareness and advocacy! 🌍πŸ’ͺ #ALGSWarriors

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Deborah

Absolutely love what ALGSA is doing for families impacted by Alagille Syndrome! Every piece of merchandise you buy is a step towards raising awareness and supporting those who need it most. πŸ’–πŸ™Œ

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Vera

2. What are some innovative fundraising ideas that can effectively raise awareness and support for Alagille Syndrome research initiatives?

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Terry

1. How can we enhance community engagement and support for families affected by Alagille Syndrome globally?

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