Support ALGSA and show your WARRIOR pride with our collection of gifts, accessories and more! Shipping to the USA, Canada, Australia and most European countries.

The ALGSA Warrior Shop

Support our Warrior Shop and help to fund our Mission:          Mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome.

SUPPORT THE WARRIORS

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The Walker Family in ALGS Warrior Gear.

WHO IS AN ALAGILLE WARRIOR?

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MESSAGES FROM OUR ALGSA COMMUNITY

Erika from Denmark.  Alagille Warrior.

Rare Disease Reality ...

'I have learned that sometimes I know more about my rare disease than the skilled doctors I meet on my journey.  This means that I often have to share my knowledge about my illness with my medical team'  

~ Erika (Denmark)

learn more about alagille on OUR WEBSITE
Shamy from India.  Alagille Warrior.

A Global Community ...

'The ALGSA connects you to information. It’s an incredibly dedicated team of people that believe in the ALGSA vision of supporting and caring for people.  The Alagille Syndrome Alliance gave me the support I never had.'

~ Shambhavi (India)

Read Shambhavi's Story on Facebook
Tiffany and Malee.  Alagille Warriors.

Parents searching for answers ...

'Currently there is no cure for Alagille Syndrome, we continue to search for answers. ALGS is incredibly rare and funding is extremely limited but researchers are identifying potential therapeutic avenues'

~ Malee's Mom Tiffany (USA)

Read Malee's story on instagram