Alagille Syndrome Alliance
Small but Mighty
Erin Lucca / ALGSA FIGHT for a Better Life 2024
We may be small (in stature and number!) but we are mighty in our efforts to support the Alagille community!
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$7,246
Raised
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$6,000
Goal
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86
Supporters
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27
Days Remaining
Recent Transactions
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Lauren Burgoyne
$103.20 / 2 days ago
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Nafisa Halim
$103.20 / 2 days ago
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Suzanne Sacher
$77.40 / 3 days ago
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Ovi Wagh
$51.60 / 3 days ago
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Tasha Dennison
$51.60 / 3 days ago
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Carolyn Chamberlain
$51.60 / 3 days ago
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Michelle Samplin-Salgado
$103.20 / 4 days ago
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Rachel Wehr
$51.60 / 4 days ago
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Nicole Granger
$25.80 / 4 days ago
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Jennifer Davies
$51.60 / 4 days ago
What a beautiful family supporting such an underresourced cause! Sending love to Kate and team Hasselberg Lucca! x
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Shauna Laskowski
$103.20 / 4 days ago
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Erin Swarbrick
$51.60 / 4 days ago
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Lauren D'Andrea
$25.80 / 4 days ago
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Chia Lin Tan
$106.50 / 5 days ago
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Jeremy Colozzo
$51.60 / 5 days ago
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Arthur Smith
$516.00 / 5 days ago
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Jessica Grohowski
$25.80 / 5 days ago
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Patricia Taylor
$51.60 / 5 days ago
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Elyse Kroon
$20.24 / 5 days ago
About Small but Mighty
Alagille Syndrome is a rare disease caused by a genetic mutation that primarily impacts the functioning of the liver. It is unknown how many people are living today with Alagille. It is estimated to be about 1 in every 30,000 live births or 1 person per every 100,000 (that's maybe 80,000 people globally!). The Alagille Alliance has their work cut out for them! Let's do our part to help them help this amazingly strong and rare community!