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Team Small but Mighty – Importance of Patient and Family Involvement in Fundraising Initiatives Q & A

Team Small but Mighty – Importance of Patient and Family Involvement in Fundraising Initiatives Q & A

by Roberta Smith | May 14, 2024 | ALGSA

Learn why ALGS Mom, Erin Hasselberg Lucca, participates in the Fight for a Better Life campaign each year and how she views working in partnership as a parent to advocate and raise awareness for patients and families and the ALGSA. Q. What is your relationship to...
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ALGSA | USA

The Alagille Syndrome Alliance is a nonprofit corporation with federal tax exempt status as a public charity under section 501(c)(3).

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Mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome.

ALGSA | USA

To continue to pursue a cure for ALGS and improve the lives of ALGS Warriors everywhere including ending itching forever!

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ALGSA | USA

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Alagille Syndrome Alliance
P.O. Box 22
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Email: alagille@alagille.org
Phone: 989.218.9028

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