Alagille Syndrome Alliance

About Alagille Syndrome Alliance

The Alagille Syndrome Alliance (ALGSA) is a compassionate nonprofit organization dedicated to supporting individuals, caregivers, and families impacted by Alagille Syndrome (ALGS). With a global reach, ALGSA stands at the forefront of the fight against this rare genetic disorder, providing invaluable resources and fostering a sense of community among those affected.

Impact of ALGSA

Through initiatives like the ALGSA Collaborative Scientific Research Grant and partnerships with organizations such as Travere Therapeutics and NCATS/NIH, ALGSA is committed to advancing research and understanding of ALGS. The organization actively engages with scientists and researchers, creating opportunities for collaboration and community involvement.

Why Donate?

Your generous donations are crucial in providing educational materials, critical resources, and financial assistance to families navigating the challenges of Alagille Syndrome. Every contribution helps alleviate the emotional and financial burdens faced by these families.

Join the Cause

Support the Alagille Syndrome Alliance today by donating cryptocurrency or cash. Together, we can make a significant impact in the lives of those affected by ALGS and build a brighter future for all.