Galactosemia Foundation is a non-profit organization based in Albany, NY that focuses on raising awareness and providing support for individuals affected by galactosemia, a rare genetic disorder. The foundation offers resources and educational materials to help those living with galactosemia navigate their condition and improve their quality of life.
Through community outreach and advocacy efforts, Galactosemia Foundation strives to promote research and advancements in the field of galactosemia, while also fostering a supportive network for individuals and families impacted by the disorder. By working collaboratively with healthcare professionals and researchers, the foundation aims to enhance understanding and treatment options for those affected by galactosemia.
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