The Ryan Foundation for MPS Children is a non-profit organization based in Carrollton, TX, dedicated to funding scientific research and finding treatments for rare diseases, particularly Mucopolysaccharidosis (MPS) and other Lysosomal Storage Diseases (LSD). They work closely with legislators and researchers to build partnerships and advocate for the rare disease community, aiming to improve the quality of life for individuals and families affected by these conditions.
With a focus on diseases that receive little to no research due to their rarity, the Ryan Foundation aims to provide hope and support to children and families facing the devastating impact of rare diseases. They rely on personal donations to fund specific scientific projects that can lead to life-saving treatments, striving to create a better future for those currently living with rare diseases and future generations.
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