Little People of America (LPA) is a national nonprofit organization founded in 1957 that provides support and information to individuals with dwarfism and their families. The organization aims to improve the quality of life for people with dwarfism through advocacy, education, and community support. LPA also works to raise awareness about dwarfism and to promote acceptance and understanding within society. Over the years, LPA has organized numerous events, including national conferences, to foster a sense of community among its members and to provide resources for navigating challenges related to dwarfism.
LPA's mission includes advocating for the rights of individuals with dwarfism, providing educational resources, and facilitating social connections among members. The organization also engages in outreach efforts to educate the public about dwarfism and to combat stereotypes and misconceptions. LPA has grown significantly since its inception, now serving thousands of members across the United States and beyond, and continues to be a vital resource for individuals and families affected by dwarfism.