Be sure to check your local chapter and district websites for events! LPA is a membership organization and most events are only open to individuals with dwarfism and their families. Have a question? Contact the office at email@example.com or your local chapter or district for more information. Click here for a current list of Spring 2015 Regional Meetings and events.
What is LPA?
Little People of America, Inc., is a national nonprofit organization that provides support and information to people of short stature and their families.
Short stature is generally caused by one of the more than 200 medical conditions known as dwarfism. LPA welcomes all 200+ forms of dwarfism.
LPA has more than 6000 members across the United States and internationally. We have 13 districts and 70 chapters.
LPA provides social interaction, parent and peer support, medical support and education, scholarships and grants. Our members range from newborns to senior citizens, little people and average height. Dwarfism cuts across all religions, ethnicities, and economic levels. All are welcome!
Where We Began
In 1957, well-known actor Billy Barty made a national public appeal for all little people in America to join him for a gathering in Reno, Nevada. Mr. Barty and 20 other little people joined together and Little People of America was formed!
What We Do
LPA offers information on employment, education, disability rights, adoption, medical issues, clothing, adaptive products, and the many stages of parenting a short-statured child - from birth to adult. Information is provided through a national newsletter, the LPA Today, and numerous seminars and workshops which occur locally at chapter events, regionally at District Meetings, and nationally at our yearly national conference.