What is LPA?

Little People of America, Inc., is a national non-profit organization that provides support and information to people of short stature and their families.  We are the only dwarfism support organization that includes all 200+ forms of dwarfism.  

Short stature is generally caused by one of the more than 200 medical conditions known as dwarfism.

LPA has more than 6000 members across the United States and internationally. We have 14 districts and 70 chapters.  

LPA provides social interaction, parents and peers 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!

Click here to read a wonderful article on LPA's first 50 years - 1957-2007.

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. 

LPA also provides opportunities for social interaction as well as participation in athletic events through our sister organization, the Dwarf Athletic Association of America (DAAA).