Little People of America

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!

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).

Little People of America is a primarily all-volunteer organization for persons and families involved with the condition of dwarfism. We do not diagnose, treat, or provide genetic counseling. We are involved in peer and parent support, medical resources and referrals, scholarships, and programs that benefit the dwarfism community, while promoting education, community outreach, personal and family strength, and life achievements.