Welcome to Little People of America

Little People of America (LPA) is a nonprofit organization that provides support and information to people of short stature and their families.   LPA is only able to continue our work with support from members, friends and family.  Please consider making a donation today.

Benefits of Membership

Membership is available to individuals with a medical diagnosis of dwarfism or form of short stature, as well as their families, grandparents, relatives, and all medical professionals.  Benefits of membership include: peer, parent, and medical support at the chapter, regional and national level; discounted rates at the National conference; advocacy; LPA Today quarterly magazine; college scholarships and support; adoption and conference attendance grants; friendship and connections; referrals to medical care by dwarfism specialists; and general support for the dwarfism community.  

October is National Dwarfism Awareness Month

Help us spread positive information about dwarfism!  LPA challenges our membership to reach out to local schools, businesses, and organizations during the month of October and raise positive awareness about dwarfism. Our goal is to reach 10,000 people during the month. We will also have a daily posts about Dwarfism Awareness on our Facebook page, including LPA member photos and fun facts and a cool Teen Instagram program . Check it out each day and share on your own page! Purchase Dwarfism Awareness bracelets, pencils and information cards here.