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.

LPA's 2019 Annual Report & Special Edition LPA Today
Click on images below to view our 2019 Annual Report and accompanying Special Edition LPA Today

LPA 2019 Annual Report         Special Edition LPA Today

2020 LPA Conference Information
The LPA Conference Management Committee is busy finalizing plans for the 2020 National Conference in the ever amazing city of Austin, Texas. Spend the week with us in the Lone Star State and join your LPA friends at the JW Marriott in downtown Austin, July 3 - July 10!  
LPA Registration and JW Marriott Reservations open Wednesday, April 15. 
For more information and a peek into the week, click here

JW Marriott in the heart of downtown Austin  JW Marriott Pool in Austin, TX

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; monthly eNewsletter, 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.



LPA Members were asked, "What does LPA mean to you?" This word cloud was created from the responses. Words are scaled in accordance with how many times they were mentioned. The full results of our membership survey can be seen here.