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.

Registration is OPEN for Virtualpalooza.  
Click HERE to visit the Virtualpalooza page see the full slate of events and to register!

 

Esperamos se unan a nosotros en el Virtualpalooza en el mes de julio - una serie de eventos virtuales de un mes de duración. Para ver los eventos que se estarán ofreciendo en julio, utiliza el siguiente enlace para traducir la página de Virtualpalooza a Espanol. 
haga clic aquí

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.

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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.