Statement of Employment Support for People with Dwarfism
Little People of America (LPA) would like to extend its support to the plaintiffs in two Equal Employment Opportunity Commission (EEOC) lawsuits, both involving women with dwarfism. Employment discrimination remains a key issue in our community. LPA is dedicated to raising awareness around employment issues that face people with dwarfism and fully supports its members’ pursuit of any and all career opportunities.
Welcome to the new on-line home of Little People of America.
We hope you like our new look!
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 to our annual $50 for 50 More Years Fundraising Campaign.
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 on Regional and National conferences; 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.
LPA National Conference in San Diego
The 2014 National Conference in San Diego will take place July 4-10, 2014. Hotel and LPA Registration will begin April 1, 2014. Read and download and conference registration book here.