Each October, the non-profit advocacy organization called Little People of America (LPA) leads communities around the globe in celebrating Dwarfism Awareness Month, a time dedicated to increasing public knowledge and understanding of dwarfism and the challenges faced by individuals with short stature. It is also a time for Little People to share their pride about having dwarfism and being part of LPA. In this blog post, I will explore the mission of LPA, the significance of Dwarfism Awareness Month, and how both advocate for the inclusion of LPs in society.

I am proud to say that I have been a member of LPA for almost 20 years. Because of my scoliosis and other related orthopedic conditions, I am 4’ tall. I learned about the organization from one of my best friends, Robyn, who is a Diastrophic Dwarf. It has been a wonderful community to be a part of. I like to think that I would have met my husband because we are “meant to be.” But the fact is, that LPA had a part in that, too. Robyn met Drew, who is also an LP, at a LPA National Conference that I was not able to attend. She introduced us after she got home. And the rest, they say, is history.

LPA was founded in 1957 by actor Billy Barty, who was a dwarf with Achondroplasia. Since its founding, LPA has grown into the foremost advocacy organization for individuals with dwarfism in the United States. There are also several chapters around the world. It was established as a support network and has evolved into a multifaceted entity focusing on medical support, scholarships, public awareness, and advocacy. With over 6,000 members, LPA provides a vibrant community that addresses the many aspects of living with dwarfism, including medical issues, disability rights, and personal development.

LPA’s mission is dedicated to improving the quality of life for people with dwarfism throughout their lives while celebrating with great pride Little People’s contribution to social diversity.  LPA strives to bring solutions and global awareness to the prominent issues affecting individuals of short stature and their families.

In addition to educational efforts, LPA is deeply involved in advocacy work, promoting fair and equal treatment in areas such as healthcare, employment, and accessibility. The organization also provides scholarships to members pursuing higher education and financial assistance for medical procedures related to dwarfism that are often not covered by insurance.

THE IMPORTANCE OF DWARFISM AWARENESS MONTH

Dwarfism Awareness Month, observed every October, plays a crucial role in LPA’s mission to educate the public. Despite advancements in societal inclusion, misconceptions about dwarfism remain widespread. Dwarfism Awareness Month helps educate the public on what dwarfism is — a medical or genetic condition that results in an adult height of 4 feet 10 inches or shorter. The most common form of Dwarfism is a condition called Achondroplasia.

This month of advocacy also provides a platform to explain the correct terminology (the term "midget" is considered offensive and inaccurate) and to encourage respectful and informed interaction with individuals with dwarfism. Another one of LPA’s concerted public awareness campaigns has been around stopping dwarf tossing. Dwarf tossing is a degrading and harmful activity that involves throwing Little People for entertainment. This practice not only promotes ableism and disrespect towards individuals with dwarfism but also puts their physical well-being at significant risk.

This month also serves as a rallying point to advocate for the rights of people with dwarfism. LPA utilizes this time to push for advancements in policy concerning disability rights and inclusion, ensuring that individuals with dwarfism have equal opportunities in education, employment, and social participation. It is also an opportunity to celebrate the contributions of individuals with dwarfism in various fields such as sports, arts, science, and public service. Highlighting these achievements challenges existing stereotypes and demonstrates that individuals with dwarfism lead rich, productive lives.

Lastly, for many individuals with dwarfism and their families, Dwarfism Awareness Month is a time to connect with others who share similar experiences. Through events and social media campaigns, people are able to share stories, offer support, and strengthen their sense of community.

HOW TO PARTICIPATE AND SUPPORT DWARFISM AWARENESS MONTH

• Take time to learn about dwarfism, using resources provided by LPA and other reputable sources. Share this knowledge with friends, family, and colleagues to help spread awareness.

• Attend public events or virtual webinars hosted by LPA. These are great opportunities to learn directly from experts and individuals with dwarfism.

• Advocate for inclusive policies in your community, workplace, or school. Ensure that individuals with dwarfism are considered in diversity and accessibility planning.

• Consider donating to Little People of America or volunteering your time. Financial and volunteer support are crucial for LPA to continue its valuable work. For more information and/or to donate, go to LPA’s website at www.lpaonline.org.