About Us

About Our Organization

Founded in 1987, the Down Syndrome Organization of Southern Nevada (DSOSN) is a 501(c)(3) organization with a service population made up of individuals with unique abilities, most of whom are diagnosed with Down syndrome and other intellectual developmental disabilities (I/DD). The organization offers an array of impactful programs and recreational activities, all at no cost to its members. Aimed at meeting the critical needs of this service population, DSOSN also fosters a constructive perception of persons diagnosed with Down syndrome (and other I/DD) by focusing on maximizing their potentials, through self-awareness, self-advocacy, inclusion, and job-readiness preparation, with all their programs and training rooted in the following three Core Pillars: Education, Employment, and Independent Living.

For questions and/or additional information, you may also contact Peter Whittingham, Chair, Board of Directors, at the phone number or email address below:

P: (626) 780-5976
E: pwhittingham@dsosn.org

DSOSN is a 501(c)(3) non-profit organization and a primary source of support, information and education for new families affected by Trisomy-21.

We are members of the Las Vegas Chamber of Commerce and collaborate with other agencies that provide services to people with special abilities.

Our Mission

To enlighten the public by promoting a positive understanding of Down syndrome in the community and be a source of support, information, and education for families and individuals with Down syndrome.

Bylaws

What is Down Syndrome?

Down syndrome is a genetic condition that occurs once in every 691 births. It is the most frequently occurring chromosomal condition and is found in people of all races and economic levels. More than 400,000 people in the United States have Down syndrome.

A few of the common physical traits of Down syndrome are low muscle tone, small stature, an upward slant to the eyes, and a single deep crease across the center of the palm. Every person with Down syndrome is a unique individual and may possess these characteristics to different degrees or not at all.

People with Down syndrome have an increased risk for certain medical conditions such as congenital heart defects, respiratory and hearing problems, Alzheimer’s disease, childhood leukemia, and thyroid conditions. However, many of these conditions are now treatable, so most people with Down syndrome lead healthy lives. Life expectancy for people with Down syndrome has increased dramatically in recent decades – from 25 years old in 1983 to 60 years old today.

People with Down syndrome experience cognitive delays, but the impact is usually mild to moderate and is not indicative of the many strengths and talents that each individual possesses. Children with Down syndrome learn to sit, walk, talk, play, and do most other activities; only somewhat later than their peers without Down syndrome.

Quality educational programs, a stimulating home environment, good health care, and positive support from family, friends and the community enable people with Down syndrome to develop their full potential and lead fulfilling lives. People with Down syndrome attend school and work, and participate in decisions that concern them, and contribute to society in many wonderful ways.

Community Partners & Supporters

Additional Resources