Our vision is to see people with Down syndrome living meaningful lives as productive members of their communities throughout all stages of life by increasing awareness, promoting acceptance and advancing advocacy.
Down Syndrome Alabama started in June of 1987 as a group of dedicated parents who wanted to advocate for their children who had Down syndrome. They incorporated under the name PADS (Parent Advocates Down Syndrome) and started this organization.
April 23, 2013
In August of 2012, the Board of Directors made and seconded a motion that the name of the organization be permanently changed to Down Syndrome Alabama. And on April 23, 2013 the amendment was filed and the organization officially changed it's name.
In the new year of 2020, Down Syndrome Alabama elected new board members and hired a new Executive Director in the hopes that we can move the organization forward to become a leading champion in our state for those living with Down syndrome.
Kelly Peoples has worked in non-profit in the Birmingham area since 2001 and brings knowledge of development, marketing, and management. She was excited to join Down Syndrome Alabama in January 2020 as DSA builds on past successes to implement a plan of strategic growth in programs, outreach, development, and membership. Peoples received her degree in Public Relations from Auburn University. She and her husband Greg live in Hoover, AL with their three children.
BOARD OF DIRECTORS
Board of Directors, President
Stephanie joined the Board of Directors in January 2020. She provides 15 years of experience in business along with 8 years of working in marketing and communications. Her involvement and volunteer work with Down Syndrome Alabama started in 2012 when her son was born and diagnosed with Down syndrome. Her passion to help others on their DS journey is what lead her to take on a leadership role. She and her husband Rob live in Trussville with their son Zac.
Board of Directors, Vice President
Katherine Gorham got involved with DSA through the Learning Program in 2013. Two years later, she helped develop and administer a two day, statewide education conference. After the sucess of the conference, she worked to implement an Education division for DSA to provide resources to educators in our area. She is actively involved in her local PTO and currently sits on the Vestavia Hills Parks and Recreation Foundation Board and the Help the Hills Coalition Board. She joined the DSA Board in January of 2020 as the Treasurer. She lives in Vestavia Hills with her husband, Bob, and is mother to five children. Her youngest, Nate, who has Down syndrome, is the inspiration and drive for her advocacy through DSA.
Board of Directors, Secretary
Corrie and her husband, Jason, have been members of DSA since 2009 when their son George was born. In 2013, Corrie worked alongside other members to bring the Down Syndrome Foundation of Orange County’s Learning Program to DSA. She also serves on the state’s Special Education Advocacy Panel (SEAP) and Protection & Advocacy for Individuals with Developmental Disabilities (PADD). Corrie joined the DSA board in the hope that her advocacy will encourage others on their journey. She has a deep appreciation for the many DSA mentors who inspired and supported her. Corrie is an alum of Auburn University and lives with her family in Trussville.
Board of Directors, Treasurer
Jamie joined the Board of Directors in January 2020. He graduated from Huntingdon College in Montgomery, AL with degrees in Accounting and Economics/Finance. He holds the Certified Internal Auditor (CIA) and Certified Financial Services Auditor (CFSA) designations. He comes to DSA with 23 years of experience in various roles in audit and accounting. His goal is to see DSA continue to be a trusted partner and resource for families on the Down Syndrome journey. He and his wife Ashley live in Vestavia Hills with their two boys Andrew and Matthew.
Dr. John Cortopassi, MD
Dr. Snehal Khatri, MD
Mary Meadows Livingston
Dr. Christina Norman
Marcella Roberts, Esq., Past President