Heather is the co-founder and current board member of the Down Syndrome Diagnosis Network, a national nonprofit that supports families with a Down syndrome diagnosis. As an advocate, Heather was integral in the passing of the Prenatal Trisomy Awareness Act which requires physicians to provide accurate information following a Trisomy 13, Trisomy 18 and Trisomy 21 diagnosis. She is the controller for a publishing company and is mom to three girls; her youngest, Izzy, has Down syndrome.
Abigail lives in Brooklyn Center with her parents, and has 8 siblings. She is actively engaged in activities with her peers with disabilities in church and elsewhere and enjoys reading, crafts, cooking and her work at Panera Bread. She loves being on the board of the Down Syndrome Association of Minnesota because she likes contributing ideas for activities and direction from the perspective of a self-advocate.
Christine is the founder of On Track MN and Potty Train MN, specialty consulting firms that provide consultation and training to individuals of all ages and their families. Offering more than twenty year of experience in behavior intervention and disability services, Christine has extensive training in Behavior Analysis and has worked in a variety of settings with a wide range of individuals including Autism Spectrum Disorder and Down syndrome. For the last six years, she and her husband have been live-in caretakers for two adults with Down Syndrome.
Cora Holland-Koller recently relocated back to Minnesota after living in St. Louis, Missouri for almost eight years where she and her husband, Damien Holler, were active with the Down Syndrome Association of Greater St. Louis. Cora is the Loan Agency Transaction Team Manager at SRS Acquiom, a financial services firm. She has two children; her youngest has Down syndrome.
Toni is married and has one son, Matthew, who has Down syndrome and is the light of her life. Since Matthew’s birth, she has been passionate about advocating for those with special needs, volunteering on committees such as school district's Special Education Advisory Council, the Gillette Specialty Healthcare Clinic’s Family Advisory Council and Family Voices of MN Parent to Parent program, plus is active in the Disability Public Policy initiatives.
Laura is a former board member, Duluth Buddy Walk coordinator, and most recently DSAMn’s Regional Coordinator for Northern Minnesota. In addition to her involvement with DSAMn, Laura is an accomplished photographer and is the founder of Project Joy, a nonprofit addressing childhood hunger in her community. Laura is from Duluth and is the mother to Jonah, young man with Down syndrome.
Gina has a diverse background as an advocate, community leader, and personal trainer. She is a graduate of Partners in Policymaking and is passionate about speaking to the opportunities and challenges that outdated laws present for individuals with disabilities. Gina is the mom to three; her middle child, Gunnar, has Down syndrome.
Kari has been an avid DSAMn volunteer for the last several years. In addition to her involvement with DSAMn, Kari is very involved with Special Olympics and is the Lakeville Baseball Association’s Miracle League Director. Dani retired in 2018 after a 30 year career with the Minneapolis Police Department. Kari is from Elko New Market and is the mother to Dani, a young woman with Down syndrome.
Heidi Berry Sturman
Heidi Berry Sturman is a mother of three active girls; her eldest is a young adult with Down syndrome. Employed in finance by a biomedical device company, she is a passionate fan of Wayzata‘s Lakers, Blues Top Soccer, the MN Vortex Fastpitch and Wayzata Fastpitch Softball teams.
Christopher is a Logistics Manager with General Mills. He and his wife, Brittany, are parents to Weston, age 1, who has Down syndrome. In the summer, you'll find him and his family up at their cabin or on the lakes of Minnesota.