Our Mission
Founded the program in loving memory of her daughter, Katerini Zoe Butler. Dr. Rores’s mission is to bridge gaps between families and providers, as well as, providing evidenced-based resources.
We are a grass-roots nonprofit started by a family within the community. Our mission is to support families within the Down syndrome community and others with medical diagnoses involving mental and/or physical delays in navigating medical uncertainty.
Katerini Zoe
Katerini Butler was a beautiful little girl and an important part of the Down syndrome community. In her brief time with us, Katerini made a huge impact on others. She was a bright shining light. Her infectious smile and sweet personality made a lasting impression on everyone she met.
In February 2022, with her parents by her side, precious Katerini passed away. To honor her daughter, Dr. Rores wants to give back to others in the community. Her mission is to help support families by working with health care providers to improve family-centered evidence-based care and to better understand the many facets of serving patients with Down syndrome or other mental and/or physical delays.
