For Vollbrachts, supporting Global is a family investment
For Bill and Leslie Vollbracht, supporting the Global Down Syndrome Foundation is a family investment in their granddaughter and others who have Down syndrome.
Seasoned entrepreneurs, the Vollbrachts are betting on Global’s research, medical care and outreach. They recently sat down with Global to talk about Colorado, family and why support for Down syndrome medical care and research is so important.
1. You founded and built Land Title Guarantee Company, one of the oldest and most successful title insurance companies in Colorado. What was it like to be a Colorado pioneer?
2. How do you apply your business background to your philanthropic giving?
3. Your granddaughter Katherine Vollbracht Winfield happens to have Down syndrome. How has she changed your lives?

4. How important was the Global Down Syndrome Foundation and the Sie Center for Down Syndrome at Children’s Hospital Colorado for Katherine’s development?
5. How do you feel about your daughter and son-in-law managing the information age, work, children, and becoming advocates for people with Down syndrome?
6. What do you want people to know about Katherine?
7. What is the best thing about being a grandparent?
8. You are part of the Leadership Circle supporting Global’s marquee fundraiser and awareness-raiser – the Be Beautiful Be Yourself Fashion Show. Why should people support and attend this event?
9. What is the best advice you were ever given that you would like to pass on?
Recent Posts
- Happy Thanksgiving from Our GLOBAL Team: Thank You for Being Part of Our Family
- “They Came to Us!” Nebraska Mom Shares Family’s Research Experience
- Hollywood Stars, Advocates and Models with Down Syndrome Shine at GLOBAL’s Be Beautiful Be Yourself Fashion Show
- Jessica Biel Joins Star-Studded Lineup to Support Global Down Syndrome Foundation During Awareness Month
- Exclusive Interview with Black Down Syndrome Association Co-Founders Kelli Caughman & Crystal Lotterberry
Experience our inspirational and groundbreaking videos and photos. Our children and self-advocates are beautiful AND brilliant!
Make sure your local Representatives are on the Congressional Down Syndrome Task Force.