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Our events are creating spaces for local communities to come together and experience fellowship with people with and without Down syndrome. They are an opportunity to celebrate the gift that is Down syndrome and foster belonging within the community.

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Our advocacy works to show what life with Down syndrome is really like by partnering with self advocates. The only people who know what it's like to have Down syndrome are people who actually have Down syndrome, so we want to make space to listen to their experiences.

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Our comfort boxes are sent to children with Down syndrome who are in the midst of serious medical challenges. Children who qualify for this program must have Down syndrome and a serious medical condition that has required treatment within the past or upcoming 3 months.

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"I cannot thank you enough for taking a moment in this busy life to extend support to a fellow baby of your community! Townes was elated and I even more. We felt overwhelmed with support. I just wanted to thank any and all partners who make these wonderful memories happen. We are so appreciative and grateful for your support and care. We can’t believe how beautiful this community truly is."

One of the characteristics of Down syndrome is Brushfield spots, small white spots in the iris. These spots don't impact a person's vision, and they don't actually have a purpose besides looking beautiful! While not every personal with Down syndrome will have Brushfield spots, they are much more common in people with Down syndrome. They are whimsical and enchanting, so we wanted to celebrate our favorite characteristics of Down syndrome by using Brushfield in our name!

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"When I was 15 years old, I felt the call on my heart to take my passion for people with Down syndrome a step further by starting a nonprofit organization. I wanted to be obedient to what God was calling me to do in giving back to the community that He used to bring my life so much purpose."

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