Recently, I had the opportunity to attend the GiGi’s Playhouse Gala, and I am always so grateful to be part of an evening that carries so much meaning for the Down syndrome community.
GiGi’s Playhouse provides so many purposeful programs, resources, and opportunities for individuals with Down syndrome and their families, and one of the things that makes those programs so special is that they are offered free of charge to families. Events like the gala play an important role in helping make that possible. They bring people together who believe in creating a more accepting, inclusive, and supportive world for individuals with Down syndrome while also raising the funds needed to continue providing these incredible programs.
This gala was especially meaningful because my parents were able to attend with me. It was actually my dad’s first GiGi’s Playhouse Gala! He typically stays home to watch Kay because finding a sitter who is comfortable and capable of managing Kay’s diabetes can be challenging. This time, we were fortunate enough to have one of Kay’s RBTs from her ABA facility available to spend the evening with her. She already knows Kay, understands her diabetes, and was someone we felt completely comfortable leaving her with, which made it possible for my parents to join us and enjoy the evening too. Having that extra support made it possible for my parents to join us and enjoy the evening too.
Our family and friends were also able to contribute to the evening in some really special ways. A family friend created an absolutely beautiful quilt specifically to donate to the silent auction in honor of Kay. It was personalized as “The 2026 Kay Quilt,” along with the maker’s name and other meaningful details. Knowing that someone took the time and care to create something so beautiful in honor of Kay, and then chose to donate it to help support GiGi’s Playhouse, was incredibly touching.
My mom also put together an amazing art-themed basket for the silent auction. She filled it with art supplies, books about creating art, and some of her own creations from her art business, including stickers, postcards, and other fun items. There was something for someone just beginning to explore painting, as well as plenty for someone who already loves to create and wanted to add to their collection. It was such a fun way for her to share her love of art while also supporting an organization that means so much to our family.
There is something really special about being in a room filled with people who are all there for the same reason. Whether they have a loved one with Down syndrome, work within the community, support the mission, or simply believe in making a difference, everyone comes together to celebrate the people at the heart of it all.
For our families, having organizations like GiGi’s Playhouse matters. These programs create opportunities to learn, grow, build friendships, develop independence, and connect with other families who understand the journey. They remind families that they are not alone and that there is an entire community cheering them on.
Gala events like this also give the community a chance to look beyond the fundraising itself and celebrate how far we have come, recognize the people who continue to make a difference, and remember why this work matters so much. Every person who attends, donates, sponsors, volunteers, or simply shares the mission helps contribute to something much bigger than one evening.
I was especially happy to have Trina and Britt there with us. Having the opportunity to share an evening like this with people who are also so connected to and passionate about our community made the night even more special.
I am incredibly grateful for organizations like GiGi’s Playhouse and for the people who continue to show up for the Down syndrome community. It truly takes a community to create meaningful change, and nights like this are such a beautiful reminder of what can happen when that community comes together.
Here’s to continuing to celebrate, support, and create opportunities for individuals with Down syndrome and their families.