We joined something like 600 other people today for the Down Syndrome Association of Middle Tennessee Spring Picnic at the Zoo. We did this last year – only it was a summer picnic then, and a lot hotter! – and it was so fun to see how much more Lina got out of the experience this year. My in-laws were able to join us, the weather was absolutely perfect, and the kids had a blast. We talked with plenty of families we know and met a few new ones.
We feel so lucky to have a local organization that offers these kinds of opportunities. We have landed in an amazing community, and these events carry such a palpable sense of acceptance and celebration. (A sort-of actual conversation Jon had: “You’re worried your kid will pull my kid’s hair? Hey, me, too! Maybe they’ll really go at it and cure each other!”) Parents of older kids pass down advice about IEP meetings, we stop to coo over the tiny newest members, we celebrate the recovery of kids who spent time in the hospital, we dance to MC Hammer and Taylor Swift, the kids eat too many cookies, we notice kids who look like older or younger versions of ours, we juggle plates and messes and tired little ones. It’s real and it’s joyful.
Everyone should get to experience a community like this.
Note: I wish I could share more pictures of this amazing group, but I don’t have releases to publicly post photos of other families and wouldn’t feel comfortable doing so without permission.