Getting a diagnosis of clubfoot is hard. The treatment works but it takes a lot of effort. You shouldn’t have to feel like you’re going through this alone. We have a support group at POBAR for our clubfoot families. We meet every 2-3 months. The parents discuss tips and tricks about topics from keeping the braces on little feet to the emotional struggles that parents can feel when they are first diagnosed and later. They share practical information about where to inexpensively buy needed clubfoot items. We also talk about crucial information with the nurse practitioners including topics like clubfoot recurrences. Please join us if your child is affected with clubfoot. If you are interested email firstname.lastname@example.org or email@example.com.