Our Son's Clubfoot Story : Plenty of Hope Ahead!
This video is not intended to show a false image of clubfoot as something easy or simple -- I realize many who were born with clubfoot a generation or more ago -- even just 15 years ago -- didn't necessarily have the same kind of treatment and may not have the same kinds of outcomes. I'm simply sharing our story of hope and our positive outcome because when you hear your child has a genetic birth defect, the first thoughts are of fear or sadness -- but we don't need to despair, we live in an amazing age and our little ones can get wonderful care! UPDATE: He is walking for real now! First steps: • Our Son's First Steps After Being Born Wit... Walking like a pro: • Jonas walking like a pro WELCOME & thanks for watching! We're just spreading the love & hope on World Clubfoot Day! Please keep in mind I am not a doctor, I'm just sharing one, individual story. But I'm happy to connect you to more qualified information and share a little hope! Read more about our journey with clubfoot on my blog: https://cartwheelingdowntheaisle.com/... An excellent resource for Clubfoot parents is https://www.clubfoothub.com And here is the official Ponseti website: http://www.ponseti.info Finally, here's a Facebook page to connect with other Clubfoot parents -- it's nice to know you're not alone! / clubfootmommas
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