CLUBFOOT

Who are we?

Clubfoot C.A.R.E.S. is a US-based, nonprofit advocacy group created by moms who have children with clubfoot. We promote public awareness of clubfoot and the Ponseti method of treatment, and we work to educate and empower patients and their families.  

What do we want to do?

Our immediate goals are:

  • To educate the public about the condition clubfoot, thus creating more awareness and eradicating stigmas.

  • To bring awareness to the Ponseti method as the preferred non-surgical treatment.

  • To advocate for clubfoot patients and parents of children with clubfoot.

Want to help?
Want to help?

Please email us! We'd love to hear from you!

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Are you a new Clubfoot parent?
Are you a new Clubfoot parent?

Please check out our "parent" page! We are also here to talk and guide you through the process. Please send us an email and we can help you navigate your new journey!

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Blisters from Bracing?
Blisters from Bracing?

We can help! Check out our page on bracing for blister help.

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CLUBFOOT STORIES

My son was diagnosed at 20 weeks in utero. I was told over and over that it would be an 'easy fix' and that I 'wouldn't even remember it happened.' But, here I am. My son's foot is atypical and I wake up every morning hoping he hasn't relapsed.” 

 

—  Nicole, Co-founder of Clubfoot C.A.R.E.S.