From the author, Angela Williams:

‘What do you know about Club Feet?’

The echo of those words will never leave me. This is how we found out our daughter would be born with a birth defect.

Tears.

All I heard was our baby girl wasn’t perfect. I imagined a wheelchair. Long metal braces. Would she even walk?

The casts [our daughter had to wear] were harsh looking. Rough. Baths were tricky and I knew when she cried it could be that her skin was itching… and that I couldn’t help her. Five weeks crawled by and the final set of casts were removed. Her feet… were beautiful. [But] the hardest part was next: successful permanent correction would require diligent, long-term wearing of a Ponseti brace. All day. Every day. For years. But what else could I do? How could I help her beyond that time? What if she were to have a child someday with…gulp…an issue? How could I monumentally make a difference for her as a mother?

I had an idea. A story.

It would be our mark: A book.

Donate today and receive your very own copy of this heartwarming book for parents, grandparents, and other people in your child’s life to ease understanding of clubfeet and the Ponseti Method of treatment.