My Ledderhose story

By Bashan, Ledderhose disease, United States, March 7, 2019

I found out I had Ledderhose in 2011. Mine are primarily in my heels. I was told the only surgical option was to have the fascia removed from the bottom of my feet. Not an option. The other is wear wedge heels. The option. Also this disease used to be called clap feet. 

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