Is thers any one out there that has a child with pffd and club foot? If so could you please contact me as i would really love to hear from you,
We are thinking about going to America to America to see Dror Paley, and would like to know what we are in for also we have been told we can get her a prostesis that wont need surgery or one that will need surgery, we just really dont know what option to go for, Caoimhe is 21 months at the moment.
