Hi! this is my first time on this web site and i think it gives those of us with PFFD some great insight. I am 23 years old and was have bilateral pffd. I have not actually ever talked to anyone that has pffd. I live in Mississippi so if someone with pffd would share there story and information, i am actually going through the process of having a new prosthesis built and there are so many new things available.
Thanks, Hope