This is a fun post to write. As the title states NFNP is a finalist! I am so excited. By virtue of being a finalist many folks who have never heard of fibular hemimeila will now know it exists. Maybe folks who need resources will find them. Maybe some parent with a child with a limb difference that’s not necessarily fh will find this blog and know they are not alone.
When I began I wanted parents to be able to find information on FH and the limb lengthening reconstruction option. The web has come a long way and there are now many blogs by families with children with FH and even blogs by young adults with FH. I am in good company!
Please consider voting for No Fibula No Problem at the link below. You can vote once a day, every day through March 21.
Thanks to everyone who nominated us and thank you in advance for voting!